Unidentified gut microbes |
Baicalin |
Herbal Substance |
Medicinal Herbal Compounds |
Hydrolysis; deglycosylation |
Baicalein; oroxylin A |
Increase Efficacy |
n.a. |
Inflammation; diabetes mellitus; tumor |
n.a. |
Increased activity |
PMID: 26569070; PMID: 22516259; PMID: 24947972; PMID: 24033282
|
Unidentified gut microbes |
Olsalazine |
Therapeutic Substance |
Approved Drug |
Azo reduction |
5-aminosalicylclic acid |
Increase Efficacy; Increase Toxicity |
n.a. |
Inflammatory diseases(ulcerative colitis; Crohn’s disease; rheumatoid arthritis) |
n.a. |
Increased activity or causing side effects(anorexia and nausea) |
PMID: 26569070; PMID: 11230497
|
Unidentified gut microbes |
Nizatidine |
Therapeutic Substance |
Approved Drug |
N-oxide bond cleavage |
n.a. |
Decrease Efficacy |
n.a. |
Peptic ulcer disease |
n.a. |
Decreased intestinal absorption and systemic bioavailability |
PMID: 26569070; PMID: 13481854
|
Unidentified gut microbes |
Ranitidine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
N-oxide bond cleavage |
n.a. |
Decrease Efficacy |
n.a. |
Peptic ulcer disease |
n.a. |
Decreased intestinal absorption and systemic bioavailability |
PMID: 26569070; PMID: 13481854
|
Unidentified gut microbes |
Flucytosine |
Therapeutic Substance |
Approved Drug |
Deamination |
5-fluorouracil |
Increase Efficacy; Increase Toxicity |
n.a. |
n.a. |
n.a. |
Increased activity or toxicity |
PMID: 26569070; PMID: 14768038
|
Unidentified anaerobic bacterium |
Sulfinpyrazone |
Therapeutic Substance |
Approved Drug |
Reduction |
sulindac sulfide; sulinpyrzone sulfide |
Increase Efficacy |
n.a. |
n.a. |
n.a. |
Increased activity |
PMID: 26569070; PMID: 18927500
|
Unidentified anaerobic bacterium |
Sulindac |
Therapeutic Substance |
Approved Drug |
Reduction |
sulindac sulfide; sulinpyrzone sulfide |
Increase Efficacy |
n.a. |
n.a. |
n.a. |
Increased activity |
PMID: 26569070; PMID: 18927500
|
Unidentified gut microbes |
Insulin human |
Therapeutic Substance |
Approved Drug |
Proteolysis |
Peptides |
Decrease Efficacy |
n.a. |
Type 1 diabetes mellitus |
n.a. |
Decreased activity |
PMID: 26569070; PMID: 21051639
|
Unidentified gut microbes |
Loperamide oxide |
Therapeutic Substance |
Investigational Drug |
Reduction |
Loperamide |
Increase Efficacy |
n.a. |
n.a. |
n.a. |
Increased activity |
PMID: 26569070; PMID: 21148486
|
Unidentified gut microbes |
Nitrazepam |
Therapeutic Substance |
Approved Drug |
Nitroreduction |
7-aminonitrazepam |
Increase Toxicity |
n.a. |
Moderate to severe insomnia |
n.a. |
Inducing teratogenicity |
PMID: 26569070; PMID: 21156650
|
Unidentified gut microbes |
Nitroglycerin |
Therapeutic Substance |
Approved Drug |
Denitration |
Glyceryl-1,3-dinitrate; glyceryl-1,2-dinitrate; glyceryl-1-mononitrate; glyceryl-2-mononitrate |
Decrease Efficacy |
n.a. |
Angina pectoris |
n.a. |
Decreased activity |
PMID: 26569070; PMID: 22902524
|
Unidentified gut microbes |
Dihydroxyphenylalanine (DOPA) |
Therapeutic Substance |
n.a. |
Dehydroxylation |
m-tyramine; m-hydroxylphenylacetic acid |
Increase Efficacy |
n.a. |
Parkinson’s disease |
n.a. |
Increased activity |
PMID: 26569070; PMID: 24264989
|
Unidentified gut microbes |
Indomethacin |
Therapeutic Substance |
Approved Drug |
Deconjugation |
n.a. |
Decrease Efficacy; Increase Toxicity |
n.a. |
n.a. |
n.a. |
Decreased activity; increased side effects(diarrhea; anorexia; weight loss) |
PMID: 26569070; PMID: 24264990
|
Unidentified gut microbes |
Simvastatin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
Hydrolysis; demethylation; hydroxylation/dehydroxylation; β-oxidation |
Lactic acid; 3-hydroxybutanoic acid; cyclohexanecarboxylic acid; 2-hydroxyvaleric acid |
n.a. |
n.a. |
Cardiovascular disease |
n.a. |
Altering its lipid-lowering activity |
PMID: 26569070; PMID: 5913083
|
Unidentified gut microbes |
Risperidone |
Therapeutic Substance |
Approved Drug |
Ring cleavage; hydroxylation |
Benzisoxazole ring scission; Benzisoxazole ring hydroxylation |
Increase Toxicity |
n.a. |
n.a. |
n.a. |
Inducting symptoms of Parkinson’s disease |
PMID: 26569070; PMID: 6836275
|
Unidentified gut microbes |
Chloramphenicol |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
Amine formation; hydrolysis |
p-aminphenyl-2-amino-1; 3-propanediol |
Increase Toxicity |
n.a. |
n.a. |
n.a. |
Inducing bone marrow aplasia |
PMID: 26569070; PMID: 8706020
|
Clostridium sp. |
Daidzein |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
Reduction; phenolic ring opening |
Dihydrodaidzein; equol; O-desmethylanolensin(ODMA) |
Increase Efficacy |
n.a. |
Osteoporosis; menopausal symptoms; cardiovascular diseases; obesity |
n.a. |
Increased activity |
PMID: 26569070
|
anaerobic bacterium 'strain 7' |
Daidzein |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
Reduction; phenolic ring opening |
Dihydrodaidzein; equol; O-desmethylanolensin(ODMA) |
Increase Efficacy |
n.a. |
Osteoporosis; menopausal symptoms; cardiovascular diseases; obesity |
n.a. |
Increased activity |
PMID: 26569070
|
Bacteroides uniformis |
Genistein |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
Hydrogenation |
Production of 5-hydroxyequol |
n.a. |
n.a. |
Obesity; type 2 diabetes |
n.a. |
n.a. |
PMID: 26569070
|
Bacteroides |
Ginsenoside Rb1 |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
Hydrolysis |
Compound K |
Increase Efficacy |
n.a. |
Inflammation; tumor |
n.a. |
Increased activity |
PMID: 26569070
|
Bifidobacterium |
Ginsenoside Rb1 |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
Hydrolysis |
Compound K |
Increase Efficacy |
n.a. |
Inflammation; tumor |
n.a. |
Increased activity |
PMID: 26569070
|
Eubacterium sp. GLH |
Glycyrrhizin |
Herbal Substance |
Medicinal Herbal Compounds |
Hydrolysis |
18-β-glycyrrhetinic acid |
Increase Efficacy |
n.a. |
Inflammation |
n.a. |
Increased activity |
PMID: 26569070
|
Pseudocera |
Hesperidin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
Deglycosylation |
Hesperetin |
Increase Efficacy |
n.a. |
n.a. |
n.a. |
Increased activity |
PMID: 26569070
|
Klebsiella pneumoniae |
Lactulose |
Therapeutic Substance |
Approved Drug |
Hydrolysis |
Monosaccharides; lactate, acetate; butyrate |
n.a. |
n.a. |
n.a. |
n.a. |
Stimulating the growth of beneficial bacteria(Bifidobacteria; Lactobacilli) |
PMID: 26569070
|
Enterococcus faecalis |
Lactulose |
Therapeutic Substance |
Approved Drug |
Hydrolysis |
Monosaccharides; lactate, acetate; butyrate |
n.a. |
n.a. |
n.a. |
n.a. |
Stimulating the growth of beneficial bacteria(Bifidobacteria; Lactobacilli) |
PMID: 26569070
|
Cronobacter sakazakii |
Lactulose |
Therapeutic Substance |
Approved Drug |
Hydrolysis |
Monosaccharides; lactate, acetate; butyrate |
n.a. |
n.a. |
n.a. |
n.a. |
Stimulating the growth of beneficial bacteria(Bifidobacteria; Lactobacilli) |
PMID: 26569070
|
Enterococcus casseliflavus |
Lactulose |
Therapeutic Substance |
Approved Drug |
Hydrolysis |
Monosaccharides; lactate, acetate; butyrate |
n.a. |
n.a. |
n.a. |
n.a. |
Stimulating the growth of beneficial bacteria(Bifidobacteria; Lactobacilli) |
PMID: 26569070
|
Bacteroides |
Levamisole |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
Thiazole ring opening |
levametabol-I; levametabol-II; levametabol-III |
Increase Efficacy |
n.a. |
Colon cancer |
n.a. |
Increased activity |
PMID: 26569070
|
Clostridium sp. |
Levamisole |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
Thiazole ring opening |
levametabol-I; levametabol-II; levametabol-III |
Increase Efficacy |
n.a. |
Colon cancer |
n.a. |
Increased activity |
PMID: 26569070
|
Clostridia |
Metamfetamine |
Therapeutic Substance |
Approved Drug |
Demethylation |
Amphetamine; norephedrine; an unknown metabolite |
Decrease Efficacy |
n.a. |
n.a. |
n.a. |
Decreased activity |
PMID: 26569070
|
Enterococcus |
Metamfetamine |
Therapeutic Substance |
Approved Drug |
Demethylation |
Amphetamine; norephedrine; an unknown metabolite |
Decrease Efficacy |
n.a. |
n.a. |
n.a. |
Decreased activity |
PMID: 26569070
|
Lactobacillus |
Metamfetamine |
Therapeutic Substance |
Approved Drug |
Demethylation |
Amphetamine; norephedrine; an unknown metabolite |
Decrease Efficacy |
n.a. |
n.a. |
n.a. |
Decreased activity |
PMID: 26569070
|
Unidentified anaerobic bacterium |
Omeprazole |
Therapeutic Substance |
Approved Drug |
Reduction |
corresponding sulfide metabolites |
Decrease Efficacy |
n.a. |
Gastric ulcer |
n.a. |
Decreased activity |
PMID: 26569070
|
Enterococcus casseliflavus |
Quercetin-3-glucoside |
Herbal Substance; Dietary Substance |
Medicinal Herbal Compounds; Dietary Compounds |
Deglycosylation |
Butyrate; acetate; 3,4-dihydroxyphenylacetic acid |
n.a. |
n.a. |
Cardiovascular disease; tumors |
n.a. |
n.a. |
PMID: 26569070
|
Eubacterium ramulus |
Quercetin-3-glucoside |
Herbal Substance; Dietary Substance |
Medicinal Herbal Compounds; Dietary Compounds |
Deglycosylation |
Butyrate; acetate; 3,4-dihydroxyphenylacetic acid |
n.a. |
n.a. |
Cardiovascular disease; tumors |
n.a. |
n.a. |
PMID: 26569070
|
Clostridioides difficile |
Acetaminophen |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
O-Sulfation; C-S cleavage of acetaminophen-3-cysteine |
acetaminophen sulfate; glucuronide |
Increase Efficacy; Decrease Toxicity |
n.a. |
n.a. |
Microbial product(p-cresol) could alter the ratio of metabolites |
Altered activity or toxicity |
PMID: 26569070
|
Eggerthella lenta |
Digoxin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
Reduction |
Dihydrodigoxin; dihydrodigoxigenin |
Decrease Efficacy |
Human |
Heart disease |
n.a. |
Decreased cardiac activity |
PMID: 26569070
|
Unidentified gut microbes |
Levodopa |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
Dehydroxylation |
m-tyrosine; m-tyramine; m-hydroxyphenylacetic acid |
Decrease Efficacy |
n.a. |
Parkinson's disease |
n.a. |
Decreased activity |
PMID: 26569070
|
Unidentified gut microbes |
Metronidazole |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
Reduction |
N-(2-hydroxyethyl)-oxamic acid; acetamide |
Increase Toxicity |
n.a. |
n.a. |
n.a. |
Probably increase its liver toxicity |
PMID: 26569070
|
Bacteroides fragilis |
Sorivudine |
Therapeutic Substance |
Investigational Drug |
Hydrolysis |
(E)-5-(2-bromovinyl) uracil |
Increase Toxicity |
n.a. |
n.a. |
Metabolites can inactivate a key liver enzyme |
Lead to lethal toxicity when co-administered with 5-fluorouracil |
PMID: 26569070; PMID: 27591027
|
Bacteroides thetaiotaomicron |
Sorivudine |
Therapeutic Substance |
Investigational Drug |
Hydrolysis |
(E)-5-(2-bromovinyl) uracil |
Increase Toxicity |
n.a. |
n.a. |
Metabolites can inactivate a key liver enzyme |
Lead to lethal toxicity when co-administered with 5-fluorouracil |
PMID: 26569070; PMID: 27591027
|
Bacteroides uniformis |
Sorivudine |
Therapeutic Substance |
Investigational Drug |
Hydrolysis |
(E)-5-(2-bromovinyl) uracil |
Increase Toxicity |
n.a. |
n.a. |
Metabolites can inactivate a key liver enzyme |
Lead to lethal toxicity when co-administered with 5-fluorouracil |
PMID: 26569070; PMID: 27591027
|
Bacteroides vulgatus |
Sorivudine |
Therapeutic Substance |
Investigational Drug |
Hydrolysis |
(E)-5-(2-bromovinyl) uracil |
Increase Toxicity |
n.a. |
n.a. |
Metabolites can inactivate a key liver enzyme |
Lead to lethal toxicity when co-administered with 5-fluorouracil |
PMID: 26569070; PMID: 27591027
|
Bacteroides eggerthii |
Sorivudine |
Therapeutic Substance |
Investigational Drug |
Hydrolysis |
(E)-5-(2-bromovinyl) uracil |
Increase Toxicity |
n.a. |
n.a. |
Metabolites can inactivate a key liver enzyme |
Lead to lethal toxicity when co-administered with 5-fluorouracil |
PMID: 26569070; PMID: 27591027
|
Unidentified gut microbes |
Mesalazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Microbial arylamine N-acetyltransferases |
Differences in gut microbial metabolism contribute to variations in drug efficacy |
PMID: 11344150; PMID: 26972811
|
Unidentified gut microbes |
Azo dyes |
Environmental Chemicals |
Industrial Chemicals and Pollutants |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Reduce azo bond |
n.a. |
PMID: 26972811; PMID: 14489780
|
Unidentified gut microbes |
Enrofloxacin |
Therapeutic Substance |
Investigational Drug |
n.a. |
n.a. |
n.a. |
Mouse |
Enrofloxacin-or vancomycin-treated |
Microbial fermentation of carbohydrates is disrupted |
Decrease concentrations of amino acids and SCFAs;increase oligosaccharide levels |
PMID: 18698804; PMID: 26972811
|
Unidentified gut microbes |
Vancomycin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
Mouse |
Enrofloxacin-or vancomycin-treated |
Microbial fermentation of carbohydrates is disrupted |
Decrease concentrations of amino acids and SCFAs;increase oligosaccharide levels |
PMID: 18698804; PMID: 26972811
|
Unidentified gut microbes |
Pentobarbital |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Animal model |
Germ-free,colonized |
n.a. |
Germ-free animals are more efficient at metabolizing drug |
PMID: 19742318; PMID: 26972811
|
Unidentified gut microbes |
Simvastatin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
Human |
n.a. |
n.a. |
Treatment is positively associated with the production by the microbiota(lithocholic acid, taurolithocholic acid and glycolithocholic acid) |
PMID: 22022402; PMID: 26972811
|
Unidentified gut microbes |
Oxaliplatin |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Production of reactive oxygen species |
Induces apoptosis |
PMID: 24264989; PMID: 26972811
|
Firmicutes |
Cyclophosphamide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Mouse |
n.a. |
Promote the translocation of bacteria into secondary lymphoid organs |
Limit tumour growth |
PMID: 24264990; PMID: 26972811
|
Eggerthella lenta |
Digoxin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
dihydrodigoxin |
Decrease Efficacy |
n.a. |
n.a. |
Cgr operon |
n.a. |
PMID: 6836275; PMID: 26972811
|
Unidentified gut microbes |
Heterocyclic amines |
Environmental Chemicals |
Unclassified Substance |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Β-glucuronidases |
Microbiota contribute to associations between the risk of CRC and the intake of heterocyclic amines |
PMID: 8055651; PMID: 26972811
|
Unidentified gut microbes |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
Increase Toxicity |
n.a. |
n.a. |
Microbial β-glucuronidase,liberate the sugar moiety from SN-38G |
Re-activate the drug causing increased toxicity(towards intestinal epithelial cells);exacerbate the diarrhoea |
PMID: 8891470; PMID: 26972811
|
Unidentified gut microbes |
7-ethyl-10-hydroxycamptothecin |
Therapeutic Substance |
Investigational Drug |
n.a. |
SN-38G; ;cyanuric acid |
Increase Toxicity |
Animal model |
Germ-free,colonized |
n.a. |
Metabolites are harmful to the host |
PMID: 26972811
|
Fusobacteria |
Acetaminophen |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
Increase Toxicity |
n.a. |
n.a. |
Microbial metabolite p-cresol competes with drug |
Impede the ability to detoxify acetaminophen,accumulate the toxic metabolite NAPQI |
PMID: 26972811
|
Clostridioides difficile |
Acetaminophen |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
Increase Toxicity |
n.a. |
n.a. |
Microbial metabolite p-cresol competes with drug |
Impede the ability to detoxify acetaminophen,accumulate the toxic metabolite NAPQI |
PMID: 26972811
|
Bacteroidetes |
Acetaminophen |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
Increase Toxicity |
n.a. |
n.a. |
Microbial metabolite p-cresol competes with drug |
Impede the ability to detoxify acetaminophen,accumulate the toxic metabolite NAPQI |
PMID: 26972811
|
Actinobacteria |
Acetaminophen |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
Increase Toxicity |
n.a. |
n.a. |
Microbial metabolite p-cresol competes with drug |
Impede the ability to detoxify acetaminophen,accumulate the toxic metabolite NAPQI |
PMID: 26972811
|
Bifidobacterium |
Anti-PD-L1 therapy |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Increase the efficacy of PD-1 |
PMID: 26972811
|
Staphylococcus |
Anti-TNF antibobies |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Therapy is accompanied by a substantial increase in the abundance of bacteria |
PMID: 26972811
|
Aspergillus nidulans |
Black tea |
Dietary Substance |
Drinks |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Increase the abundance of A. muciniphila |
PMID: 26972811
|
Proteobacteria |
Choline-containing compounds |
Environmental Chemicals |
Unclassified Substance |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Microbial glycyl radical enzymes |
Associate with the risk of cardiovascular disease |
PMID: 26972811
|
Firmicutes |
Choline-containing compounds |
Environmental Chemicals |
Unclassified Substance |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Microbial glycyl radical enzymes |
Associate with the risk of cardiovascular disease |
PMID: 26972811
|
Bacteroides fragilis |
CTLA-4 blockade |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Blockade immunotherapy |
PMID: 26972811
|
Bacteroides thetaiotaomicron |
CTLA-4 blockade |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Blockade immunotherapy |
PMID: 26972811
|
Enterococcus faecium |
Daidzin |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
equol |
n.a. |
n.a. |
n.a. |
Glycosidic cleavage and reduction |
n.a. |
PMID: 26972811
|
Bifidobacterium sp. |
Daidzin |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
equol |
n.a. |
n.a. |
n.a. |
Glycosidic cleavage and reduction |
n.a. |
PMID: 26972811
|
Lactobacillus mucosae |
Daidzin |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
equol |
n.a. |
n.a. |
n.a. |
Glycosidic cleavage and reduction |
n.a. |
PMID: 26972811
|
Eggerthella sp. |
Daidzin |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
equol |
n.a. |
n.a. |
n.a. |
Glycosidic cleavage and reduction |
n.a. |
PMID: 26972811
|
Unidentified gut microbes |
Dietary phosphatidylcholine |
Dietary Substance |
Dietary Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Bacteria provide a link for drugs |
PMID: 26972811
|
Gordonibacter |
Ellagic acid |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Metabolize ellagitannins |
PMID: 26972811
|
Aspergillus nidulans |
Grape-derived polyphenols |
Dietary Substance |
Dietary Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Increase the abundance of A. muciniphila |
PMID: 26972811
|
Unidentified gut microbes |
Heterocyclic amine 2-amino-3-methylimidazo[4,5-f]quinoline (IQ) |
Environmental Chemicals |
Unclassified Substance |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Reactivate the compound |
PMID: 26972811
|
Campylobacter |
Isoaminile |
Therapeutic Substance |
Approved Drug |
n.a. |
cyclohexylamine |
n.a. |
Animal model |
n.a. |
n.a. |
Exhibit toxicity |
PMID: 26972811
|
Escherichia |
Isoaminile |
Therapeutic Substance |
Approved Drug |
n.a. |
cyclohexylamine |
n.a. |
Animal model |
n.a. |
n.a. |
Exhibit toxicity |
PMID: 26972811
|
Enterococcus |
Isoaminile |
Therapeutic Substance |
Approved Drug |
n.a. |
cyclohexylamine |
n.a. |
Animal model |
n.a. |
n.a. |
Exhibit toxicity |
PMID: 26972811
|
Clostridium |
Isoaminile |
Therapeutic Substance |
Approved Drug |
n.a. |
cyclohexylamine |
n.a. |
Animal model |
n.a. |
n.a. |
Exhibit toxicity |
PMID: 26972811
|
Corynebacterium |
Isoaminile |
Therapeutic Substance |
Approved Drug |
n.a. |
cyclohexylamine |
n.a. |
Animal model |
n.a. |
n.a. |
Exhibit toxicity |
PMID: 26972811
|
Firmicutes |
Isoflavones |
Dietary Substance |
Dietary Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Metabolites bind to oestrogen receptors |
May elicit protective effects against breast cancer |
PMID: 26972811
|
Bacteroidetes |
Isoflavones |
Dietary Substance |
Dietary Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Metabolites bind to oestrogen receptors |
May elicit protective effects against breast cancer |
PMID: 26972811
|
Actinobacteria |
Isoflavones |
Dietary Substance |
Dietary Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Metabolites bind to oestrogen receptors |
May elicit protective effects against breast cancer |
PMID: 26972811
|
Firmicutes |
Lignans |
Herbal Substance; Dietary Substance |
Medicinal Herbal Compounds; Dietary Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Metabolites bind to oestrogen receptors |
May elicit protective effects against breast cancer |
PMID: 26972811
|
Bacteroidetes |
Lignans |
Herbal Substance; Dietary Substance |
Medicinal Herbal Compounds; Dietary Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Metabolites bind to oestrogen receptors |
May elicit protective effects against breast cancer |
PMID: 26972811
|
Actinobacteria |
Lignans |
Herbal Substance; Dietary Substance |
Medicinal Herbal Compounds; Dietary Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Metabolites bind to oestrogen receptors |
May elicit protective effects against breast cancer |
PMID: 26972811
|
Unidentified gut microbes |
Methotrexate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
Decrease Efficacy |
Animal model |
Germ-free,colonized |
Conversion into a downstream metabolite with reduced bioactivity |
n.a. |
PMID: 26972811
|
Unidentified gut microbes |
NSAIDs |
Therapeutic Substance |
Drug Class |
n.a. |
SN-38G; ;cyanuric acid |
Increase Toxicity |
Animal model |
Germ-free,colonized |
n.a. |
Metabolites are harmful to the host |
PMID: 26972811
|
Unidentified gut microbes |
Phenoxyethanol |
Therapeutic Substance |
Approved Drug |
n.a. |
SN-38G; ;cyanuric acid |
Increase Toxicity |
Animal model |
Germ-free,colonized |
n.a. |
Metabolites are harmful to the host |
PMID: 26972811
|
Raoultella terrigena |
Phenoxyethanol |
Therapeutic Substance |
Approved Drug |
n.a. |
cyanuric acid |
n.a. |
Animal model |
n.a. |
n.a. |
Lead to increased kidney damage |
PMID: 26972811
|
Raoultella terrigena |
Phenoxyethanol |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Metabolism by the bacteria |
Lead to kidney stones |
PMID: 26972811
|
Akkermansia muciniphila |
Polyphenols |
Herbal Substance; Dietary Substance |
Medicinal Herbal Compounds; Dietary Compounds |
n.a. |
n.a. |
n.a. |
Mouse |
Fed high-fat diets |
Couple with substantial sevenfold-to-tenfold blooms of drug |
Limit the risk of systemic inflammation |
PMID: 26972811
|
Clostridiales bacterium |
Saccharin |
Therapeutic Substance; Dietary Substance; Herbal Substance |
Investigational Drug; Dietary Compounds; Artificial Sweetener; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
Mouse |
Colonized with gut micro organisms from NAS-treated mice,or with faecal microorganisms |
n.a. |
Increase the abundance of bacteria |
PMID: 26972811
|
Unidentified gut microbes |
Secoisolariciresinol |
Therapeutic Substance |
Investigational Drug |
n.a. |
enterodiol,enterolactone |
n.a. |
n.a. |
n.a. |
n.a. |
Product the cancer-protective compounds |
PMID: 26972811
|
Unidentified gut microbes |
Simvastatin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
Increase Bioavailability |
n.a. |
n.a. |
Modulate the expression of host transporters,or directly compete with host transporters |
Contribute to the absorption of simvastatin |
PMID: 26972811
|
Unidentified gut microbes |
Sulfanilamide |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
Increase Efficacy |
Animal model |
Germ-free,colonized |
Conversion to bioactive form |
Contribute to therapeutic concentrations |
PMID: 26972811
|
Enterococcus faecalis |
Sulfasalazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Rat |
Antibiotic-treated or germ-free;convention |
n.a. |
Result in drug cleavage |
PMID: 26972811
|
Lactobacillus sp. |
Sulfasalazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Rat |
Antibiotic-treated or germ-free;convention |
n.a. |
Result in drug cleavage |
PMID: 26972811
|
Bacteroides sp. |
Sulfasalazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Rat |
Antibiotic-treated or germ-free;convention |
n.a. |
Result in drug cleavage |
PMID: 26972811
|
Unidentified gut microbes |
Sulfasalazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
Increase Efficacy |
Animal model |
Germ-free,colonized |
Conversion to bioactive form |
Contribute to therapeutic concentrations |
PMID: 26972811
|
Faecalibacterium prausnitzii |
Tacrolimus |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
Human |
Kidney transplant recipient |
n.a. |
The abundance of the gut bacterium has a positive correlation with an increase in tacrolimus dosing |
PMID: 26972811
|
Unidentified gut microbes |
TMAO |
Environmental Chemicals |
Human Metabolite |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Bacteria provide a link for drugs |
PMID: 26972811
|
Clostridiales bacterium |
Xylitol |
Therapeutic Substance; Herbal Substance |
|
n.a. |
n.a. |
n.a. |
Mouse |
Colonized with gut micro organisms from NAS-treated mice,or with faecal microorganisms |
n.a. |
Increase the abundance of bacteria |
PMID: 26972811
|
Bacteroidales |
Carboxymethylcellulose |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Mouse |
n.a. |
Decrease the abundance of Bacteroidales;increase the abundance of mucolytic bacteria |
The shifts in microbiota are accompanied by low-grade inflammation,increased gut permeability, increased weight and adiposity, and the development of metabolic syndrome |
PMID: 26972811
|
[Ruminococcus] gnavus |
Carboxymethylcellulose |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Mouse |
n.a. |
Decrease the abundance of Bacteroidales;increase the abundance of mucolytic bacteria |
The shifts in microbiota are accompanied by low-grade inflammation,increased gut permeability, increased weight and adiposity, and the development of metabolic syndrome |
PMID: 26972811
|
Bacteroidales |
Polysorbate 80 |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Mouse |
n.a. |
Decrease the abundance of Bacteroidales;increase the abundance of mucolytic bacteria |
The shifts in microbiota are accompanied by low-grade inflammation,increased gut permeability, increased weight and adiposity, and the development of metabolic syndrome |
PMID: 26972811
|
[Ruminococcus] gnavus |
Polysorbate 81 |
Environmental Chemicals |
Industrial Chemicals and Pollutants |
n.a. |
n.a. |
n.a. |
Mouse |
n.a. |
Decrease the abundance of Bacteroidales;increase the abundance of mucolytic bacteria |
The shifts in microbiota are accompanied by low-grade inflammation,increased gut permeability, increased weight and adiposity, and the development of metabolic syndrome |
PMID: 26972811
|
Escherichia coli |
Glucuronidated compound |
Environmental Chemicals |
Unclassified Substance |
n.a. |
n.a. |
n.a. |
Mouse |
Convention,germ-free |
Β-glucuronidases |
Reactivate the toxic compound and augment genotoxicity |
PMID: 26972811
|
Unidentified gut microbes |
Sulfanilamide |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
triamino benzene,sulfanilamide |
Increase Efficacy |
n.a. |
n.a. |
Reduce azo bond |
Activate drug |
PMID: 26972811
|
Enterococcus faecalis |
Secoisolariciresinol |
Therapeutic Substance |
Investigational Drug |
n.a. |
enterodiol and entero lactone |
Increase Efficacy |
Rat |
Germ-free,or germ-free colonized with a bacterial consortium |
Metabolism by bacteria |
Protective effects against breast cancer |
PMID: 26972811
|
Eubacterium limosum |
Secoisolariciresinol |
Therapeutic Substance |
Investigational Drug |
n.a. |
enterodiol and entero lactone |
Increase Efficacy |
Rat |
Germ-free,or germ-free colonized with a bacterial consortium |
Metabolism by bacteria |
Protective effects against breast cancer |
PMID: 26972811
|
[Clostridium] scindens |
Secoisolariciresinol |
Therapeutic Substance |
Investigational Drug |
n.a. |
enterodiol and entero lactone |
Increase Efficacy |
Rat |
Germ-free,or germ-free colonized with a bacterial consortium |
Metabolism by bacteria |
Protective effects against breast cancer |
PMID: 26972811
|
Blautia producta |
Secoisolariciresinol |
Therapeutic Substance |
Investigational Drug |
n.a. |
enterodiol and entero lactone |
Increase Efficacy |
Rat |
Germ-free,or germ-free colonized with a bacterial consortium |
Metabolism by bacteria |
Protective effects against breast cancer |
PMID: 26972811
|
Eggerthella lenta |
Secoisolariciresinol |
Therapeutic Substance |
Investigational Drug |
n.a. |
enterodiol and entero lactone |
Increase Efficacy |
Rat |
Germ-free,or germ-free colonized with a bacterial consortium |
Metabolism by bacteria |
Protective effects against breast cancer |
PMID: 26972811
|
Lactonifactor longoviformis |
Secoisolariciresinol |
Therapeutic Substance |
Investigational Drug |
n.a. |
enterodiol and entero lactone |
Increase Efficacy |
Rat |
Germ-free,or germ-free colonized with a bacterial consortium |
Metabolism by bacteria |
Protective effects against breast cancer |
PMID: 26972811
|
Unidentified gut microbes |
Diclofenac |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
Increase Toxicity |
n.a. |
n.a. |
Microbial β-glucuronidase |
Cause mitochondrial and endo plasmic reticulum stress, compromise mucosal integrity and promote inflammation |
PMID: 26972811
|
Unidentified gut microbes |
Indomethacin |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
Increase Toxicity |
n.a. |
n.a. |
Microbial β-glucuronidase |
Cause mitochondrial and endo plasmic reticulum stress, compromise mucosal integrity and promote inflammation |
PMID: 26972811
|
Unidentified gut microbes |
Ketoprofen |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
Increase Toxicity |
n.a. |
n.a. |
Microbial β-glucuronidase |
Cause mitochondrial and endo plasmic reticulum stress, compromise mucosal integrity and promote inflammation |
PMID: 26972811
|
Bacteroides |
Saccharin |
Therapeutic Substance; Dietary Substance; Herbal Substance |
Investigational Drug; Dietary Compounds; Artificial Sweetener; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
Mouse |
Colonized with gut micro organisms from NAS-treated mice,or with faecal microorganisms |
n.a. |
Increase the abundance of bacteria |
PMID: 26972811
|
Unidentified gut microbes |
Tempol |
Therapeutic Substance |
Investigational Drug |
n.a. |
n.a. |
n.a. |
Mouse |
n.a. |
n.a. |
Increase the abundance of Bacteroidetes;decrease the abundance of Firmicutes |
PMID: 26972811
|
Firmicutes |
Tempol |
Therapeutic Substance |
Investigational Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Reduce members of the genus Lactobacillus |
PMID: 26972811
|
Bacteroides |
Xylitol |
Therapeutic Substance; Herbal Substance |
|
n.a. |
n.a. |
n.a. |
Mouse |
Colonized with gut micro organisms from NAS-treated mice,or with faecal microorganisms |
n.a. |
Increase the abundance of bacteria |
PMID: 26972811
|
Lactobacillus |
Amoxicillin |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Decrease expression of genes involved in antimicrobial defence |
Nearly eradicated the lactobacilli |
PMID: 26972811
|
Clostridioides difficile |
Amoxicillin |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Piglet |
n.a. |
n.a. |
Promote colonization by opportunistic pathogens |
PMID: 26972811
|
Candida albicans |
Amoxicillin |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Piglet |
n.a. |
n.a. |
Promote colonization by opportunistic pathogens |
PMID: 26972811
|
Clostridioides difficile |
Antibiotic |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
Increase Toxicity |
n.a. |
n.a. |
n.a. |
Cause antibiotic-associated diarrhoea(AAD);pseudomembranous colitis(can cause death) |
PMID: 26972811
|
Candida albicans |
Cefoperazone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Total number of bacteria is reduced;overgrowth of C.albicans |
Allergic-airways diease develops after challenge with mould spores |
PMID: 26972811
|
Lactobacillus |
Cephalosporins |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Suppression of lactocilli and bifidobacterial;overgrowth of C.albicans |
Increase susceptibility to asthma |
PMID: 26972811
|
Bifidobacterium |
Cephalosporins |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Suppression of lactocilli and bifidobacterial;overgrowth of C.albicans |
Increase susceptibility to asthma |
PMID: 26972811
|
Candida albicans |
Cephalosporins |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Suppression of lactocilli and bifidobacterial;overgrowth of C.albicans |
Increase susceptibility to asthma |
PMID: 26972811
|
Lactobacillus |
Kanamycin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Total number of anaerobes is reduced |
Clinical scores for atopic dermatitis are higher |
PMID: 26972811
|
Bifidobacterium sp. |
Metronidazole |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
More bifidobacterium spp. |
PMID: 26972811
|
Gram-negative bacterium B1G-1A |
Metronidazole |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
Mouse |
n.a. |
Reduce expression of the gene encoding REG3γ |
n.a. |
PMID: 26972811
|
Gram-negative bacterium B1G-1A |
Neomycin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
Mouse |
n.a. |
Reduce expression of the gene encoding REG3γ |
n.a. |
PMID: 26972811
|
Salmonella enterica subsp. enterica serovar Typhimurium |
Streptomycin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
Mouse |
Streptomycin treated |
Butyrate contribute to the increased infiltration of neutrophils |
Result in an increased inflammatory state |
PMID: 26972811
|
Unidentified vaginal microbes |
Unspecified antibiotic |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Loss of vaginal lactobacilli;and overgrowth of C.albicans |
n.a. |
PMID: 26972811
|
Candida albicans |
Unspecified antibiotic |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Loss of vaginal lactobacilli;and overgrowth of C.albicans |
n.a. |
PMID: 26972811
|
Unidentified gut microbes |
Vancomycin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Gram-negatinve populations are depleted(not being restricted by vancomycin) |
PMID: 26972811
|
Gram-negative bacterium B1G-1A |
Vancomycin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
Mouse |
n.a. |
Reduce expression of the gene encoding REG3γ |
n.a. |
PMID: 26972811
|
Unidentified gut microbes |
Nizatidine |
Therapeutic Substance |
Approved Drug |
n.a. |
hydroxyiminonizatidine |
n.a. |
n.a. |
n.a. |
Cleavage on an N-oxide bond |
n.a. |
PMID: 27485182; PMID: 11955801
|
Unidentified gut microbes |
Nabumetone |
Therapeutic Substance |
Approved Drug |
n.a. |
4-(6-methoxy-2-naphthyl)-butan-2-ol (reduced nabumetone) |
Decrease Efficacy |
n.a. |
n.a. |
n.a. |
Cause lower absorbtion of nabumetone and lower its bioavailability;[drug interaction:erythromycin and tetracycline suppresses the reduction of digoxin] |
PMID: 23584048; PMID: 27485182
|
Unidentified gut microbes |
Lovastatin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
a phosphorylated derivative and active 2-hydroxy lovastatic acid |
n.a. |
Rat |
n.a. |
Hydrolyzed |
[drug interaction]:antibiotics decreases the bioavailability of the active metabolite |
PMID: 27485182; PMID: 24947972
|
Unidentified gut microbes |
Lovastatin related compounds |
Therapeutic Substance |
n.a. |
n.a. |
a phosphorylated derivative and active 2-hydroxy lovastatic acid |
n.a. |
Rat |
n.a. |
Hydrolyzed |
[drug interaction]:antibiotics decreases the bioavailability of the active metabolite |
PMID: 27485182; PMID: 24947972
|
Unidentified gut microbes |
Sulfinpyrazone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Human; Rabbit |
Healthy volunteers and ileostomy patients;/ |
Microbiota seems to be only site of sulfinpyrazone reduction(in man) |
n.a. |
PMID: 3630204; PMID: 27485182
|
Unidentified gut microbes |
Sulindac |
Therapeutic Substance |
Approved Drug |
n.a. |
sulindac sulfide |
n.a. |
Human; Rabbit |
n.a. |
n.a. |
n.a. |
PMID: 3630204; PMID: 27485182
|
Unidentified gut microbes |
Sulfasalazine |
Therapeutic Substance |
Approved Drug |
n.a. |
5-aminosalicylic acid (mesalazine)and sulfapyridine |
Decrease Toxicity |
n.a. |
n.a. |
Bacterial azoreductases |
Lead to side effect |
PMID: 27485182; PMID: 4147555
|
Unidentified gut microbes |
Chloramphenicol |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
p-aminophenyl-2-amin-1,3-propanediol |
Increase Toxicity |
human |
n.a. |
n.a. |
Produce toxic metabolite related to risk of marrow aplasia |
PMID: 27485182; PMID: 4165044
|
Unidentified anaerobic bacterium |
Metronidazole |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
N-(2-hydroxyethyl)-oxamic acid and acetamide |
n.a. |
Rat |
Conventional(CV),germ-free(GF) |
Reductive modification,disrupt the imidazole ring |
n.a. |
PMID: 27485182; PMID: 430360
|
Clostridium perfringens |
Metronidazole |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
N-(2-hydroxyethyl)-oxamic acid and acetamide |
n.a. |
Rat |
Conventional(CV),germ-free(GF) |
Reductive modification,disrupt the imidazole ring |
n.a. |
PMID: 27485182; PMID: 430360
|
Unidentified gut microbes |
Levodopa |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
m-tyramine and m-hydroxyphenylacetic acid |
n.a. |
Rat |
Conventional,in pathogen free |
Dehydroxylation of the catechol ring |
Form the metabolites |
PMID: 4723308; PMID: 27485182
|
Unidentified gut microbes |
Misonidazole |
Therapeutic Substance |
Investigational Drug |
n.a. |
amino derivative |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 6260109; PMID: 27485182
|
Unidentified gut microbes |
Balsalazide |
Therapeutic Substance |
Approved Drug |
n.a. |
5-aminosalicylic acid |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 27485182; PMID: 6345112
|
Unidentified gut microbes |
Clonazepam |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Rat |
Germ-free and ex-germ-free |
Nitro reduction |
n.a. |
PMID: 27485182; PMID: 6506755
|
Unidentified gut microbes |
Risperidone |
Therapeutic Substance |
Approved Drug |
n.a. |
dihydroxy-risperidone and hydroxyl-ke-to-risperidone |
n.a. |
Rat |
n.a. |
n.a. |
[drug interaction]:(in the liver)antibiotics decrease the bioavailability of risperidone. |
PMID: 27485182; PMID: 7512019
|
Unidentified gut microbes |
Omeprazole |
Therapeutic Substance |
Approved Drug |
n.a. |
sulfide metabolites |
n.a. |
n.a. |
n.a. |
Reductive metabolism |
n.a. |
PMID: 27485182; PMID: 7629748
|
Unidentified gut microbes |
Zonisamide |
Therapeutic Substance |
Approved Drug |
n.a. |
2-sulfamoylacetylphenol |
n.a. |
Mouse; Rat; Hamster; Rabbit; Guinea pig |
n.a. |
Reductive metabolism |
[drug interaction]:antibiotics inhibit the urinary and faecal excretion of metabolites |
PMID: 9231340; PMID: 27485182
|
Unidentified gut microbes |
Digoxin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
dihydrodigoxin and dihydrodigoxigenin |
Decrease Efficacy |
human |
n.a. |
Formation of inactive metabolites |
Have lower cardiac activity |
PMID: 27485182; PMID: 7266632
|
Unidentified gut microbes |
Mesalazine |
Therapeutic Substance |
Approved Drug |
n.a. |
N-acetyl-5-aminosalicylic acid |
n.a. |
Human; Rat; Guinea pig; Dog |
n.a. |
Acetylated by the gut microbiota |
n.a. |
PMID: 27485182
|
Unidentified gut microbes |
Sulfapyridine |
Therapeutic Substance |
Approved Drug |
n.a. |
N-acetyl-5-aminosalicylic acid |
n.a. |
Human; Rat; Guinea pig; Dog |
n.a. |
Acetylated by the gut microbiota |
n.a. |
PMID: 27485182
|
Clostridioides difficile |
Acetaminophen |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
p-cresol sulfate and phenylacetylglutamine |
Increase Toxicity |
n.a. |
n.a. |
O-sulfation; C-S cleavage of acetaminophen-3-cysteine |
Increased toxicity |
PMID: 27485182
|
Bacteroides |
Lactulose |
Therapeutic Substance |
Approved Drug |
n.a. |
fructose and galactose |
Increase Efficacy |
n.a. |
n.a. |
Hydrolysis of enzymes of the intestinal bacteria |
Lead to laxative effect of lactulose |
PMID: 27485182
|
Lactobacillus |
Lactulose |
Therapeutic Substance |
Approved Drug |
n.a. |
fructose and galactose |
Increase Efficacy |
n.a. |
n.a. |
Hydrolysis of enzymes of the intestinal bacteria |
Lead to laxative effect of lactulose |
PMID: 27485182
|
Escherichia coli |
Lactulose |
Therapeutic Substance |
Approved Drug |
n.a. |
fructose and galactose |
Increase Efficacy |
n.a. |
n.a. |
Hydrolysis of enzymes of the intestinal bacteria |
Lead to laxative effect of lactulose |
PMID: 27485182
|
Clostridium sp. |
Levamisole |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
levametabol-I,levametabol-II,and levametabol-III |
Increase Efficacy |
human |
n.a. |
Open thiazole ring |
Increased activity;[drug interaction]:antibiotics increase a stronger clinical effect of levamisole |
PMID: 27485182
|
Bacteroidetes |
Levamisole |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
levametabol-I,levametabol-II,and levametabol-III |
Increase Efficacy |
human |
n.a. |
Open thiazole ring |
Increased activity;[drug interaction]:antibiotics increase a stronger clinical effect of levamisole |
PMID: 27485182
|
Escherichia coli ATCC 25922 |
Nabumetone |
Therapeutic Substance |
Approved Drug |
n.a. |
a reduced pharmacologically inactive metabolite |
Decrease Efficacy |
n.a. |
n.a. |
n.a. |
Cause lower absorbtion and lower bioavailability of the drug |
PMID: 27485182
|
[Clostridium] leptum |
Nitrazepam |
Therapeutic Substance |
Approved Drug |
n.a. |
7-aminonitrazepam |
n.a. |
Mouse; Rat |
n.a. |
Nitro reduction |
Produce products with teratogenic effects |
PMID: 27485182
|
Bacteroides sp. |
Sorivudine |
Therapeutic Substance |
Investigational Drug |
n.a. |
(E)-5-(2-bromovinyl) uracil |
n.a. |
n.a. |
n.a. |
n.a. |
[drug interaction]:metabolites cause toxic level of anticancer drug 5-fluorouracil |
PMID: 27485182
|
Unidentified gut microbes |
Neoprontosil |
Therapeutic Substance |
Approved Drug |
n.a. |
sulfanilamide |
Increase Efficacy |
n.a. |
n.a. |
Reduction of the azo bond by azoreductases of the large intestinal microbiota |
Activate prodrug,have antibacterial effect;[drug interaction]:antbiotics suppress the conversion of prontosil |
PMID: 27485182
|
Unidentified gut microbes |
Sulfanilamide |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
sulfanilamide |
Increase Efficacy |
n.a. |
n.a. |
Reduction of the azo bond by azoreductases of the large intestinal microbiota |
Activate prodrug,have antibacterial effect;[drug interaction]:antbiotics suppress the conversion of prontosil |
PMID: 27485182
|
Unidentified gut microbes |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
SN-38 |
Increase Toxicity |
n.a. |
n.a. |
Β-glucuronidases |
Cause diarrhoea;[drug interaction]:(rat)ciprofloxacin and amoxapine can suppress diarrhoea |
PMID: 21051639; PMID: 28270698
|
Unidentified gut microbes |
CpG oligodeoxynucleotides |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
Mouse |
n.a. |
Bacteria regulate the immune response to chemotherapy(primes tumour-associated innate myeloid cells for inflammatory cytokine production) |
[drug interaction]:antibiotic or germ-free (sterile) status attenuates this response |
PMID: 24264989; PMID: 28270698
|
Unidentified gut microbes |
Cyclophosphamide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Mouse |
n.a. |
n.a. |
Cause commensal bacteria translocation into secondary lymphoid organs;reduce the abundance of lactobacilli and enterococci;[drug interaction]:long-term antibiotics reduce the capacity of cyclophosphamide |
PMID: 24264990; PMID: 28270698
|
Unidentified gut microbes |
Doxorubicin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
Mouse |
n.a. |
n.a. |
Cause commensal bacteria translocation into secondary lymphoid organs;reduce the abundance of lactobacilli and enterococci;[drug interaction]:long-term antibiotics reduce the capacity of cyclophosphamide |
PMID: 24264990; PMID: 28270698
|
Unidentified gut microbes |
Methotrexate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
Decrease Toxicity |
n.a. |
n.a. |
TLR2 signalling and drug transporter p-gp |
Bacteria regulate against chemotherapy-induced small bowel injury |
PMID: 25589072; PMID: 28270698
|
Unidentified gut microbes |
Ginsenosides |
Therapeutic Substance |
Investigational Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Metabolized via microbiota from compound K79 |
Metabolites have anti-proliferative effects in human colon cancer cells;[drug interaction]:co-treatment with 5-FU and its pro-drug intermediate 5’-deoxy-5-fluorouridine,potentiate the anticancer effects |
PMID: 25625815; PMID: 28270698
|
Unidentified gut microbes |
CTLA-4 blockade |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
Mouse |
Specific pathogen-free,germ-free(GF) |
n.a. |
MCA205 sarcoma progression is not controlled(in germ-free mice;or those treated with broad-spectrum antibiotics) |
PMID: 26541610; PMID: 28270698
|
Mycoplasma hyorhinis |
Floxuridine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Bacterium encode a thymidine phosphorylase |
Restrict the cytostatic activity of pyrimidine nucleoside analogue compounds |
PMID: 28270698
|
Mycoplasma hyorhinis |
Trifluridine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Bacterium encode a thymidine phosphorylase |
Restrict the cytostatic activity of pyrimidine nucleoside analogue compounds |
PMID: 28270698
|
Bifidobacterium sp. |
Anti-PD-L1 therapy |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
Mouse |
n.a. |
Exhibit the association with antitumour T-cell responses(through dendritic cell activation) |
Combination of microbiota and anti-PD-L1 improve tumour control,inducte tumour-specific T cells,increase T cells in the tumour microenvironment |
PMID: 28270698
|
Proteobacteria |
Carmustine, Etoposide, Cytarabine and melphalan combination |
Therapeutic Substance |
Drug Combination |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Reducte bacteria that limit inflammation,increase bacteria associated with colitis |
PMID: 28270698
|
Firmicutes |
Carmustine, Etoposide, Cytarabine and melphalan combination |
Therapeutic Substance |
Drug Combination |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Reducte bacteria that limit inflammation,increase bacteria associated with colitis |
PMID: 28270698
|
Actinobacteria |
Carmustine, Etoposide, Cytarabine and melphalan combination |
Therapeutic Substance |
Drug Combination |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Reducte bacteria that limit inflammation,increase bacteria associated with colitis |
PMID: 28270698
|
Ruminococcus |
CpG oligodeoxynucleotides |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 28270698
|
Alistipes |
CpG oligodeoxynucleotides |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 28270698
|
Burkholderiales |
CTLA-4 blockade |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
Mouse |
n.a. |
n.a. |
A cocktail of bacteria ameliorate CTLA-4-blockade-induced subclinical colitis and colon inflammatory scores in antibiotic-treated mice |
PMID: 28270698
|
Bacteroidales |
CTLA-4 blockade |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
Mouse |
n.a. |
n.a. |
A cocktail of bacteria ameliorate CTLA-4-blockade-induced subclinical colitis and colon inflammatory scores in antibiotic-treated mice |
PMID: 28270698
|
Segmented filamentous bacteria |
Cyclophosphamide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Gram-positive commensals mediate accumulation of TH17 and TH1-cell response |
PMID: 28270698
|
Lactobacillus |
Cyclophosphamide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Gram-positive commensals mediate accumulation of TH17 and TH1-cell response |
PMID: 28270698
|
Pseudomonas aeruginosa |
Cyclophosphamide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Mouse |
Fed a diet(high in protein, l-leucine, fish oil and specific oligosaccharides);an isoenergetic control die |
n.a. |
Reduce incidence and severity of Pseudomonas aeruginosa translocation |
PMID: 28270698
|
Enterococcus hirae |
Cyclophosphamide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Mouse |
Inoculated with MCA205 tumours;microbiota-depleted |
As an orchestrator of cyclophosphamide effects |
n.a. |
PMID: 28270698
|
Barnesiella intestinihominis |
Cyclophosphamide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Mouse |
Inoculated with MCA205 tumours;microbiota-depleted |
As an orchestrator of cyclophosphamide effects |
n.a. |
PMID: 28270698
|
Enterococcus hirae |
Cyclophosphamide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Commensal bacteria cross the intestinal barrier to enter secondary lymphoid organs |
PMID: 28270698
|
Lactobacillus murinus |
Cyclophosphamide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Commensal bacteria cross the intestinal barrier to enter secondary lymphoid organs |
PMID: 28270698
|
Lactobacillus johnsonii |
Cyclophosphamide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Commensal bacteria cross the intestinal barrier to enter secondary lymphoid organs |
PMID: 28270698
|
Enterococcus hirae |
Doxorubicin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Commensal bacteria cross the intestinal barrier to enter secondary lymphoid organs |
PMID: 28270698
|
Lactobacillus murinus |
Doxorubicin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Commensal bacteria cross the intestinal barrier to enter secondary lymphoid organs |
PMID: 28270698
|
Lactobacillus johnsonii |
Doxorubicin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Commensal bacteria cross the intestinal barrier to enter secondary lymphoid organs |
PMID: 28270698
|
Unidentified gut microbes |
Ellagic acid |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
urolithins |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 28270698
|
Mycoplasma |
Gemcitabine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
Decrease Efficacy |
n.a. |
n.a. |
Pyrimidine nucleoside phosphorylase and cytidine deaminase enzyme |
Have deleterious effects on its therapeutic efficacy |
PMID: 28270698
|
Bacteroidetes |
Ipilimumab |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Bacterially mediated B vitamin production and polyamine transport deficiencies |
Bacteria is associated with increased risk of CTLA‑4 blockade‑induced colitis |
PMID: 28270698
|
Enterobacteriaceae |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Rat |
n.a. |
Increase abundance of bacteria |
Cause diarrhoea; |
PMID: 28270698
|
Streptococcus thermophilus |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Rat |
n.a. |
n.a. |
Reduce diarrhoea and weight loss,increase intestinal crypt proliferation,inhibit apoptosis |
PMID: 28270698
|
Clostridioides difficile |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Rat |
n.a. |
Increase abundance of bacteria |
Cause diarrhoea; |
PMID: 28270698
|
Lactobacillus acidophilus |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Rat |
n.a. |
n.a. |
Reduce diarrhoea and weight loss,increase intestinal crypt proliferation,inhibit apoptosis |
PMID: 28270698
|
Lactobacillus plantarum |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Rat |
n.a. |
n.a. |
Reduce diarrhoea and weight loss,increase intestinal crypt proliferation,inhibit apoptosis |
PMID: 28270698
|
Lactobacillus paracasei |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Rat |
n.a. |
n.a. |
Reduce diarrhoea and weight loss,increase intestinal crypt proliferation,inhibit apoptosis |
PMID: 28270698
|
Bifidobacterium breve |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Rat |
n.a. |
n.a. |
Reduce diarrhoea and weight loss,increase intestinal crypt proliferation,inhibit apoptosis |
PMID: 28270698
|
Bifidobacterium longum |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Rat |
n.a. |
n.a. |
Reduce diarrhoea and weight loss,increase intestinal crypt proliferation,inhibit apoptosis |
PMID: 28270698
|
Lactobacillus delbrueckii subsp. bulgaricus |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Rat |
n.a. |
n.a. |
Reduce diarrhoea and weight loss,increase intestinal crypt proliferation,inhibit apoptosis |
PMID: 28270698
|
Bifidobacterium longum subsp. infantis |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Rat |
n.a. |
n.a. |
Reduce diarrhoea and weight loss,increase intestinal crypt proliferation,inhibit apoptosis |
PMID: 28270698
|
Unidentified gut microbes |
Methotrexate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Reduce diversity and shift in relative abundance associated with chemotherapy-induced diarrhoea |
PMID: 28270698
|
Unidentified gut microbes |
Methotrexate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Rat |
n.a. |
n.a. |
Reduce microbial abundance(decrease anaerobes and streptococci,relative increase of Bacteroides);change in microbiota is associated with diarrhoea |
PMID: 28270698
|
Bacteroides |
Methotrexate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Reduce diversity and shift in relative abundance associated with chemotherapy-induced diarrhoea |
PMID: 28270698
|
Bacteroides |
Methotrexate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Rat |
n.a. |
n.a. |
Reduce microbial abundance(decrease anaerobes and streptococci,relative increase of Bacteroides);change in microbiota is associated with diarrhoea |
PMID: 28270698
|
Streptococcus |
Methotrexate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Reduce diversity and shift in relative abundance associated with chemotherapy-induced diarrhoea |
PMID: 28270698
|
Streptococcus |
Methotrexate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Rat |
n.a. |
n.a. |
Reduce microbial abundance(decrease anaerobes and streptococci,relative increase of Bacteroides);change in microbiota is associated with diarrhoea |
PMID: 28270698
|
Bacteroidetes |
Polysaccharides (after cyclophosphamide administration) |
Dietary Substance |
Dietary Compounds |
n.a. |
n.a. |
n.a. |
Mouse |
n.a. |
n.a. |
Resulte in the enrichment of bifidobacteria and a reduction in the levels of Bacteroidetes;might protect against the adverse effects of chemotherapy |
PMID: 28270698
|
Bifidobacterium |
Polysaccharides (after cyclophosphamide administration) |
Dietary Substance |
Dietary Compounds |
n.a. |
n.a. |
n.a. |
Mouse |
n.a. |
n.a. |
Resulte in the enrichment of bifidobacteria and a reduction in the levels of Bacteroidetes;might protect against the adverse effects of chemotherapy |
PMID: 28270698
|
Bacteroides fragilis |
Sorivudine |
Therapeutic Substance |
Investigational Drug |
n.a. |
(E)-5-(2-bromovinyl) uracil (BVU) |
n.a. |
n.a. |
n.a. |
Gut bacterial phosphorolytic enzyme |
[drug interaction]:combination with 5-FU can increase in systemic concentrations of 5-FU and is associated with the death of patients |
PMID: 28270698
|
Bacteroides thetaiotaomicron |
Sorivudine |
Therapeutic Substance |
Investigational Drug |
n.a. |
(E)-5-(2-bromovinyl) uracil (BVU) |
n.a. |
n.a. |
n.a. |
Gut bacterial phosphorolytic enzyme |
[drug interaction]:combination with 5-FU can increase in systemic concentrations of 5-FU and is associated with the death of patients |
PMID: 28270698
|
Bacteroides uniformis |
Sorivudine |
Therapeutic Substance |
Investigational Drug |
n.a. |
(E)-5-(2-bromovinyl) uracil (BVU) |
n.a. |
n.a. |
n.a. |
Gut bacterial phosphorolytic enzyme |
[drug interaction]:combination with 5-FU can increase in systemic concentrations of 5-FU and is associated with the death of patients |
PMID: 28270698
|
Bacteroides vulgatus |
Sorivudine |
Therapeutic Substance |
Investigational Drug |
n.a. |
(E)-5-(2-bromovinyl) uracil (BVU) |
n.a. |
n.a. |
n.a. |
Gut bacterial phosphorolytic enzyme |
[drug interaction]:combination with 5-FU can increase in systemic concentrations of 5-FU and is associated with the death of patients |
PMID: 28270698
|
Bacteroides eggerthii |
Sorivudine |
Therapeutic Substance |
Investigational Drug |
n.a. |
(E)-5-(2-bromovinyl) uracil (BVU) |
n.a. |
n.a. |
n.a. |
Gut bacterial phosphorolytic enzyme |
[drug interaction]:combination with 5-FU can increase in systemic concentrations of 5-FU and is associated with the death of patients |
PMID: 28270698
|
Unidentified gut microbes |
Neoprontosil |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Microbiota-driven drug metabolism |
Affect drug disposition and toxicity |
PMID: 28270698
|
Unidentified gut microbes |
Sulfanilamide |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Microbiota-driven drug metabolism |
Affect drug disposition and toxicity |
PMID: 28270698
|
Bacteroides thetaiotaomicron |
Brivudine |
Therapeutic Substance |
Approved Drug |
n.a. |
bromovinyluracil (BVU) |
Increase Toxicity |
Mouse |
Conventional(CV),germ-free(GF) |
Microbial enzymes |
Conversion to hepatotoxic BVU;(GF)reduce systemic BVU exposure |
PMID: 30733391
|
Bacteroides ovatus |
Brivudine |
Therapeutic Substance |
Approved Drug |
n.a. |
bromovinyluracil (BVU) |
Increase Toxicity |
n.a. |
n.a. |
n.a. |
Conversion to hepatotoxic BVU;(GF)reduce systemic BVU exposure |
PMID: 30733391
|
Unidentified gut microbes |
Clonazepam |
Therapeutic Substance |
Approved Drug |
n.a. |
aminoclonazepam (NH2-CLZ),aminohydroxyclonazepam (NH2OH-CLZ) |
Increase Toxicity |
Mouse |
Conventional(CV),germ-free(GF) |
Contribute to the reductive metabolism of CLZ |
Lead to toxicity |
PMID: 30733391
|
Bacteroides thetaiotaomicron |
Sorivudine |
Therapeutic Substance |
Investigational Drug |
n.a. |
bromovinyluracil (BVU) |
Increase Toxicity |
Mouse |
Conventional(CV),germ-free(GF) |
Microbial enzymes |
Metabolized by members of this genus |
PMID: 30733391
|
Bacteroides ovatus |
Sorivudine |
Therapeutic Substance |
Investigational Drug |
n.a. |
bromovinyluracil (BVU) |
Increase Toxicity |
n.a. |
n.a. |
n.a. |
Metabolized by members of this genus |
PMID: 30733391
|
Unidentified gut microbes |
Lovastatin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
2-hydroxy lovastatic acid,2-hydroxy simvastatin acid |
Increase Efficacy |
Rat |
n.a. |
n.a. |
Product an active form;drug interaction:antibiotics suppresses the pharmacologic effects |
PMID: 9728898; PMID: 24947972; PMID: 25926432; PMID: 25571290
|
Unidentified gut microbes |
Simvastatin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
2-hydroxy lovastatic acid,2-hydroxy simvastatin acid |
Increase Efficacy |
Rat |
n.a. |
n.a. |
Product an active form;drug interaction:antibiotics suppresses the pharmacologic effects |
PMID: 9728898; PMID: 24947972; PMID: 25926432; PMID: 25571290
|
Clostridium perfringens |
Metronidazole |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
N-(2-hydroxyethyl)-oxamic acid and acetamide |
n.a. |
Rat |
n.a. |
Reduced metabolites |
n.a. |
PMID: 231450; PMID: 430360; PMID: 25926432
|
Streptococcus pyogenes |
Sulfanilamide |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
sulfanilamide |
Increase Efficacy |
Mouse |
A murine model of Streptococcus pyogenes systemic infection |
The gut microbiota transformed drug by azoreductases |
Exhibit potent antibacterial activity;drug interaction:antibiotics suppresses the conversion |
PMID: 4405598; Peppercorn and Goldman,1976; PMID: 25926432
|
Unidentified gut microbes |
Daidzein |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
calycosin |
n.a. |
n.a. |
n.a. |
Aromatic hydroxylase and O-methyltransferase |
Drug interaction:antibiotics suppresses the transformation |
PMID: 9657051; PMID: 25926432; PMID: 9781846
|
Unidentified gut microbes |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
SN-38 |
Increase Toxicity |
n.a. |
n.a. |
The b-glucuronidases of the gut microbiota |
Causes diarrhea;drug interaction:coadministration of the poorly absorbed aminoglycoside antibiotic neomycin could be advantageous for diarrhea |
PMID: 25926432; PMID: 11350876
|
Unidentified gut microbes |
Sulindac sulfide |
Environmental Chemicals |
Active Metabolite of Prodrug |
n.a. |
n.a. |
n.a. |
Human |
Healthy,ileostomy |
n.a. |
Drug interaction:metronidazole decreases the formation of sulfides of sulindac ex vivo |
PMID: 3630204; PMID: 25926432
|
Unidentified gut microbes |
Neoprontosil |
Therapeutic Substance |
Approved Drug |
n.a. |
sulfanilamide |
Increase Efficacy |
Rat |
n.a. |
n.a. |
Product the pharmacologically active metabolite;drug interaction:antibiotics reduced the amount of sulfanilamide excreted in the urine after oral administration |
PMID: 5173017; PMID: 25926432
|
Unidentified gut microbes |
Misonidazole |
Therapeutic Substance |
Investigational Drug |
n.a. |
1-(2-aminoimidazol-1-yl)-3-methoxypropan-2-ol |
Increase Toxicity |
Rat |
Convention,germ-free |
n.a. |
Drug interaction:antibiotic inhibits misonidazole transformation and toxicity |
PMID: 6260109; PMID: 25926432
|
Unidentified gut microbes |
Clonazepam |
Therapeutic Substance |
Approved Drug |
n.a. |
7-aminoclonazepam |
n.a. |
Rat |
Germ-free and ex–germ-free |
The reductive metabolism |
Drug interaction:antibiotic suppresses the reduction |
PMID: 6506755; PMID: 25926432
|
Unidentified gut microbes |
Loperamide oxide |
Therapeutic Substance |
Investigational Drug |
n.a. |
loperamide |
n.a. |
Rat; Dog |
n.a. |
Microbiota is involved in reduction |
Drug interaction:absorption of orally delivered loperamide oxide is lower when administered with cotrimoxazole |
PMID: 25926432; PMID: 8838438
|
Unidentified gut microbes |
Daidzin |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
daidzein,calycosin |
Increase Efficacy |
n.a. |
n.a. |
C-glucosidases and O-glucosidases |
Drug interaction:Antibiotic inhibits the metabolism of isoflavone glycosides |
PMID: 9657051; PMID: 25926432
|
Unidentified gut microbes |
Puerarin |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
daidzein,calycosin |
Increase Efficacy |
n.a. |
n.a. |
C-glucosidases and O-glucosidases |
Drug interaction:Antibiotic inhibits the metabolism of isoflavone glycosides |
PMID: 9657051; PMID: 25926432
|
Unidentified gut microbes |
Fenfluramine |
Therapeutic Substance |
Approved Drug |
n.a. |
phenolic acids |
n.a. |
Human; Mouse |
n.a. |
Deglycosylating enzymes of bacteria |
Metabolites might exhibit aspirin-like pharmacologic effects;drug interaction:antibiotics reduces metabolites excreted into the urine of rats |
PMID: 25926432; PMID: 9875509
|
Unidentified gut microbes |
Hesperidin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
phenolic acids |
n.a. |
Human; Mouse |
n.a. |
Deglycosylating enzymes of bacteria |
Metabolites might exhibit aspirin-like pharmacologic effects;drug interaction:antibiotics reduces metabolites excreted into the urine of rats |
PMID: 25926432; PMID: 9875509
|
Unidentified gut microbes |
Naringenin |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
phenolic acids |
n.a. |
Human; Mouse |
n.a. |
Deglycosylating enzymes of bacteria |
Metabolites might exhibit aspirin-like pharmacologic effects;drug interaction:antibiotics reduces metabolites excreted into the urine of rats |
PMID: 25926432; PMID: 9875509
|
Unidentified gut microbes |
Rutin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
phenolic acids |
n.a. |
Human; Mouse |
n.a. |
Deglycosylating enzymes of bacteria |
Metabolites might exhibit aspirin-like pharmacologic effects;drug interaction:antibiotics reduces metabolites excreted into the urine of rats |
PMID: 25926432; PMID: 9875509
|
Unidentified gut microbes |
Scutellaria baicalensis root |
Therapeutic Substance |
Investigational Drug |
n.a. |
phenolic acids |
n.a. |
Human; Mouse |
n.a. |
Deglycosylating enzymes of bacteria |
Metabolites might exhibit aspirin-like pharmacologic effects;drug interaction:antibiotics reduces metabolites excreted into the urine of rats |
PMID: 25926432; PMID: 9875509
|
Unidentified gut microbes |
Wognoside |
Herbal Substance |
Medicinal Herbal Compounds |
n.a. |
phenolic acids |
n.a. |
Human; Mouse |
n.a. |
Deglycosylating enzymes of bacteria |
Metabolites might exhibit aspirin-like pharmacologic effects;drug interaction:antibiotics reduces metabolites excreted into the urine of rats |
PMID: 25926432; PMID: 9875509
|
Unidentified gut microbes |
Digoxin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
dihydrodigoxin,dihydrodigoxigenin |
Decrease Efficacy |
Human |
n.a. |
n.a. |
Convert to the inactive metabolites;attenuates the drug’s effects;drug interaction:antibiotics(erythromycin and tetracycline)blocks the reduction of digoxin |
PMID: 25926432; PMID:7266632
|
Unidentified gut microbes |
Sulindac |
Therapeutic Substance |
Approved Drug |
n.a. |
sulindac sulfide |
n.a. |
Rabbit |
n.a. |
n.a. |
n.a. |
PMID: 25926432
|
Unidentified gut microbes |
Chloramphenicol |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
Decrease Efficacy |
n.a. |
n.a. |
Transform drugs and phytochemicals into bioinactive metabolites |
Affect the pharmacokinetics |
PMID: 25926432
|
Lactococcus garvieae |
Daidzein |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
5-hydroxy-equol |
n.a. |
Human; Animal models |
n.a. |
n.a. |
n.a. |
PMID: 25926432
|
Adlercreutzia equolifaciens |
Daidzein |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
5-hydroxy-equol |
n.a. |
Human; Animal models |
n.a. |
n.a. |
n.a. |
PMID: 25926432
|
Slackia equolifaciens |
Daidzein |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
5-hydroxy-equol |
n.a. |
Human; Animal models |
n.a. |
n.a. |
n.a. |
PMID: 25926432
|
Slackia isoflavoniconvertens |
Daidzein |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
5-hydroxy-equol |
n.a. |
Human; Animal models |
n.a. |
n.a. |
n.a. |
PMID: 25926432
|
Lactococcus garvieae |
Genistein |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
5-hydroxy-equol |
n.a. |
Human; Animal models |
n.a. |
n.a. |
n.a. |
PMID: 25926432
|
Adlercreutzia equolifaciens |
Genistein |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
5-hydroxy-equol |
n.a. |
Human; Animal models |
n.a. |
n.a. |
n.a. |
PMID: 25926432
|
Slackia equolifaciens |
Genistein |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
5-hydroxy-equol |
n.a. |
Human; Animal models |
n.a. |
n.a. |
n.a. |
PMID: 25926432
|
Slackia isoflavoniconvertens |
Genistein |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
5-hydroxy-equol |
n.a. |
Human; Animal models |
n.a. |
n.a. |
n.a. |
PMID: 25926432
|
Ruminococcus sp. |
Ginsenoside Rb1 |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
20-O-20-O-b-D-glucopyranosyl-20(S)-protopanaxadiol (compound K) |
Increase Efficacy |
n.a. |
n.a. |
n.a. |
Drug interaction:antibiotics inhibits the metabolism |
PMID: 25926432
|
Oscillibacter sp. |
Ginsenoside Rb1 |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
20-O-20-O-b-D-glucopyranosyl-20(S)-protopanaxadiol (compound K) |
Increase Efficacy |
n.a. |
n.a. |
n.a. |
Drug interaction:antibiotics inhibits the metabolism |
PMID: 25926432
|
Sutterella sp. |
Ginsenoside Rb1 |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
20-O-20-O-b-D-glucopyranosyl-20(S)-protopanaxadiol (compound K) |
Increase Efficacy |
n.a. |
n.a. |
n.a. |
Drug interaction:antibiotics inhibits the metabolism |
PMID: 25926432
|
Holdemania sp. |
Ginsenoside Rb1 |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
20-O-20-O-b-D-glucopyranosyl-20(S)-protopanaxadiol (compound K) |
Increase Efficacy |
n.a. |
n.a. |
n.a. |
Drug interaction:antibiotics inhibits the metabolism |
PMID: 25926432
|
Unidentified gut microbes |
Ginsenoside Rb1 |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
Increase Efficacy |
n.a. |
n.a. |
Transform drugs and phytochemicals into bioactive metabolites |
Affect the pharmacokinetics |
PMID: 25926432
|
Bacteroides |
Lactulose |
Therapeutic Substance |
Approved Drug |
n.a. |
fructose,galactose |
n.a. |
n.a. |
n.a. |
n.a. |
Drug interaction:combination treatment with neomycin and lactulose reduces the blood ammonia concentration in pigs |
PMID: 25926432
|
Lactobacillus |
Lactulose |
Therapeutic Substance |
Approved Drug |
n.a. |
fructose,galactose |
n.a. |
n.a. |
n.a. |
n.a. |
Drug interaction:combination treatment with neomycin and lactulose reduces the blood ammonia concentration in pigs |
PMID: 25926432
|
Escherichia coli |
Lactulose |
Therapeutic Substance |
Approved Drug |
n.a. |
fructose,galactose |
n.a. |
n.a. |
n.a. |
n.a. |
Drug interaction:combination treatment with neomycin and lactulose reduces the blood ammonia concentration in pigs |
PMID: 25926432
|
Clostridium sp. |
Levamisole |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
levametabol-I, levametabol-II, and levametabol-III |
n.a. |
n.a. |
n.a. |
n.a. |
Drug interaction: Combined therapy with tetracycline and levamisole has a stronger biologic effect |
PMID: 25926432
|
Bacteroides spp. |
Levamisole |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
levametabol-I, levametabol-II, and levametabol-III |
n.a. |
n.a. |
n.a. |
n.a. |
Drug interaction: Combined therapy with tetracycline and levamisole has a stronger biologic effect |
PMID: 25926432
|
Unidentified gut microbes |
Lovastatin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
Increase Efficacy |
n.a. |
n.a. |
Transform drugs and phytochemicals into bioactive metabolites |
Affect the pharmacokinetics |
PMID: 25926432
|
Unidentified gut microbes |
Metronidazole |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
Decrease Efficacy |
n.a. |
n.a. |
Transform drugs and phytochemicals into bioinactive metabolites |
Affect the pharmacokinetics |
PMID: 25926432
|
[Eubacterium] rectale |
Picosulfuric acid |
Therapeutic Substance |
Approved Drug |
n.a. |
free diphenol[4,49-(pyridin-2-ylmethanediyl)diphenol] |
Increase Efficacy |
n.a. |
n.a. |
Arylsulfate sulfotransferase of bacteria |
Have a laxative effect;drug interaction:antibiotics inhibits the transformation |
PMID: 25926432
|
Unidentified gut microbes |
Ranitidine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
Decrease Efficacy |
n.a. |
n.a. |
Transform drugs and phytochemicals into bioinactive metabolites |
Affect the pharmacokinetics |
PMID: 25926432
|
Unidentified gut microbes |
Sulfasalazine |
Therapeutic Substance |
Approved Drug |
n.a. |
5-aminosalicylic acid |
Increase Efficacy |
n.a. |
n.a. |
Azoreductases produced by metabolize |
Induces anti-inflammatory effects |
PMID: 25926432
|
Unidentified gut microbes |
Epicatechin |
Therapeutic Substance |
Investigational Drug |
n.a. |
phenolic acids |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 25926432
|
Unidentified gut microbes |
Anthocyanidins |
Herbal Substance |
Plant Compounds |
n.a. |
phenolic acids |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 25926432
|
Unidentified gut microbes |
Balsalazide |
Therapeutic Substance |
Approved Drug |
n.a. |
5-aminosalicylic acid |
n.a. |
Human |
n.a. |
n.a. |
Drug interaction:antibiotic suppresses the metabolism,limit its effectiveness |
PMID: 25926432
|
Unidentified gut microbes |
Cianidanol |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
phenolic acids |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 25926432
|
Unidentified gut microbes |
Flucytosine |
Therapeutic Substance |
Approved Drug |
n.a. |
5-fluorouracil |
n.a. |
n.a. |
n.a. |
n.a. |
Drug interaction:antimicrobial agents may reduce the antifungal effect of flucytosine |
PMID: 25926432
|
Unidentified gut microbes |
Glycyrrhizic acid |
Therapeutic Substance |
Approved Drug |
n.a. |
18b-glycyrrhetic acid |
n.a. |
Rat |
Germ-free |
n.a. |
Drug interaction:antibiotics(amoxicillin and metronidazole)suppresses the conversion |
PMID: 25926432
|
Unidentified gut microbes |
Hesperidin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
hesperetin |
n.a. |
Rat |
n.a. |
n.a. |
Suppress gut bacterial glycosidase activities;drug interaction:Antibiotic inhibits the metabolism |
PMID: 25926432
|
Unidentified gut microbes |
Levodopa |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
tyramine,m-hydroxyphenylacetic acid |
n.a. |
n.a. |
n.a. |
n.a. |
Drug interaction:antibiotics(vancomycin)inhibits the dehydroxylation of bile acid by the gut microbiota |
PMID: 25926432
|
Unidentified gut microbes |
Nitrazepam |
Therapeutic Substance |
Approved Drug |
n.a. |
7-amino-nitrazepam |
Increase Toxicity |
Rat |
n.a. |
Transform drugs and phytochemicals into toxic metabolites |
Affect the pharmacokinetics,product an active teratogenic substance;drug interaction: antibiotic reduced nitrazepam-induced teratogenicity |
PMID: 25926432
|
Unidentified gut microbes |
Nizatidine |
Therapeutic Substance |
Approved Drug |
n.a. |
hydroxyiminonizatidine |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 25926432
|
Unidentified gut microbes |
Ranitidine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
hydroxyiminoranitidine |
n.a. |
n.a. |
n.a. |
n.a. |
Drug interaction:antibiotics(rifampicin)decreases the absorption of ranitidine |
PMID: 25926432
|
Unidentified gut microbes |
Risperidone |
Therapeutic Substance |
Approved Drug |
n.a. |
dihydroxy-risperidone,hydroxy-keto-risperidone |
n.a. |
Rat |
n.a. |
Scission of isoxazole |
Drug interaction:Antibiotics(rifampin)inhibit the bioavailability of risperidone in the liver |
PMID: 25926432
|
Unidentified gut microbes |
Scutellaria baicalensis root |
Therapeutic Substance |
Investigational Drug |
n.a. |
oroxylin A |
n.a. |
n.a. |
n.a. |
Aromatic hydroxylase and O-methyltransferase |
n.a. |
PMID: 25926432
|
Unidentified gut microbes |
Sennosides |
Therapeutic Substance |
Investigational Drug |
n.a. |
rheinanthrone |
Increase Efficacy |
n.a. |
n.a. |
Reductase(s) and 3- b-D-glucosidase(s) |
Product a purgative compound;drug interaction:antibiotics(chloramphenicol, streptomycin, and rifampicin)inhibits the biotransformation |
PMID: 25926432
|
Unidentified gut microbes |
Sulfinpyrazone |
Therapeutic Substance |
Approved Drug |
n.a. |
sulfinpyrazone sulfide |
n.a. |
Rabbit |
n.a. |
n.a. |
Drug interaction:Metronidazole decreases the extent of sulfinpyrazone reduction in rabbits in vivo |
PMID: 25926432
|
Unidentified gut microbes |
Zonisamide |
Therapeutic Substance |
Approved Drug |
n.a. |
2-sulfamoyacetylphenol |
n.a. |
n.a. |
n.a. |
Through the reduction |
n.a. |
PMID: 25926432
|
Unidentified gut microbes |
Hydrazine |
Environmental Chemicals |
Industrial Chemicals; Medicinal chemicals |
n.a. |
n.a. |
Decrease Toxicity |
Rat |
n.a. |
DszA/NtaA-like oxygenase |
n.a. |
PMID: 19396371; PMID: 26261284
|
Unidentified anaerobic bacterium |
Fostamatinib |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
O-demethylation and dihydroxylation by bacteria |
n.a. |
PMID: 26261284; PMID: 20371637
|
Unidentified gut microbes |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
Increase Toxicity |
n.a. |
n.a. |
Reactivated by bacterially expressed b-glucuronidase |
Result in diarrhea |
PMID: 26261284; PMID: 21051639
|
Unidentified gut microbes |
BILR355 |
Therapeutic Substance |
Investigational Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Bacterially mediated N-oxide reduction |
Drug interaction:(with ritonavir)bacterial mediated reactions predominate |
PMID: 26261284; PMID: 22393121
|
Unidentified gut microbes |
2-chloro-5-nitro-N-phenylbenzamide |
Therapeutic Substance |
Investigational Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Bacterial nitroreductases |
Alter its mutagenicity |
PMID: 26261284; PMID: 22450444
|
Unidentified gut microbes |
Antiobiotics |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Drug interaction:antibiotics effect the functional activity of bacteria |
PMID: 26261284; PMID: 23332745
|
Unidentified gut microbes |
Digoxin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Drug interaction:antibiotics effect the functional activity of bacteria |
PMID: 26261284; PMID: 23332745
|
Unidentified gut microbes |
Phenacetin |
Therapeutic Substance |
Approved Drug (Withdrawn) |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Drug interaction:antibiotics effect the functional activity of bacteria |
PMID: 26261284; PMID: 23332745
|
Unidentified gut microbes |
Sulfasalazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Drug interaction:antibiotics effect the functional activity of bacteria |
PMID: 26261284; PMID: 23332745
|
Sulfite-reducing bacterium LF11mE1 |
Saturated fats |
Dietary Substance |
Dietary Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Excess consumption of fat leads to an increase in the growth of bacteria |
Increase the formation of proinflammatory and genotoxic secondary bile acids(deoxycholate) |
PMID: 26261284; PMID: 24355793
|
Clostridioides difficile |
Saturated fats |
Dietary Substance |
Dietary Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Excess consumption of fat leads to an increase in the growth of bacteria |
Increase the formation of proinflammatory and genotoxic secondary bile acids(deoxycholate) |
PMID: 26261284; PMID: 24355793
|
Unidentified gut microbes |
Arsenic |
Environmental Chemicals |
Toxic Agents |
n.a. |
n.a. |
n.a. |
Mouse |
n.a. |
n.a. |
Alter the gut microbiota |
PMID: 26261284; PMID: 24413286
|
Unidentified gut microbes |
Phenoxyethanol |
Therapeutic Substance |
Approved Drug |
n.a. |
cyanuric acid |
Increase Toxicity |
n.a. |
n.a. |
Microbial formation of its metabolite |
Lead to toxicity |
PMID: 26261284; PMID: 25105361
|
Faecalibacterium prausnitzii |
Tacrolimus |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Alter the pharmacokinetics of tacrolimus |
PMID: 26261284; PMID: 25815766
|
Unidentified gut microbes |
Astragali radix |
Herbal Substance |
Medicinal Herb |
n.a. |
n.a. |
n.a. |
Rat |
n.a. |
Calycosin-7-O-b-D-glucoside may alter the composition of the gut microbiome |
Promot the growth of beneficial organisms(Lactobacillus and Bifidobacterium) |
PMID: 26261284; PMID: 26101224
|
Unidentified gut microbes |
Calycosin-7-O-b-D-glucoside |
Herbal Substance |
Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
Rat |
n.a. |
Calycosin-7-O-b-D-glucoside may alter the composition of the gut microbiome |
Promot the growth of beneficial organisms(Lactobacillus and Bifidobacterium) |
PMID: 26261284; PMID: 26101224
|
Unidentified gut microbes |
Epimedium grandiflorum top (flavonoids) |
Herbal Substance |
Medicinal Herb |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Metabolized by the colonic microflora to circulate in the plasma |
[disease]osteoporosis may modulate the metabolism of Epimedii and may affect its bioavailability and efficacy |
PMID: 26135008; PMID: 26261284
|
Unidentified gut microbes |
Acetaminophen |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Microbial (p-cresol) may compete for a host enzyme (SULT1A1) |
PMID: 26261284
|
Desulfovibrio desulfuricans |
Arsenic |
Environmental Chemicals |
Toxic Agents |
n.a. |
n.a. |
Increase Toxicity |
n.a. |
n.a. |
Sulfate-reducing bacteria |
Product a more toxic form of arsenic |
PMID: 26261284
|
Firmicutes |
Butyric Acid |
Therapeutic Substance |
Investigational Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Produce relatively high levels of butyrate in the gastrointestinal tract |
Limit the growth of pathogenic microorganisms |
PMID: 26261284
|
Faecalibacterium prausnitzii |
Butyric Acid |
Therapeutic Substance |
Investigational Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Produce relatively high levels of butyrate in the gastrointestinal tract |
Limit the growth of pathogenic microorganisms |
PMID: 26261284
|
Escherichia coli |
Curcumin |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
tetrahydrocurcumin |
Increase Efficacy |
n.a. |
n.a. |
Enzyme(identified as CurA) |
n.a. |
PMID: 26261284
|
Eggerthella lenta |
Digoxin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
Decrease Efficacy |
n.a. |
n.a. |
Cardiac glycoside expressed by bacteria |
Drug is inactivated |
PMID: 26261284
|
Helicobacter pylori |
Levodopa |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Sequestration of bacteria |
Reactivated by microbially expressed enzymes |
PMID: 26261284
|
Escherichia coli |
Nitrobenzodiazepine |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
Decrease Efficacy |
n.a. |
n.a. |
Bacterial nitroreductase(NfsB) |
n.a. |
PMID: 26261284
|
Micrococcus luteus |
Polyaromatic compounds |
Environmental Chemicals |
Unclassified Substance |
n.a. |
hydroxyl metabolites |
n.a. |
n.a. |
n.a. |
n.a. |
Exhibit estrogenic activities |
PMID: 26261284
|
Clostridioides difficile |
PPIs |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Drug is associated with Clostridium difficule infections |
PMID: 26261284
|
Unidentified gut microbes |
Resveratrol |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Enzyme(identified as CurA) |
n.a. |
PMID: 26261284
|
Enterobacter |
Tretazicar |
Therapeutic Substance |
Investigational Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Additional enzymes expressed by bacteria(capable of azo and nitro reduction)((AzoR and NfsA)) |
n.a. |
PMID: 26261284
|
Staphylococcus |
Tretazicar |
Therapeutic Substance |
Investigational Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Additional enzymes expressed by bacteria(capable of azo and nitro reduction)((AzoR and NfsA)) |
n.a. |
PMID: 26261284
|
Escherichia coli |
Tretazicar |
Therapeutic Substance |
Investigational Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Additional enzymes expressed by bacteria(capable of azo and nitro reduction)((AzoR and NfsA)) |
n.a. |
PMID: 26261284
|
Mycobacterium |
Tretazicar |
Therapeutic Substance |
Investigational Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Additional enzymes expressed by bacteria(capable of azo and nitro reduction)((AzoR and NfsA)) |
n.a. |
PMID: 26261284
|
Bacillus |
Tretazicar |
Therapeutic Substance |
Investigational Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Additional enzymes expressed by bacteria(capable of azo and nitro reduction)((AzoR and NfsA)) |
n.a. |
PMID: 26261284
|
Unidentified gut microbes |
Simvastatin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Be extensively metabolized by microbiota(demethylation, carbon-carbon bond cleavage, a or b oxidation,dihydroxylation, and cyclization of simvastatin) |
n.a. |
PMID: 26261284
|
Unidentified gut microbes |
Sulfadiazine |
Therapeutic Substance |
Approved Drug |
n.a. |
5-amino 5-salicylic acid |
Increase Efficacy |
n.a. |
n.a. |
Convert drug to its pharmacologically active form by microbial enzymes |
n.a. |
PMID: 26261284
|
Unidentified gut microbes |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
SN-38 |
Increase Toxicity |
n.a. |
n.a. |
Convertion to SN-38 |
Lead to the severe intestinal side effect of diarrhea;[drug interaction:Antibiotic/a potent inhibitor of β-glucuronidase can reduce intestinal side effect] |
PMID: 26569070; PMID: 18927500
|
Unidentified gut microbes |
Acetaminophen |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
Increase Toxicity |
n.a. |
n.a. |
High level of a microbial metabolite(p-cresol) |
Show low postdose acetaminophen sulfate to acetaminophen glucuronide;alter the bioavailability;lead to hepatotoxicity;[drug interaction]:(rat)antibiotic lead to higher level of acetaminophen glutathione conjugates |
PMID: 26569070; PMID: 19667173
|
Unidentified gut microbes |
Simvastatin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Several gut microbial-derived secondary bile acids |
Secondary bile acids can predict effect of simvastatin |
PMID: 26569070; PMID: 24947972
|
Firmicutes |
Cyclophosphamide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Alter the composition of gut microbiota;induce the translocation(Gram positive bacteria)into secondary lymphoid organs |
PMID: 26569070
|
Unidentified anaerobic bacterium |
Omeprazole |
Therapeutic Substance |
Approved Drug |
n.a. |
sulfide metabolites |
Decrease Efficacy |
n.a. |
n.a. |
Reduction |
Decreased activity |
PMID: 26569070
|
Clostridioides difficile |
Acetaminophen |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
Acetaminophen sulfate and glucuronide |
Decrease Efficacy; Increase Toxicity |
n.a. |
n.a. |
O-Sulfation; C-S cleavage of acetaminophen-3-cysteine |
Decrease activity,or increase cellular toxicity |
PMID: 26569070
|
Unidentified gut microbes |
CpG-oligonucleotide immunotherapy |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
Mouse |
Germ free,orantibiotic-treated |
Disruption of gut microbiota |
Microbiota impairs the therapeutic responses of tumors |
PMID: 26569070
|
Unidentified anaerobic bacterium |
Daidzein |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
Dihydrodaidzein, equol, or O-desmethylanolensin(ODMA) |
Increase Efficacy |
n.a. |
n.a. |
Reduction, phenolic ring opening |
Increased activity |
PMID: 26569070
|
Clostridium sp. HGH 136 |
Daidzein |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
Dihydrodaidzein, equol, or O-desmethylanolensin(ODMA) |
Increase Efficacy |
n.a. |
n.a. |
Reduction, phenolic ring opening |
Increased activity |
PMID: 26569070
|
Eggerthella lenta |
Digoxin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
dihydrodigoxin |
Decrease Efficacy |
n.a. |
n.a. |
Key enzyme: A cytochrome-encoding operon (termed the cardiac glycoside reductase) |
Produce inactive metabolite |
PMID: 26569070
|
Bacteroides uniformis |
Genistein |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
5-hydroxyequol |
n.a. |
n.a. |
n.a. |
Hydrogenation |
n.a. |
PMID: 26569070
|
Bacteroides |
Ginsenoside Rb1 |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
Compound K |
Increase Efficacy |
n.a. |
n.a. |
Hydrolysis |
Increased activity |
PMID: 26569070
|
Bifidobacterium |
Ginsenoside Rb1 |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
Compound K |
Increase Efficacy |
n.a. |
n.a. |
Hydrolysis |
Increased activity |
PMID: 26569070
|
Eubacterium sp. GLH |
Glycyrrhizic acid |
Therapeutic Substance |
Approved Drug |
n.a. |
18-β-glycyrrhetinic acid |
Increase Efficacy |
n.a. |
n.a. |
Hydrolysis |
Increased activity |
PMID: 26569070
|
Klebsiella pneumoniae |
Lactulose |
Therapeutic Substance |
Approved Drug |
n.a. |
Monosaccharides |
n.a. |
n.a. |
n.a. |
Hydrolysis |
Stimulating the growth of beneficial bacteria (Bifidobacteria,Lactobacilli) |
PMID: 26569070
|
Enterococcus faecalis |
Lactulose |
Therapeutic Substance |
Approved Drug |
n.a. |
Monosaccharides |
n.a. |
n.a. |
n.a. |
Hydrolysis |
Stimulating the growth of beneficial bacteria (Bifidobacteria,Lactobacilli) |
PMID: 26569070
|
Cronobacter sakazakii |
Lactulose |
Therapeutic Substance |
Approved Drug |
n.a. |
Monosaccharides |
n.a. |
n.a. |
n.a. |
Hydrolysis |
Stimulating the growth of beneficial bacteria (Bifidobacteria,Lactobacilli) |
PMID: 26569070
|
Enterococcus casseliflavus |
Lactulose |
Therapeutic Substance |
Approved Drug |
n.a. |
Monosaccharides |
n.a. |
n.a. |
n.a. |
Hydrolysis |
Stimulating the growth of beneficial bacteria (Bifidobacteria,Lactobacilli) |
PMID: 26569070
|
Bacteroides |
Levamisole |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
levametabol-I, II and III |
Increase Efficacy |
n.a. |
n.a. |
Thiazole ring opening |
Increased activity |
PMID: 26569070
|
Clostridium sp. |
Levamisole |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
levametabol-I, II and III |
Increase Efficacy |
n.a. |
n.a. |
Thiazole ring opening |
Increased activity |
PMID: 26569070
|
Clostridia |
Metamfetamine |
Therapeutic Substance |
Approved Drug |
n.a. |
Amphetamine, norephedrine and an unknown metabolite |
Decrease Efficacy |
n.a. |
n.a. |
Demethylation |
Decreased activity |
PMID: 26569070
|
Enterococcus |
Metamfetamine |
Therapeutic Substance |
Approved Drug |
n.a. |
Amphetamine, norephedrine and an unknown metabolite |
Decrease Efficacy |
n.a. |
n.a. |
Demethylation |
Decreased activity |
PMID: 26569070
|
Lactobacillus |
Metamfetamine |
Therapeutic Substance |
Approved Drug |
n.a. |
Amphetamine, norephedrine and an unknown metabolite |
Decrease Efficacy |
n.a. |
n.a. |
Demethylation |
Decreased activity |
PMID: 26569070
|
Unidentified gut microbes |
Platinum chemotherapy |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
Mouse |
Germ free,orantibiotic-treated |
Disruption of gut microbiota |
Microbiota impairs the therapeutic responses of tumors |
PMID: 26569070
|
Enterococcus casseliflavus |
Quercetin-3-glucoside |
Herbal Substance; Dietary Substance |
Medicinal Herbal Compounds; Dietary Compounds |
n.a. |
Butyrate, acetate, 3,4-dihydroxyphenylacetic acid |
n.a. |
n.a. |
n.a. |
Deglycosylation |
n.a. |
PMID: 26569070
|
Eubacterium ramulus |
Quercetin-3-glucoside |
Herbal Substance; Dietary Substance |
Medicinal Herbal Compounds; Dietary Compounds |
n.a. |
Butyrate, acetate, 3,4-dihydroxyphenylacetic acid |
n.a. |
n.a. |
n.a. |
Deglycosylation |
n.a. |
PMID: 26569070
|
Escherichia coli |
Diclofenac |
Therapeutic Substance |
Approved Drug |
Hydrolysis to diclofenac |
Diclofenac glucuronide |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 27591027; PMID: 24780296; PMID: 22328575
|
Escherichia coli |
Flucytosine |
Therapeutic Substance |
Approved Drug |
Deamination |
5-fluorouracil |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 27591027; PMID: 12714804; PMID: 3729334
|
Unidentified anaerobic bacterium |
Digoxin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
Double bond reduction |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 6836275; PMID: 24637603; PMID: 27591027; PMID: 1500644; PMID: 2759492
|
Clostridioides difficile |
Digoxin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
Double bond reduction |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 6836275; PMID: 24637603; PMID: 27591027; PMID: 1500644; PMID: 2759492
|
Eggerthella lenta |
Digoxin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
Double bond reduction |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 6836275; PMID: 24637603; PMID: 27591027; PMID: 1500644; PMID: 2759492
|
Eggerthella lenta |
Digoxin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
Double bond reduction |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 6836275; PMID: 24637603; PMID: 27591027; PMID: 1500644; PMID: 2759492
|
Unidentified gut microbes |
Mesalazine |
Therapeutic Substance |
Approved Drug |
Acetylation |
N-acetyl-5-aminosalicylic acid |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 1425876; PMID: 27591027; PMID: 8353847; PMID: 7520936; PMID: 2890356
|
Pseudomonas aeruginosa |
Mesalazine |
Therapeutic Substance |
Approved Drug |
Acetylation |
N-acetyl-5-aminosalicylic acid |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 1425876; PMID: 27591027; PMID: 8353847; PMID: 7520936; PMID: 2890356
|
Citrobacter freundii |
Mesalazine |
Therapeutic Substance |
Approved Drug |
Acetylation |
N-acetyl-5-aminosalicylic acid |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 1425876; PMID: 27591027; PMID: 8353847; PMID: 7520936; PMID: 2890356
|
Klebsiella oxytoca |
Mesalazine |
Therapeutic Substance |
Approved Drug |
Acetylation |
N-acetyl-5-aminosalicylic acid |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 1425876; PMID: 27591027; PMID: 8353847; PMID: 7520936; PMID: 2890356
|
Klebsiella pneumoniae subsp. ozaenae |
Mesalazine |
Therapeutic Substance |
Approved Drug |
Acetylation |
N-acetyl-5-aminosalicylic acid |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 1425876; PMID: 27591027; PMID: 8353847; PMID: 7520936; PMID: 2890356
|
Morganella morganii |
Mesalazine |
Therapeutic Substance |
Approved Drug |
Acetylation |
N-acetyl-5-aminosalicylic acid |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 1425876; PMID: 27591027; PMID: 8353847; PMID: 7520936; PMID: 2890356
|
Serratia marcescens |
Mesalazine |
Therapeutic Substance |
Approved Drug |
Acetylation |
N-acetyl-5-aminosalicylic acid |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 1425876; PMID: 27591027; PMID: 8353847; PMID: 7520936; PMID: 2890356
|
Shigella flexneri |
Mesalazine |
Therapeutic Substance |
Approved Drug |
Acetylation |
N-acetyl-5-aminosalicylic acid |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 1425876; PMID: 27591027; PMID: 8353847; PMID: 7520936; PMID: 2890356
|
Vibrio cholerae |
Mesalazine |
Therapeutic Substance |
Approved Drug |
Acetylation |
N-acetyl-5-aminosalicylic acid |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 1425876; PMID: 27591027; PMID: 8353847; PMID: 7520936; PMID: 2890356
|
Plesiomonas shigelloides |
Mesalazine |
Therapeutic Substance |
Approved Drug |
Acetylation |
N-acetyl-5-aminosalicylic acid |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 1425876; PMID: 27591027; PMID: 8353847; PMID: 7520936; PMID: 2890356
|
Citrobacter amalonaticus |
Mesalazine |
Therapeutic Substance |
Approved Drug |
Acetylation |
N-acetyl-5-aminosalicylic acid |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 1425876; PMID: 27591027; PMID: 8353847; PMID: 7520936; PMID: 2890356
|
Klebsiella pneumoniae subsp. rhinoscleromatis |
Mesalazine |
Therapeutic Substance |
Approved Drug |
Acetylation |
N-acetyl-5-aminosalicylic acid |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 1425876; PMID: 27591027; PMID: 8353847; PMID: 7520936; PMID: 2890356
|
Citrobacter farmeri |
Mesalazine |
Therapeutic Substance |
Approved Drug |
Acetylation |
N-acetyl-5-aminosalicylic acid |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 1425876; PMID: 27591027; PMID: 8353847; PMID: 7520936; PMID: 2890356
|
Clostridium sporogenes |
Zonisamide |
Therapeutic Substance |
Approved Drug |
Benzisoxazole ring reduction |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 27591027; PMID: 9231340; PMID: 1615700
|
Unidentified gut microbes |
Ranitidine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
N-oxide reduction |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 27591027; PMID: 11564550
|
Unidentified gut microbes |
Nizatidine |
Therapeutic Substance |
Approved Drug |
N-oxide reduction |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 27591027; PMID: 11955801
|
Bacteroides |
Levamisole |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
Thiazole ring opening |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 27591027; PMID: 1949905
|
Clostridium sp. |
Levamisole |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
Thiazole ring opening |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 27591027; PMID: 1949905
|
Unidentified anaerobic bacterium |
Fostamatinib |
Therapeutic Substance |
Approved Drug |
O-Demethylation |
metabolite R529 |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 27591027; PMID: 20371637
|
Unidentified gut microbes |
Sulfapyridine |
Therapeutic Substance |
Approved Drug |
Acetylation |
N-acetyl sulfapyridine |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 27591027; PMID: 2890356
|
Unidentified anaerobic bacterium |
Sulfinpyrazone |
Therapeutic Substance |
Approved Drug |
Sulfoxide reduction |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 27591027; PMID: 3630204
|
Unidentified anaerobic bacterium |
Sulindac |
Therapeutic Substance |
Approved Drug |
Sulfoxide reduction |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 27591027; PMID: 3630204
|
Escherichia coli |
Irinotecan |
Therapeutic Substance |
Approved Drug |
Glucuronide hydrolysis |
SN-38 glucuronide |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 16437251; PMID: 26364932; PMID: 9744772; PMID: 11344150; PMID: 27591027
|
Bacteroides fragilis |
Irinotecan |
Therapeutic Substance |
Approved Drug |
Glucuronide hydrolysis |
SN-38 glucuronide |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 16437251; PMID: 26364932; PMID: 9744772; PMID: 11344150; PMID: 27591027
|
Streptococcus agalactiae |
Irinotecan |
Therapeutic Substance |
Approved Drug |
Glucuronide hydrolysis |
SN-38 glucuronide |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 16437251; PMID: 26364932; PMID: 9744772; PMID: 11344150; PMID: 27591027
|
Clostridium perfringens |
Irinotecan |
Therapeutic Substance |
Approved Drug |
Glucuronide hydrolysis |
SN-38 glucuronide |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 16437251; PMID: 26364932; PMID: 9744772; PMID: 11344150; PMID: 27591027
|
Unidentified gut microbes |
3,4-Dihydro-5-Methyl-Isoquinolinone |
Therapeutic Substance |
Investigational Drug |
n.a. |
n.a. |
n.a. |
Mouse |
Convention and germ-free |
n.a. |
DHQ production was dependent on bacteria |
PMID: 27782392; PMID: 19234110
|
Unidentified gut microbes |
Simvastatin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Drug modulate or interact with the microbiota |
PMID: 21060933; PMID: 27782392
|
Unidentified gut microbes |
Hippuric acid |
Environmental Chemicals |
Industrial Chemicals and Pollutants; Toxic Agents |
n.a. |
n.a. |
Increase Efficacy |
Mouse |
Germ-free,or with antibiotics |
n.a. |
Drug concentration in urine is reduced in either germ-free mice or in mice treated with antibiotics |
PMID: 27782392; PMID: 23342949
|
Unidentified gut microbes |
Metformin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
Mouse |
n.a. |
Increase hat fatty acid metabolism |
Contribute to metformin therapy |
PMID: 25038099; PMID: 27782392
|
Unidentified gut microbes |
Metformin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Drug modulate or interact with the microbiota |
PMID: 25038099; PMID: 27782392
|
Unidentified gut microbes |
Levocarnitine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
TMA, TMAO |
n.a. |
n.a. |
n.a. |
L-carnitine is metabolized to TMA by microbiota |
Decrease AGE levels |
PMID: 25636076; PMID: 27782392
|
Unidentified gut microbes |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
Increase Toxicity |
n.a. |
n.a. |
Β-glucuronidase enzyme of bacteria |
Cause gut inflammation and irritation;drug interaction:irinotecan with a β-glucuronidase inhibitor decreases harmful metabolites and alleviates the gastrointestinal inflammation |
PMID: 27782392; PMID: 26364932
|
Unidentified gut microbes |
Levodopa |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
m-tyramine |
n.a. |
Mouse |
Germ-free |
n.a. |
(GF mice)reduce metabolism of L-DOPA,prolong L-DOPA half-life and hence activity |
PMID: 4974346; PMID: 27782392
|
Escherichia sp. |
Metformin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
Increase Toxicity |
n.a. |
n.a. |
Cause an increase of Escherichia spp |
Result in an increase of gas metabolism pathways(side effect of metformin) |
PMID: 27782392
|
Pseudomonas aeruginosa |
2,8-DHQ (including 2,4-DHQ) |
Environmental Chemicals |
Human Metabolite |
n.a. |
n.a. |
Increase Toxicity |
n.a. |
n.a. |
n.a. |
Drug is involved in the pathogenicity of bacteria |
PMID: 27782392
|
Enterobacteriaceae |
Aspartame |
Therapeutic Substance; Dietary Substance; Herbal Substance |
Dietary Compounds; Artificial Sweetener; Medicinal Herbal Compounds |
n.a. |
SCFA(propionate) |
n.a. |
Rat |
n.a. |
n.a. |
Aspartame increased total bacteria |
PMID: 27782392
|
[Clostridium] leptum |
Aspartame |
Therapeutic Substance; Dietary Substance; Herbal Substance |
Dietary Compounds; Artificial Sweetener; Medicinal Herbal Compounds |
n.a. |
SCFA(propionate) |
n.a. |
Rat |
n.a. |
n.a. |
Aspartame increased total bacteria |
PMID: 27782392
|
Bifidobacterium |
B-GOSr (prebiotic oligosaccharide) |
Therapeutic Substance |
n.a. |
n.a. |
SCFA(acetate) |
n.a. |
Human |
n.a. |
n.a. |
Bacteria populations increases acetate |
PMID: 27782392
|
Clostridia |
Choline |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
trimethylamine (TMA) |
n.a. |
n.a. |
n.a. |
n.a. |
Have a direct relationship to cardiovascular disease and atherosclerosis |
PMID: 27782392
|
Eggerthella lenta |
Digoxin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
dihydrodigoxin |
Decrease Efficacy |
n.a. |
n.a. |
The cgr operon within strains of E. lenta reduce fumarate in E. lenta to reduce digoxin |
Lack cardiac activity |
PMID: 27782392
|
Bacteroides |
Lactulose |
Therapeutic Substance |
Approved Drug |
n.a. |
lactic acid,acetic acid |
Increase Efficacy |
n.a. |
n.a. |
n.a. |
Produce its therapeutic metabolites |
PMID: 27782392
|
Bifidobacterium |
Lactulose |
Therapeutic Substance |
Approved Drug |
n.a. |
lactic acid,acetic acid |
Increase Efficacy |
n.a. |
n.a. |
n.a. |
Produce its therapeutic metabolites |
PMID: 27782392
|
Clostridia |
Sodium cyclamate |
Dietary Substance |
Dietary Compounds; Artificial Sweetener |
n.a. |
cyclohexylamine |
n.a. |
Human; Mouse |
n.a. |
n.a. |
Drug interaction:antibiotic treatment reduce cyclohexylamine production |
PMID: 27782392
|
Enterococcus |
Sodium cyclamate |
Dietary Substance |
Dietary Compounds; Artificial Sweetener |
n.a. |
cyclohexylamine |
n.a. |
Human; Mouse |
n.a. |
n.a. |
Drug interaction:antibiotic treatment reduce cyclohexylamine production |
PMID: 27782392
|
Unidentified gut microbes |
3,3-dimethyl-1-butanol |
Environmental Chemicals |
Unclassified Substance |
n.a. |
TMA, TMAO |
n.a. |
Mouse |
n.a. |
n.a. |
Drug interaction:inhibition of TMA lyase inhibits microbial production of TMA, reducing TMAO levels |
PMID: 27782392
|
Unidentified gut microbes |
Arabinoxylan-oligosaccharides |
Environmental Chemicals |
Unclassified Substance |
n.a. |
SCFA; phenol, pcresol |
n.a. |
Human |
n.a. |
n.a. |
AXOS supplementation has a long-term effect on colonic microbe community |
PMID: 27782392
|
Unidentified gut microbes |
Aryl hydrocarbon receptor activator |
Environmental Chemicals |
Industrial Chemicals and Pollutants; Toxic Agents |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Alter the gut microbiota community its metabolic function |
PMID: 27782392
|
Unidentified gut microbes |
Ellagic acid |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Alter the gut microbiota community its metabolic function |
PMID: 27782392
|
Unidentified gut microbes |
Arsenic |
Environmental Chemicals |
Toxic Agents |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Alter the gut microbiota community its metabolic function |
PMID: 27782392
|
Escherichia coli |
NSAIDs |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
Increase Toxicity |
n.a. |
n.a. |
Cleave the glucuronide by bacteria |
Yield harmful metabolites,cause the formation of ulcers in the gut; |
PMID: 27782392
|
Unidentified gut microbes |
Persistent organic pollutant |
Environmental Chemicals |
Industrial Chemicals and Pollutants |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Alter the gut microbiota community its metabolic function |
PMID: 27782392
|
Unidentified gut microbes |
Rifaximin |
Therapeutic Substance |
Approved Drug |
n.a. |
Hippuric acid |
n.a. |
Mouse |
n.a. |
n.a. |
Drug interaction:antibiotic(rifaximin)decreases microbial metabolites(hippuric acid) |
PMID: 27782392
|
Lactobacillus |
Tempol |
Therapeutic Substance |
Investigational Drug |
n.a. |
TβMCA |
n.a. |
Mouse |
n.a. |
n.a. |
Tempol reduces BSH activity of bacteria and produces antiobesity effects |
PMID: 27782392
|
Unidentified gut microbes |
Oxaliplatin |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Immunomodulation |
Mediated by TLR4 and reactive oxygen species production by myeloid cells |
PMID: 18555978; PMID: 28270698
|
Mycoplasma |
Floxuridine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
Decrease Efficacy |
n.a. |
n.a. |
Enzymatic degradation |
Mycoplasma encoded nucleoside phosphorylases restrict cytostatic activity |
PMID: 28270698
|
Mycoplasma |
Trifluridine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
Decrease Efficacy |
n.a. |
n.a. |
Enzymatic degradation |
Mycoplasma encoded nucleoside phosphorylases restrict cytostatic activity |
PMID: 28270698
|
Bifidobacterium |
Anti-PD-L1 therapy |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Immunomodulation |
Tumour‑specific T‑cell induction;increase T cells in tumour microenvironment |
PMID: 28270698
|
Proteobacteria |
Carmustine, Etoposide, Cytarabine and melphalan combination |
Therapeutic Substance |
Drug Combination |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Reduced diversity; ecological network function |
Chemotherapy associated with reduction in bacteria that limit inflammation and increase in bacteria associated with colitis |
PMID: 28270698
|
Firmicutes |
Carmustine, Etoposide, Cytarabine and melphalan combination |
Therapeutic Substance |
Drug Combination |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Reduced diversity; ecological network function |
Chemotherapy associated with reduction in bacteria that limit inflammation and increase in bacteria associated with colitis |
PMID: 28270698
|
Actinobacteria |
Carmustine, Etoposide, Cytarabine and melphalan combination |
Therapeutic Substance |
Drug Combination |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Reduced diversity; ecological network function |
Chemotherapy associated with reduction in bacteria that limit inflammation and increase in bacteria associated with colitis |
PMID: 28270698
|
Ruminococcus |
CpG oligodeoxynucleotides |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Immunomodulation |
Priming of tumour‑associated myeloid inflammatory responses |
PMID: 28270698
|
Alistipes |
CpG oligodeoxynucleotides |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Immunomodulation |
Priming of tumour‑associated myeloid inflammatory responses |
PMID: 28270698
|
Bacteroidales |
CTLA-4 blockade |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Immunomodulation |
Decreased activation of splenic effector CD4 + T cells and tumour‑infiltrating lymphocytes |
PMID: 28270698
|
Segmented filamentous bacteria |
Cyclophosphamide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Immunomodulation |
Gram‑positive commensals mediate accumulation of TH 17 and TH 1‑cell response |
PMID: 28270698
|
Lactobacillus |
Cyclophosphamide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Immunomodulation |
Gram‑positive commensals mediate accumulation of TH 17 and TH 1‑cell response |
PMID: 28270698
|
Enterococcus hirae |
Cyclophosphamide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Translocation |
Commensal bacteria cross the intestinal barrier to enter secondary lymphoid organs |
PMID: 28270698
|
Lactobacillus murinus |
Cyclophosphamide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Translocation |
Commensal bacteria cross the intestinal barrier to enter secondary lymphoid organs |
PMID: 28270698
|
Lactobacillus johnsonii |
Cyclophosphamide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Translocation |
Commensal bacteria cross the intestinal barrier to enter secondary lymphoid organs |
PMID: 28270698
|
Enterococcus hirae |
Doxorubicin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Translocation |
Commensal bacteria cross the intestinal barrier to enter secondary lymphoid organs |
PMID: 28270698
|
Lactobacillus murinus |
Doxorubicin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Translocation |
Commensal bacteria cross the intestinal barrier to enter secondary lymphoid organs |
PMID: 28270698
|
Lactobacillus johnsonii |
Doxorubicin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Translocation |
Commensal bacteria cross the intestinal barrier to enter secondary lymphoid organs |
PMID: 28270698
|
Mycoplasma |
Gemcitabine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
Decrease Efficacy |
n.a. |
n.a. |
Enzymatic degradation |
Mycoplasma encoded nucleoside phosphorylases restrict cytostatic activity |
PMID: 28270698
|
Bacteroidetes |
Ipilimumab |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
Increase Toxicity |
n.a. |
n.a. |
n.a. |
Bacterially mediated B vitamin production and polyamine transport deficiencies associated with increased risk of CTLA‑4 blockade‑induced colitis |
PMID: 28270698
|
Unidentified gut microbes |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
Increase Efficacy; Increase Toxicity |
n.a. |
n.a. |
Enzymatic degradation |
Bacterial β‑glucuronidase cleaves glucuronide from inactive metabolite, releasing active metabolite (SN‑38) in the gut |
PMID: 28270698
|
Bacteroides |
Methotrexate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Reduced diversity; ecological network function |
Reduced diversity and shifts in relative abundance associated with chemotherapy‑induced diarrhoea |
PMID: 28270698
|
Streptococcus |
Methotrexate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Reduced diversity; ecological network function |
Reduced diversity and shifts in relative abundance associated with chemotherapy‑induced diarrhoea |
PMID: 28270698
|
Unidentified gut microbes |
Mesalazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
N-acetylation by microbial N-acetyltransferases |
Yield a inactive metabolite |
PMID: 11344150; PMID: 28642381
|
Unidentified gut microbes |
Sulfasalazine |
Therapeutic Substance |
Approved Drug |
n.a. |
sulfapyridine;5-ASA;N-acetyl 5-ASA |
Decrease Efficacy |
n.a. |
n.a. |
Reduce |
Lack anti-inflammatory |
PMID: 1425876; PMID: 28642381
|
Unidentified gut microbes |
Ginsenosides |
Therapeutic Substance |
Investigational Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Inhibit cytochrome P-450s;affect host xenobiotic metabolism |
PMID: 16547074; PMID: 28642381
|
Unidentified gut microbes |
Tryptophan |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
antioxidant indole-3-propionic acid;the neurotransmitter tryptamine;indole |
Increase Toxicity |
n.a. |
n.a. |
n.a. |
Generate the uremic toxin indoxyl sulfate |
PMID: 17146590; PMID: 28642381
|
Unidentified gut microbes |
Cysteine-S-conjugates of xenobiotics |
Environmental Chemicals |
Unclassified Substance |
n.a. |
thiol metabolites |
n.a. |
n.a. |
n.a. |
Cleave cysteine-S-conjugates of polychlorinated biphenyls by C-S β-lyases |
Serve as a sole nitrogen,a potential role in nutrient acquisition |
PMID: 20306345; PMID: 28642381
|
Unidentified gut microbes |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
Increase Toxicity |
n.a. |
n.a. |
Β-glucuronidase enzymes hydrolyze SN-38G;regenerate active agent |
Cause intestinal damage and severe diarrhea;drug interaction:inhibitors |
PMID: 21051639; PMID: 28642381
|
Unidentified gut microbes |
Berberine |
Herbal Substance |
Medicinal Herbal Compounds |
n.a. |
n.a. |
Increase Bioavailability |
n.a. |
n.a. |
n.a. |
Allow intestinal absorption |
PMID: 26174047; PMID: 28642381
|
Unidentified gut microbes |
Sulfoxide |
Environmental Chemicals |
Unclassified Substance |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Reduce the sulfoxide |
n.a. |
PMID: 3630204; PMID: 28642381
|
Unidentified gut microbes |
Azo dyes |
Environmental Chemicals |
Industrial Chemicals and Pollutants |
n.a. |
mutagenic bis-aniline benzidine |
Increase Toxicity |
Conventional mice(not GF) |
n.a. |
n.a. |
Increase carcinogen exposure |
PMID: 3726894; PMID: 28642381
|
Unidentified gut microbes |
Methylmercury |
Environmental Chemicals |
Industrial Chemicals and Pollutants; Toxic Agents |
n.a. |
inorganic mercury |
Decrease Toxicity |
Rat |
n.a. |
n.a. |
Lead to less toxicity,facilitate mercury excretion |
PMID: 626001; PMID: 28642381
|
Unidentified gut microbes |
Amygdalin |
Herbal Substance; Dietary Substance |
Medicinal Herbal Compounds; Dietary Compounds |
n.a. |
mandelonitrile |
Increase Toxicity |
n.a. |
n.a. |
Hydrolyze the glycosidic linkage |
Produce benzaldehydy and toxic cyanide |
PMID: 7362642; PMID: 28642381
|
Unidentified gut microbes |
Loperamide |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Reduce the N-oxide |
n.a. |
PMID: 7628301; PMID: 28642381
|
Eggerthella lenta |
Digoxin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
dihydrodigoxin |
n.a. |
Human; GF mice |
n.a. |
Flavin-dependent reductase(Cgr2) |
n.a. |
PMID: 28642381
|
Escherichia coli |
Anticancer drugs |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Increase or decrease the efficacy of drug |
PMID: 28642381
|
Listeria welshimeri |
Anticancer drugs |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Increase or decrease the efficacy of drug |
PMID: 28642381
|
Escherichia coli |
CB954 |
Environmental Chemicals |
Unclassified Substance |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Direct chemical modification |
n.a. |
PMID: 28642381
|
Escherichia coli |
Fludarabine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Direct chemical modification |
n.a. |
PMID: 28642381
|
Escherichia coli |
Gemcitabine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Direct chemical modification |
n.a. |
PMID: 28642381
|
Lactobacillus brevis |
Levodopa |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
mtyramine |
n.a. |
n.a. |
n.a. |
Microbial decarboxylation and p-dehydroxylation(a tyrosine decarboxylase accepts L-dopa in vitro) |
Contribute to the substantial variation |
PMID: 28642381
|
Klebsiella |
Phenoxyethanol |
Therapeutic Substance |
Approved Drug |
n.a. |
cyanuric acid |
Increase Toxicity |
Mouse |
n.a. |
Deaminate |
Lead to renal toxicity |
PMID: 28642381
|
Pseudomonas aeruginosa |
Gluten |
Dietary Substance |
Dietary Compounds |
n.a. |
n.a. |
n.a. |
Mouse |
n.a. |
n.a. |
Elicit an enhanced gluten-specific immune response(compare with peptieds produced by Lactobacillus spp.from healthy individuals) |
PMID: 28642381
|
Unidentified gut microbes |
Thiazolidinediones |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
Rat |
Diet-induced obesity |
n.a. |
Indirectlyaffect gut bacteria(HFD leads to an increase in the relative abundance of Proteobacteria) |
PMID: 27751827; PMID: 28973971
|
Unidentified gut microbes |
Acarbose |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
Human |
Patients with hyperlipidemia or T2D |
Prevent starch processing and absorption; |
Enhance starch-fermenting and butyrate-producing bacteria;inhibit starch use by propionate-producing bacteria;increase Lactobacillus,Bifidobacterium and other SCFA-producing bacteria;associated with a diminution of Enterobacteriaceae,Bacteroidaceae and lecithinase positive Clostridum in human feces |
PMID: 28973971
|
Escherichia coli |
Acarbose |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Affect nutrient sources of bacteria |
Block the growth of E.coli |
PMID: 28973971
|
SCFA-producing bacteria |
Antidiabetic drugs |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Positively influence the bacteria |
PMID: 28973971
|
SCFA-producing bacteria |
High-fiber diets |
Dietary Substance |
Dietary Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Positively influence the bacteria |
PMID: 28973971
|
Unidentified gut microbes |
Incretin |
Environmental Chemicals |
Human Metabolite |
n.a. |
n.a. |
n.a. |
Primary murine colonic culture |
n.a. |
Microbiota fermentation products |
Influence incretin secretion |
PMID: 28973971
|
Unidentified gut microbes |
Liraglutide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Mouse |
High-fat diet(HFD),HF-fed,diabetes-induced |
n.a. |
Enrich Firmicutes;deplete Bacteroidetes,Proteobacteria and Actinobacteria phyla;enrich 13 phylotypes(Allobaculum,Turicibacter,Anaerostipes,Blautia,Lactobacillus,Butyricimonas,Desulfovibrio);decrease 20 phylotypes in the orders Clostridiales and Bacteroidales |
PMID: 28973971
|
Escherichia |
Metformin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
Human |
n.a. |
Inhibit the dihydrofolate reductase activity of bacteria |
Influence the side-effects of drug |
PMID: 28973971
|
Bacteroides |
Metformin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
SCFA-producing bacteria |
Enric the bacteria |
PMID: 28973971
|
Lactobacillus |
Metformin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Positive effects |
PMID: 28973971
|
Phascolarctobacterium |
Metformin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
SCFA-producing bacteria |
Enric the bacteria |
PMID: 28973971
|
Blautia |
Metformin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
SCFA-producing bacteria |
Enric the bacteria |
PMID: 28973971
|
Butyricicoccus |
Metformin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
SCFA-producing bacteria |
Enric the bacteria |
PMID: 28973971
|
Bacteroidetes |
Metformin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
Mouse |
High-fat diet(HFD) |
n.a. |
Decrease bacterial diversity |
PMID: 28973971
|
Proteobacteria |
Metformin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Positive effects |
PMID: 28973971
|
Firmicutes |
Metformin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
Mouse |
High-fat diet(HFD) |
n.a. |
Decrease bacterial diversity |
PMID: 28973971
|
Verrucomicrobia |
Metformin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
Mouse |
High-fat diet(HFD) |
Genus Akkermansia |
Increase the relative abundance of bacteria |
PMID: 28973971
|
Bifidobacterium adolescentis |
Metformin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Promote bacteria growth |
Contribute to the glucose-lowering effect |
PMID: 28973971
|
Allobaculum |
Metformin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Positive effects |
PMID: 28973971
|
Coriobacteriaceae |
Miglitol |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Mouse |
A high fat and high glucose diet |
Suppression of intestinal inflammation |
Reverse the increase of bacteria |
PMID: 28973971
|
Erysipelotrichaceae |
Miglitol |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Mouse |
A high fat and high glucose diet |
Suppression of intestinal inflammation |
Reverse the increase of bacteria |
PMID: 28973971
|
SCFA-producing bacteria |
Physical activity |
Environmental Chemicals |
Unclassified Substance |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Positively influence the bacteria |
PMID: 28973971
|
Proteobacteria |
Pioglitazone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Rat |
High-fat diet(HFD) |
Correlate with the decrease of plasma endotoxin, TNF-α , IL-6 and MCP-1 levels |
Reduce the abundance of bacteria |
PMID: 28973971
|
Unidentified gut microbes |
Saxagliptin |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Mouse |
HF-fed,diabetic-induced |
n.a. |
Enrich Firmicutes,mainly the genera Lactobacillus,Allobaculum and Turicibacter;contain less Bacteroides and Prevotella;decrease the phylum Bacteroidetes |
PMID: 28973971
|
Unidentified gut microbes |
Sitagliptin |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Rat |
Diabetes-induced |
n.a. |
Increase in the relative abundance of Bacteroidetes and Proteobacteria;decrease Firmicute;influence SCFA-producing bacteria;Lactobacillus and Bifidobacterium are depleted in feces |
PMID: 28973971
|
Unidentified gut microbes |
Voglibose |
Therapeutic Substance |
Investigational Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Decrease the Firmicutes to Bacteroidetes ratio and higher the abundance in Verrucomicrobia |
PMID: 28973971
|
Unidentified gut microbes |
Mesalazine |
Therapeutic Substance |
Approved Drug |
n.a. |
acetylated 5-aminosalicylic acid |
Increase Efficacy |
n.a. |
n.a. |
N-acetyltransferases from bacteria |
Exert physiopathological effects,increase activity |
PMID: 11344150; PMID: 30227749
|
Unidentified gut microbes |
Ranitidine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Lead to poor bioavailability of ranitidine |
PMID: 11564550; PMID: 30227749
|
Unidentified gut microbes |
Morphine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
Increase Toxicity |
n.a. |
n.a. |
Hydrolysis of glucuronide |
Increase drug toxicity |
PMID: 1185599; PMID: 30227749
|
Unidentified gut microbes |
Nizatidine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
Decrease Efficacy |
n.a. |
n.a. |
N-oxide bond cleavage |
Decrease activity |
PMID: 30227749; PMID: 11955801
|
Unidentified gut microbes |
Lovastatin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
M1 (demethylbutyryl metabolite), M4 (hydroxylated metabolite), M8 (the active hydroxy acid metabolite), and M9 (hydroxylated M8) |
n.a. |
Human; Rat |
n.a. |
n.a. |
Produce four metabolites |
PMID: 30227749; PMID: 24947972
|
Unidentified gut microbes |
Deleobuvir |
Therapeutic Substance |
Investigational Drug |
n.a. |
CD 6168 |
n.a. |
n.a. |
n.a. |
An alkene reduction by the gut microbiota |
n.a. |
PMID: 30227749; PMID: 26068924
|
Unidentified gut microbes |
Amlodipine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
Increase Efficacy |
n.a. |
n.a. |
n.a. |
Increase activity |
PMID: 30227749; PMID: 26630218
|
Unidentified gut microbes |
Epacadostat |
Therapeutic Substance |
Investigational Drug |
n.a. |
Amidine metabolite |
Decrease Efficacy |
n.a. |
n.a. |
n.a. |
Decrease activity |
PMID: 30227749; PMID: 27457784
|
Unidentified gut microbes |
Chloramphenicol |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
Increase Toxicity |
n.a. |
n.a. |
Amine formation |
n.a. |
PMID: 30227749; PMID: 4165044
|
Unidentified gut microbes |
Sulfanilamide |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
Increase Toxicity |
n.a. |
n.a. |
Azoreductase enzymes,Activation of azo-bond containing prodrug to sulfanilamid |
Increase toxicity |
PMID: 5173017; PMID: 30227749
|
Unidentified gut microbes |
Sulfonamide antibiotics |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Microbial transformation |
n.a. |
PMID: 5173017; PMID: 30227749
|
Unidentified gut microbes |
Clonazepam |
Therapeutic Substance |
Approved Drug |
n.a. |
7-aminoclonazepam |
Increase Toxicity |
n.a. |
n.a. |
Nitro reduction |
n.a. |
PMID: 6506755; PMID: 30227749
|
Unidentified gut microbes |
Risperidone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
Decrease Efficacy |
n.a. |
n.a. |
Isoxazole scission or hydroxylation |
Decrease activity |
PMID: 7512019; PMID: 30227749
|
Unidentified gut microbes |
Loperamide oxide |
Therapeutic Substance |
Investigational Drug |
n.a. |
active drug loperamide |
Increase Efficacy |
Human; Dog; Rat |
n.a. |
n.a. |
Make the metabolism and increase activity of loperamide oxide |
PMID: 7628301; PMID: 30227749
|
Unidentified gut microbes |
Omeprazole |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
No alteration of pharmacokinetics |
PMID: 7629748; PMID: 30227749
|
Unidentified gut microbes |
Calcitonin |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Susceptible to proteolysis,Protease |
Increase large-intestinal absorption,decrease activity |
PMID: 30227749; PMID: 9055189
|
Unidentified gut microbes |
Insulin human |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Susceptible to proteolysis,Protease |
Increase large-intestinal absorption,decrease activity |
PMID: 30227749; PMID: 9055189
|
Unidentified gut microbes |
Cimetidine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Influence drug delivery and absorption |
PMID: 30227749
|
Unidentified gut microbes |
Famotidine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Influence drug delivery and absorption |
PMID: 30227749
|
Unidentified gut microbes |
Nizatidine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Influence drug delivery and absorption |
PMID: 30227749
|
Bacteroides |
Sorivudine |
Therapeutic Substance |
Investigational Drug |
n.a. |
(E)-5-(2-bromovinyl)uracil |
Decrease Efficacy |
n.a. |
n.a. |
n.a. |
Reduce activity |
PMID: 30227749
|
Clostridioides difficile |
Acetaminophen |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
Decrease Efficacy; Increase Toxicity |
n.a. |
n.a. |
P-cresol(microbial metabolite) reduces metabolic clearance |
Reduce activity;delay the metabolism of drug in the human body and increase risk of hepatotoxicity |
PMID: 30227749
|
Enterobacteriales |
Acetylsalicylic acid |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
Increase Efficacy |
n.a. |
n.a. |
n.a. |
Modulate the metabolism and pharmacokinetics;Potentiate the therapeutic potency |
PMID: 30227749
|
Enterococcus |
Acetylsalicylic acid |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
Increase Efficacy |
n.a. |
n.a. |
n.a. |
Modulate the metabolism and pharmacokinetics;Potentiate the therapeutic potency |
PMID: 30227749
|
Lactobacillus |
Acetylsalicylic acid |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
Increase Efficacy |
n.a. |
n.a. |
n.a. |
Modulate the metabolism and pharmacokinetics;Potentiate the therapeutic potency |
PMID: 30227749
|
Escherichia coli Nissle 1917 |
Amiodarone |
Therapeutic Substance |
Approved Drug |
n.a. |
DEA |
Increase Efficacy; Increase Bioavailability |
Animal model |
n.a. |
n.a. |
Increase bioavailability of AMI,increase plasma levels of desethylamiodarone(DEA),promote the absorption of AMI and increase the activity of CYP2C |
PMID: 30227749
|
Clostridium sp. |
Balsalazide |
Therapeutic Substance |
Approved Drug |
n.a. |
5-aminosalicylic acid |
Increase Toxicity |
n.a. |
n.a. |
Reduction and Release of 5-aminosalicylic acid;Azoreductases |
Increase toxicity |
PMID: 30227749
|
Eggerthella lenta |
Digoxin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
digoxigenin,or dihydrodigoxin |
Decrease Efficacy |
human |
n.a. |
Reduction |
Produce inactive metabolites;[interaction]:(gnotobiotic mice)dietary protein reduces microbial metabolism of digoxin(vivo) and changes drug concentration(in the serum and urine);[drug interaction]:antibiotics(tetracycline or erythromycin) increase plasma concentration of digoxin |
PMID: 30227749
|
Bacteroides |
Glucuronides |
Environmental Chemicals |
Unclassified Substance |
n.a. |
diclofenac,ketoprofen,indomethacin |
Increase Toxicity |
n.a. |
n.a. |
Hydrolysis of the glycosidicbon |
Increase toxicity |
PMID: 30227749
|
Clostridium |
Glucuronides |
Environmental Chemicals |
Unclassified Substance |
n.a. |
diclofenac,ketoprofen,indomethacin |
Increase Toxicity |
n.a. |
n.a. |
Hydrolysis of the glycosidicbon |
Increase toxicity |
PMID: 30227749
|
Bifidobacterium sp. |
Glucuronides |
Environmental Chemicals |
Unclassified Substance |
n.a. |
diclofenac,ketoprofen,indomethacin |
Increase Toxicity |
n.a. |
n.a. |
Hydrolysis of the glycosidicbon |
Increase toxicity |
PMID: 30227749
|
Escherichia coli |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
SN-38 |
Increase Toxicity |
n.a. |
n.a. |
Hydrolysis of the glycosidicbon,bacterial b-glucuronidases |
Increase toxicity |
PMID: 30227749
|
Bacteroides vulgatus |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
SN-38 |
Increase Toxicity |
n.a. |
n.a. |
Hydrolysis of the glycosidicbon,bacterial b-glucuronidases |
Increase toxicity |
PMID: 30227749
|
Erysipelatoclostridium ramosum |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
SN-38 |
Increase Toxicity |
n.a. |
n.a. |
Hydrolysis of the glycosidicbon,bacterial b-glucuronidases |
Increase toxicity |
PMID: 30227749
|
Bacteroides |
Lactulose |
Therapeutic Substance |
Approved Drug |
n.a. |
lactic and acetic acidsactive metabolite |
Decrease Efficacy |
n.a. |
n.a. |
n.a. |
Reduce activity |
PMID: 30227749
|
Clostridium |
Lactulose |
Therapeutic Substance |
Approved Drug |
n.a. |
lactic and acetic acidsactive metabolite |
Decrease Efficacy |
n.a. |
n.a. |
n.a. |
Reduce activity |
PMID: 30227749
|
Lactobacillus |
Lactulose |
Therapeutic Substance |
Approved Drug |
n.a. |
lactic and acetic acidsactive metabolite |
Decrease Efficacy |
n.a. |
n.a. |
n.a. |
Reduce activity |
PMID: 30227749
|
Bacteroides |
Levamisole |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
Increase Efficacy |
n.a. |
n.a. |
Thiazole ring opening |
Increase activity |
PMID: 30227749
|
Clostridium sp. |
Levamisole |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
Increase Efficacy |
n.a. |
n.a. |
Thiazole ring opening |
Increase activity |
PMID: 30227749
|
Unidentified gut microbes |
Levodopa |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Catalyze p-dehydroxylation of L-dopa to mhydroxyphenylacetic acid |
n.a. |
PMID: 30227749
|
Helicobacter pylori |
Levodopa |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
Decrease Bioavailability |
Human |
Patients with Parkinson’s disease (PD) |
Dehydroxylation |
Reduce acute L-dopa absorption;reduce L-dopa onset time, ON duration, motor severity, and quality of life parameters |
PMID: 30227749
|
Clostridium perfringens |
Metronidazole |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
N-(2-hydroxyethyl)-oxamic acid and acetamide |
Decrease Efficacy |
n.a. |
n.a. |
Reduction |
Reduce activity |
PMID: 30227749
|
[Clostridium] leptum |
Nitrazepam |
Therapeutic Substance |
Approved Drug |
n.a. |
7-acetylaminonitrazepam |
Decrease Toxicity |
n.a. |
n.a. |
Nitroreductase |
Produce teratogenic activity metabolites,Induce teratogenicity |
PMID: 30227749
|
Clostridium sp. |
Olsalazine |
Therapeutic Substance |
Approved Drug |
n.a. |
5-aminosalicylic acid |
Increase Toxicity |
n.a. |
n.a. |
Reduction and Release of 5-aminosalicylic acid;Azoreductases |
Increase toxicity |
PMID: 30227749
|
Lactobacillus |
Simvastatin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Affect the pharmacokinetics and pharmacodynamics;increase the risk of myopathy |
PMID: 30227749
|
Clostridium sp. |
Sulfasalazine |
Therapeutic Substance |
Approved Drug |
n.a. |
5-aminosalicylic acid |
Increase Toxicity |
n.a. |
n.a. |
Reduction and Release of 5-aminosalicylic acid;Azoreductases |
Increase toxicity |
PMID: 30227749
|
Clostridium sporogenes |
Zonisamide |
Therapeutic Substance |
Approved Drug |
n.a. |
2-sulphamoylacetylphenol |
Increase Efficacy |
n.a. |
n.a. |
Zonisamide reductase |
Increase activity |
PMID: 30227749
|
Pseudomonas fluorescens |
Zonisamide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Reductive metabolism |
n.a. |
PMID: 30227749
|
Escherichia coli |
Zonisamide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Reductive metabolism |
n.a. |
PMID: 30227749
|
Bacteroides vulgatus |
Zonisamide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Reductive metabolism |
n.a. |
PMID: 30227749
|
Enterococcus faecalis |
Zonisamide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Reductive metabolism |
n.a. |
PMID: 30227749
|
Clostridium sporogenes |
Zonisamide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Reductive metabolism |
n.a. |
PMID: 30227749
|
Bifidobacterium bifidum |
Zonisamide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Reductive metabolism |
n.a. |
PMID: 30227749
|
Lactobacillus rhamnosus |
Zonisamide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Reductive metabolism |
n.a. |
PMID: 30227749
|
Salmonella enterica subsp. enterica serovar Typhimurium |
Zonisamide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Reductive metabolism |
n.a. |
PMID: 30227749
|
Eubacterium sp. |
Balsalazide |
Therapeutic Substance |
Approved Drug |
n.a. |
5-aminosalicylic acid |
Increase Toxicity |
n.a. |
n.a. |
Reduction and Release of 5-aminosalicylic acid;Azoreductases |
Increase toxicity |
PMID: 30227749
|
Unidentified gut microbes |
Diclofenac |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Bacterial b-glucuronidases |
Reduce intestinal tract toxicity |
PMID: 30227749
|
Unidentified gut microbes |
Indomethacin |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Bacterial b-glucuronidases |
Reduce intestinal tract toxicity |
PMID: 30227749
|
Unidentified gut microbes |
Ketoprofen |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Bacterial b-glucuronidases |
Reduce intestinal tract toxicity |
PMID: 30227749
|
Eubacterium sp. |
Olsalazine |
Therapeutic Substance |
Approved Drug |
n.a. |
5-aminosalicylic acid |
Increase Toxicity |
n.a. |
n.a. |
Reduction and Release of 5-aminosalicylic acid;Azoreductases |
Increase toxicity |
PMID: 30227749
|
Eubacterium sp. |
Sulfasalazine |
Therapeutic Substance |
Approved Drug |
n.a. |
5-aminosalicylic acid |
Increase Toxicity |
n.a. |
n.a. |
Reduction and Release of 5-aminosalicylic acid;Azoreductases |
Increase toxicity |
PMID: 30227749
|
Unidentified gut microbes |
Mesalazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
N-acetyltransferase |
Acetylating to acid |
PMID: 11344150; PMID: 30338735
|
Unidentified gut microbes |
Nizatidine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Metabolized by bacteria |
n.a. |
PMID: 30338735; PMID: 11955801
|
Unidentified gut microbes |
Sulfonamide antibiotics |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Azoreductase enzymes |
Activation of prodrug to 5-aminosalicylic acid |
PMID: 30338735; PMID: 1711964
|
Clostridium perfringens |
Metronidazole |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Reduction to acetamide |
PMID: 30338735; PMID: 231450
|
Bacterium DZY-HS11 |
Arsenic |
Environmental Chemicals |
Toxic Agents |
n.a. |
n.a. |
n.a. |
Mouse |
n.a. |
Reduce the abundance of bacteria |
n.a. |
PMID: 30338735; PMID: 24413286
|
Unidentified gut microbes |
Lovastatin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Β-D-glucosidase, α-L-rhamnosidase,α-D-glucosidase enzyme |
Drug interaction:antibiotics can reduce the biotransformation |
PMID: 30338735; PMID: 24947972
|
Unidentified gut microbes |
Digitoxin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Β-glucuronidase |
Hydrolysis of glucuronide |
PMID: 28922; PMID: 30338735
|
Unidentified gut microbes |
Nifedipine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
Rat |
n.a. |
n.a. |
n.a. |
PMID: 30338735; PMID: 29790376
|
Unidentified gut microbes |
Nifedipine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
Hypoxic conditions at high altitudes |
Changes of intestinal microflora caused by high plateau hypoxia |
Increase the bioavailability of drug |
PMID: 30338735; PMID: 29790376
|
Unidentified gut microbes |
Metronidazole |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
Increase Toxicity |
n.a. |
n.a. |
n.a. |
Result in increased toxicity |
PMID: 30338735; PMID: 430360
|
Unidentified gut microbes |
Sulfasalazine |
Therapeutic Substance |
Approved Drug |
n.a. |
sulfapyridine and 5-ASA |
Decrease Efficacy |
n.a. |
n.a. |
n.a. |
Lose activity |
PMID: 30338735; PMID: 4402374
|
Unidentified gut microbes |
Sulfasalazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Active 5-aminosalicyclic acid by intestinal azoreductase enzymes |
Increase the drug |
PMID: 30338735; PMID: 4402374
|
Unidentified gut microbes |
Dihydroxyphenylalanine (DOPA) |
Therapeutic Substance |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Direct dopa to alternative metabolic pathways |
PMID: 4723308; PMID: 30338735
|
Unidentified gut microbes |
Artificial sweetener cyclamate |
Dietary Substance |
Dietary Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Hydrolysis |
n.a. |
PMID: 7362642; PMID: 30338735
|
Unidentified gut microbes |
Plant-derived glycosides(amygdalin) |
Herbal Substance |
Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Hydrolysis |
n.a. |
PMID: 7362642; PMID: 30338735
|
Unidentified gut microbes |
Loperamide oxide |
Therapeutic Substance |
Investigational Drug |
n.a. |
loperamide |
n.a. |
Human; Dog; Rat |
n.a. |
Bacteria affect activation of prodrugs and drug inactivation |
n.a. |
PMID: 30338735; PMID: 7628301
|
Unidentified gut microbes |
Nitrazepam |
Therapeutic Substance |
Approved Drug |
n.a. |
7-acetylaminonitrazepam |
n.a. |
n.a. |
n.a. |
Nitroreductase |
n.a. |
PMID: 30338735; PMID: 9310649
|
Clostridium |
Acetaminophen |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
p-cresol |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 30338735
|
Enterobacteriales |
Acetylsalicylic acid |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Drug interaction:antibiotics can potentiate the therapeutic potency |
PMID: 30338735
|
Enterococcus |
Acetylsalicylic acid |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Drug interaction:antibiotics can potentiate the therapeutic potency |
PMID: 30338735
|
Lactobacillus |
Acetylsalicylic acid |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Drug interaction:antibiotics can potentiate the therapeutic potency |
PMID: 30338735
|
Unidentified gut microbes |
Daidzein |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
calycosin |
n.a. |
n.a. |
n.a. |
Bacteria produces O-methyltransferase and aromatic hydroxylase |
n.a. |
PMID: 30338735
|
Eggerthella lenta |
Digoxin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
dihydrodigoxigenin,dihydrodigoxin |
Decrease Efficacy |
n.a. |
n.a. |
Reduction to inactive metabolites |
n.a. |
PMID: 30338735
|
Escherichia |
Diosmin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Generated to glycosidic bond, followed by diosmetin |
n.a. |
PMID: 30338735
|
Enterococcus |
Diosmin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Generated to glycosidic bond, followed by diosmetin |
n.a. |
PMID: 30338735
|
Clostridium |
Diosmin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Generated to glycosidic bond, followed by diosmetin |
n.a. |
PMID: 30338735
|
Lactobacillus |
Diosmin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Generated to glycosidic bond, followed by diosmetin |
n.a. |
PMID: 30338735
|
Bifidobacterium |
Diosmin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Generated to glycosidic bond, followed by diosmetin |
n.a. |
PMID: 30338735
|
Bacteroides |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
SN-38 |
n.a. |
n.a. |
n.a. |
Hydrolysis and release of SN-38 |
Leads to GI toxicity |
PMID: 30338735
|
Clostridium |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
SN-38 |
n.a. |
n.a. |
n.a. |
Hydrolysis and release of SN-38 |
Leads to GI toxicity |
PMID: 30338735
|
Escherichia coli |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
Increase Toxicity |
n.a. |
n.a. |
Β-glucuronidases |
Enhance the irinotecan toxicity |
PMID: 30338735
|
Bacteroides vulgatus |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
Increase Toxicity |
n.a. |
n.a. |
Β-glucuronidases |
Enhance the irinotecan toxicity |
PMID: 30338735
|
Erysipelatoclostridium ramosum |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
Increase Toxicity |
n.a. |
n.a. |
Β-glucuronidases |
Enhance the irinotecan toxicity |
PMID: 30338735
|
Bifidobacterium sp. |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
SN-38 |
n.a. |
n.a. |
n.a. |
Hydrolysis and release of SN-38 |
Leads to GI toxicity |
PMID: 30338735
|
Bacteroides |
Lactulose |
Therapeutic Substance |
Approved Drug |
n.a. |
acetic lactic,acids active |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 30338735
|
Clostridium |
Lactulose |
Therapeutic Substance |
Approved Drug |
n.a. |
acetic lactic,acids active |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 30338735
|
Lactobacillus |
Lactulose |
Therapeutic Substance |
Approved Drug |
n.a. |
acetic lactic,acids active |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 30338735
|
Bacteroides |
Levamisole |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
levametabol-I,levametabol-III |
Increase Efficacy |
n.a. |
n.a. |
n.a. |
Generate active metabolites |
PMID: 30338735
|
Clostridium sp. |
Levamisole |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
levametabol-I,levametabol-III |
Increase Efficacy |
n.a. |
n.a. |
n.a. |
Generate active metabolites |
PMID: 30338735
|
[Eubacterium] rectale |
Puerarin |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
daidzein |
n.a. |
n.a. |
n.a. |
Convert by bacteria |
n.a. |
PMID: 30338735
|
Bacteroides |
Rutin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Generated to glycosidic bond, followed by quercetin |
n.a. |
PMID: 30338735
|
Clostridium |
Rutin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Generated to glycosidic bond, followed by quercetin |
n.a. |
PMID: 30338735
|
Lactobacillus |
Rutin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Generated to glycosidic bond, followed by quercetin |
n.a. |
PMID: 30338735
|
Eubacterium |
Rutin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Generated to glycosidic bond, followed by quercetin |
n.a. |
PMID: 30338735
|
Bifidobacterium sp. |
Rutin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Generated to glycosidic bond, followed by quercetin |
n.a. |
PMID: 30338735
|
Escherichia |
Scutellaria baicalensis root |
Therapeutic Substance |
Investigational Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Generated to glycosidic bond,followed by baicalein. |
n.a. |
PMID: 30338735
|
Streptococcus |
Scutellaria baicalensis root |
Therapeutic Substance |
Investigational Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Generated to glycosidic bond,followed by baicalein. |
n.a. |
PMID: 30338735
|
Lactobacillus |
Scutellaria baicalensis root |
Therapeutic Substance |
Investigational Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Generated to glycosidic bond,followed by baicalein. |
n.a. |
PMID: 30338735
|
Eubacterium |
Scutellaria baicalensis root |
Therapeutic Substance |
Investigational Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Generated to glycosidic bond,followed by baicalein. |
n.a. |
PMID: 30338735
|
Bifidobacterium sp. |
Scutellaria baicalensis root |
Therapeutic Substance |
Investigational Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Generated to glycosidic bond,followed by baicalein. |
n.a. |
PMID: 30338735
|
Lactobacillus |
Simvastatin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
Increase Toxicity |
n.a. |
n.a. |
n.a. |
Increase the risk of myopathy |
PMID: 30338735
|
Bacteroides |
Sorivudine |
Therapeutic Substance |
Investigational Drug |
n.a. |
(E)-5-(2-bromovinyl) uracil |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 30338735
|
Gardnerella |
Tenofovir |
Therapeutic Substance |
Investigational Drug |
n.a. |
n.a. |
Decrease Efficacy |
n.a. |
n.a. |
Catabolized tenofovir into an inactive compound |
n.a. |
PMID: 30338735
|
Clostridium |
Zonisamide |
Therapeutic Substance |
Approved Drug |
n.a. |
2-sulphamoylacetylphenol |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 30338735
|
Unidentified gut microbes |
Daidzein |
Therapeutic Substance; Herbal Substance |
Investigational Drug; Medicinal Herbal Compounds |
n.a. |
Calycosin |
n.a. |
n.a. |
n.a. |
Aromatic hydroxylase,O-methyltransferase |
n.a. |
PMID: 30338735
|
Faecalibacterium prausnitzii |
Anti‑PD‑1 therapy |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
Human |
Patients with metastatic melanoma |
n.a. |
Higher relative abundance of bacteria in responding (R) patients;therapy is defined by eight species driven by Bifidobacterium longum |
PMID: 30530851
|
Bifidobacterium longum |
Anti‑PD‑1 therapy |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
Human |
Patients with metastatic melanoma |
n.a. |
Higher relative abundance of bacteria in responding (R) patients;therapy is defined by eight species driven by Bifidobacterium longum |
PMID: 30530851
|
Akkermansia muciniphila |
Anti‑PD‑1 therapy |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
Human |
Patients with non-small cell lung cancer |
n.a. |
Increased relative abundance of bacteria in PD-1 R |
PMID: 30530851
|
Unidentified gut microbes |
Simvastatin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
Increase Efficacy |
Human |
n.a. |
n.a. |
221% increase in simvastatin AUC for homozygotes |
PMID: 19833260; PMID: 18650507; PMID: 24918167; PMID: 22380001; PMID: 31171383
|
Eggerthella lenta |
Digoxin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
Lactone ring reduction |
n.a. |
Increase Toxicity |
Human |
n.a. |
n.a. |
Decreased AUC; narrow therapeutic window |
PMID: 24637603; PMID: 18334914; PMID: 31171383
|
Unidentified gut microbes |
Warfarin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
Human |
n.a. |
Vitamin K production |
Altered activity of drug |
PMID: 22380001; PMID: 17042764; PMID: 26962786; PMID: 31171383
|
Unidentified gut microbes |
Bromazepam |
Therapeutic Substance |
Approved Drug |
Nitroreduction |
n.a. |
Increase Toxicity |
Human |
n.a. |
n.a. |
Amino-metabolite generation, Inactivation |
PMID: 27591027; PMID: 30227749; PMID: 31171383
|
Unidentified gut microbes |
Bromazepam |
Therapeutic Substance |
Approved Drug |
Nitroreduction |
n.a. |
Decrease Efficacy |
Human |
n.a. |
n.a. |
Change to inactive metabolite |
PMID: 27591027; PMID: 30227749; PMID: 31171383
|
Unidentified gut microbes |
Clonazepam |
Therapeutic Substance |
Approved Drug |
Nitroreduction |
n.a. |
Increase Toxicity |
Human |
n.a. |
n.a. |
Amino-metabolite generation, Inactivation |
PMID: 27591027; PMID: 30227749; PMID: 31171383
|
Unidentified gut microbes |
Clonazepam |
Therapeutic Substance |
Approved Drug |
Nitroreduction |
n.a. |
Decrease Efficacy |
Human |
n.a. |
n.a. |
Change to inactive metabolite |
PMID: 27591027; PMID: 30227749; PMID: 31171383
|
Unidentified gut microbes |
Diclofenac |
Therapeutic Substance |
Approved Drug |
Deglucuronidation |
n.a. |
Increase Toxicity |
Human |
n.a. |
n.a. |
Reformation of cytotoxic drug;Diarrhea, bowel distress, GI lesions |
PMID: 27591027; PMID: 30227749; PMID: 31171383
|
Unidentified gut microbes |
Indomethacin |
Therapeutic Substance |
Approved Drug |
Deglucuronidation |
n.a. |
Increase Toxicity |
Human |
n.a. |
n.a. |
Reformation of cytotoxic drug;Diarrhea, bowel distress, GI lesions |
PMID: 27591027; PMID: 30227749; PMID: 31171383
|
Unidentified gut microbes |
Irinotecan |
Therapeutic Substance |
Approved Drug |
Deglucuronidation |
n.a. |
Increase Toxicity |
Human |
n.a. |
n.a. |
Reformation of cytotoxic drug;Diarrhea, bowel distress, GI lesions |
PMID: 27591027; PMID: 30227749; PMID: 31171383
|
Unidentified gut microbes |
Ketoprofen |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
Deglucuronidation |
n.a. |
Increase Toxicity |
Human |
n.a. |
n.a. |
Reformation of cytotoxic drug;Diarrhea, bowel distress, GI lesions |
PMID: 27591027; PMID: 30227749; PMID: 31171383
|
Unidentified gut microbes |
Nitrazepam |
Therapeutic Substance |
Approved Drug |
Nitroreduction |
n.a. |
Increase Toxicity |
Human |
n.a. |
n.a. |
Amino-metabolite generation, Inactivation |
PMID: 27591027; PMID: 30227749; PMID: 31171383
|
Unidentified gut microbes |
Nitrazepam |
Therapeutic Substance |
Approved Drug |
Nitroreduction |
n.a. |
Decrease Efficacy |
Human |
n.a. |
n.a. |
Change to inactive metabolite |
PMID: 27591027; PMID: 30227749; PMID: 31171383
|
Unidentified gut microbes |
Irinotecan |
Therapeutic Substance |
Approved Drug |
Deglucuronidation |
SN-38G metabolite |
Increase Toxicity |
Human |
n.a. |
n.a. |
Defect in glucuronidation; increased toxicity |
PMID: 29104759; PMID: 18349289; PMID: 31171383
|
Unidentified gut microbes |
Acetaminophen |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
Sulfonation |
n.a. |
Decrease Toxicity |
Human |
n.a. |
n.a. |
Increased rate of glucuronidation; decreased risk of liver failure |
PMID: 23408116; PMID: 19667173; PMID: 29705271; PMID: 31171383
|
Unidentified gut microbes |
Brivudine |
Therapeutic Substance |
Approved Drug |
n.a. |
additional bromovinyluracil |
Increase Toxicity |
Human |
n.a. |
n.a. |
Hepatotoxicity; bromovinyluracil prevents clearance of 5-FU |
PMID: 9690942; PMID: 30733391; PMID: 31171383
|
Unidentified gut microbes |
Sorivudine |
Therapeutic Substance |
Investigational Drug |
n.a. |
additional bromovinyluracil |
Increase Toxicity |
Human |
n.a. |
n.a. |
Hepatotoxicity; bromovinyluracil prevents clearance of 5-FU |
PMID: 9690942; PMID: 30733391; PMID: 31171383
|
Unidentified gut microbes |
Balsalazide |
Therapeutic Substance |
Approved Drug |
Azoreduction |
local 5-ASA |
Increase Efficacy |
Human |
n.a. |
n.a. |
Prodrug activation: local 5-ASA release |
PMID: 27591027; PMID: 31171383
|
Unidentified gut microbes |
Calcitonin |
Therapeutic Substance |
Approved Drug |
Proteolysis |
n.a. |
Decrease Efficacy |
Human |
n.a. |
n.a. |
Breakdown of therapeutic protein |
PMID: 27591027; PMID: 31171383
|
Unidentified gut microbes |
Chloramphenicol |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
Nitroreduction |
p-aminophenyl-2-amino-1,3-propanediol |
Increase Toxicity |
Human |
n.a. |
n.a. |
Bone marrow toxicity |
PMID: 27591027; PMID: 31171383
|
Unidentified gut microbes |
Insulin human |
Therapeutic Substance |
Approved Drug |
Proteolysis |
n.a. |
Decrease Efficacy |
Human |
n.a. |
n.a. |
Breakdown of therapeutic protein |
PMID: 27591027; PMID: 31171383
|
Unidentified gut microbes |
Ipsalazide |
Therapeutic Substance |
Approved Drug |
Azoreduction |
local 5-ASA |
Increase Efficacy |
Human |
n.a. |
n.a. |
Prodrug activation: local 5-ASA release |
PMID: 27591027; PMID: 31171383
|
Unidentified gut microbes |
Neoprontosil |
Therapeutic Substance |
Approved Drug |
Azoreduction |
n.a. |
Increase Efficacy |
Human |
n.a. |
n.a. |
Antibiotic activation |
PMID: 27591027; PMID: 31171383
|
Unidentified gut microbes |
Olsalazine |
Therapeutic Substance |
Approved Drug |
Azoreduction |
local 5-ASA |
Increase Efficacy |
Human |
n.a. |
n.a. |
Prodrug activation: local 5-ASA release |
PMID: 27591027; PMID: 31171383
|
Unidentified gut microbes |
Picosulfuric acid |
Therapeutic Substance |
Approved Drug |
Desulfation |
n.a. |
Increase Efficacy |
Human |
n.a. |
n.a. |
Solubility increase |
PMID: 27591027; PMID: 31171383
|
Unidentified gut microbes |
Prontosil |
Therapeutic Substance |
Approved Drug |
Azoreduction |
n.a. |
Increase Efficacy |
Human |
n.a. |
n.a. |
Antibiotic activation |
PMID: 27591027; PMID: 31171383
|
Unidentified gut microbes |
Sulfadiazine |
Therapeutic Substance |
Approved Drug |
Azoreduction |
local 5-ASA |
Increase Efficacy |
Human |
n.a. |
n.a. |
Prodrug activation: local 5-ASA release |
PMID: 27591027; PMID: 31171383
|
Unidentified gut microbes |
Mesalazine |
Therapeutic Substance |
Approved Drug |
N-Acetylation |
n.a. |
Decrease Efficacy |
Human |
n.a. |
n.a. |
Less efficacy; possible pancreatic toxicity |
PMID: 30227749; PMID: 31171383
|
Unidentified gut microbes |
Amiodarone |
Therapeutic Substance |
Approved Drug |
N-dealkylation |
n.a. |
Increase Efficacy |
Human |
n.a. |
n.a. |
Increased bioavailability of active metabolite |
PMID: 30227749; PMID: 31171383
|
Unidentified gut microbes |
Codeine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
Deglucuronidation |
n.a. |
Increase Efficacy |
Human |
n.a. |
n.a. |
Reformation of active metabolite |
PMID: 30227749; PMID: 31171383
|
Unidentified gut microbes |
Digoxin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
Lactone ring reduction |
n.a. |
Decrease Efficacy |
Human |
n.a. |
n.a. |
Change to inactive metabolite |
PMID: 30227749; PMID: 31171383
|
Unidentified gut microbes |
Metamfetamine |
Therapeutic Substance |
Approved Drug |
N-Demethylation |
n.a. |
Decrease Efficacy |
Human |
n.a. |
n.a. |
Change to inactive metabolite |
PMID: 30227749; PMID: 31171383
|
Unidentified gut microbes |
Morphine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
Deglucuronidation |
n.a. |
Increase Efficacy |
Human |
n.a. |
n.a. |
Reformation of active metabolite |
PMID: 30227749; PMID: 31171383
|
Unidentified gut microbes |
Brivudine |
Therapeutic Substance |
Approved Drug |
N-Dealkylation |
n.a. |
Increase Toxicity |
Human |
n.a. |
n.a. |
Bacteroides-mediated hepatotoxicity; potentially fatal 5-FU accumulation |
PMID: 30733391; PMID: 31171383
|
Unidentified gut microbes |
Sorivudine |
Therapeutic Substance |
Investigational Drug |
N-Dealkylation |
n.a. |
Increase Toxicity |
Human |
n.a. |
n.a. |
Bacteroides-mediated hepatotoxicity; potentially fatal 5-FU accumulation |
PMID: 30733391; PMID: 31171383
|
Helicobacter pylori |
Levodopa |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
P-Dehydroxylation |
n.a. |
Decrease Efficacy |
Human |
n.a. |
n.a. |
Decrease in L-dopa absorption |
PMID: 31171383
|
Pseudomonas aeruginosa |
Morphine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
Deglucuronidation |
morphine-glucuronide metabolite |
n.a. |
Human |
n.a. |
n.a. |
Decreased clearance of morphine; Induces virulence in some strains of Pseudomonas aeruginosa |
PMID: 31171383
|
Unidentified gut microbes |
Estradiol |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
Increase Bioavailability |
human |
n.a. |
Β-glucuronidase mediate deconjugation and enterohepatic circulation of estrogen |
Greater absroption of estrogens;develop estrogen-driven cancer |
PMID: 27107051; PMID: 31184303; PMID: 24187630
|
Unidentified gut microbes |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
Increase Toxicity |
Human; Mouse |
n.a. |
Microbial β-glucuronidases mediate the reactivation of metabolite(deconjugation and reactivation of SN-38) |
Cause toxicity(epithelial damage;severe diarrhea);analog:plant-based compound scutellarin(inadvertently modulating the effect of cancer therapy) |
PMID: 29104759; PMID: 21051639; PMID: 31184303
|
Unidentified gut microbes |
Taurine conjugated bile acid |
Environmental Chemicals |
Human Metabolite |
n.a. |
n.a. |
Increase Toxicity |
n.a. |
n.a. |
Meidate de-conjugation of taurineconjugates;generate hydrogen sulfid |
Contribute to the etiology of cancer |
PMID: 27003186; PMID: 31184303
|
Eggerthella lenta |
Digoxin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
Decrease Efficacy |
human |
n.a. |
Be linked to cgr operon expression levels;human microbiome reductase inactivates the drug |
Lead to inactivation and decreased bioavailability;drug substructure similarity:cardenolides(great),progesterone、cortisone(bad); |
PMID: 31184303
|
Unidentified gut microbes |
Altretamine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
Increase Toxicity |
Human |
n.a. |
Alter the drug structure |
Cause diarrhea and kidney damage;interaction:tamoxifen、diphenhydramine、theobromine |
PMID: 31184303
|
Pseudomonas putida |
Altretamine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
Increase Toxicity |
n.a. |
n.a. |
Microbial N-demethylase enzymes |
Lead to similar toxic effects as seen with melamine;Substrate similar(no evidence) |
PMID: 31184303
|
Styrax aureus |
Hypochlorite |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Human |
Patients with cutaneous T cell lymphoma |
n.a. |
Reduce the amount of bacteria |
PMID: 18835065; PMID: 31186074
|
Unidentified probiotic |
Common azole treatment |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Reduce the amount of azoleresistant fungal strains |
PMID: 25362524; PMID: 31186074
|
Unidentified gut microbes |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Reactivate drug by the β-glucuronidase enzyme |
Result in side effects( stage 4 diarrhea and gastrointestinal damage) |
PMID: 31186074; PMID: 26364932
|
Unidentified gut microbes |
Levodopa |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
m-tyramine, m-hydroxyphenylacetic acid (m-HPAA) |
Decrease Efficacy |
Rat |
n.a. |
n.a. |
Decrease L-DOPA half-life and efficacy |
PMID: 4723308; PMID: 31186074
|
Unidentified gut microbes |
Lactulose |
Therapeutic Substance |
Approved Drug |
n.a. |
acetic,lactic acid |
Increase Efficacy |
n.a. |
n.a. |
n.a. |
Product therapeutic metabolites |
PMID: 6804597; PMID: 31186074
|
Unidentified gut microbes |
Antibiotic (extensive treatment) |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Eliminate the majority of the intestinal microbiome and improve harmful bacteria(Clostridium difficile) |
Lead to intestinal complications(antibiotic-associated diarrhea and colitis);drug interaction: C. difficile can be treated with vancomycin and metronidazole |
PMID: 31186074
|
Unidentified gut microbes |
Bromazepam |
Therapeutic Substance |
Approved Drug |
n.a. |
7-aminoclonazepam,2-(2-amino-5-bromobenzoyl) pyridine |
n.a. |
n.a. |
n.a. |
Gut microbial nitroreductase activity |
n.a. |
PMID: 2893665; PMID: 6506755
|
Unidentified gut microbes |
Clonazepam |
Therapeutic Substance |
Approved Drug |
n.a. |
7-aminoclonazepam,2-(2-amino-5-bromobenzoyl) pyridine |
n.a. |
n.a. |
n.a. |
Gut microbial nitroreductase activity |
n.a. |
PMID: 2893665; PMID: 6506755
|
Unidentified gut microbes |
Potassium oxonate |
Environmental Chemicals |
Unclassified Substance |
n.a. |
cyanuric acid |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
PMID: 10997934
|
Unidentified gut microbes |
Sulfasalazine |
Therapeutic Substance |
Approved Drug |
n.a. |
N-acetyl sulfapyridine,N-acetyl-5-aminosalicylic acid |
n.a. |
Human; Rat; Guinea pig; Dog |
n.a. |
Bacterial N-acetylation |
n.a. |
PMID: 1425876
|
Unidentified gut microbes |
Picosulfuric acid |
Therapeutic Substance |
Approved Drug |
n.a. |
4,40-dihydroxydiphenyl-(2 pyridyl)-methane |
n.a. |
n.a. |
n.a. |
Conversion by gut bacteria |
n.a. |
PMID: 1507649
|
Unidentified gut microbes |
Phosphate or sulfate ester prodrugs |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
The drug act on hydrolytic enzymes of bacteria |
n.a. |
PMID: 1507649
|
Unidentified gut microbes |
Sulfasalazine |
Therapeutic Substance |
Approved Drug |
n.a. |
5-amino 5-salicylic acid |
Increase Efficacy |
n.a. |
n.a. |
Microbial azoreductases |
Convert to its pharmacologically active form;enhance drug distribution:olsalazine、balsalazide(inflammatory bowel disease)——introduction of azo bonds |
PMID: 18305431
|
Unidentified gut microbes |
Antibiotic |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Eliminate vitamin K-producing bacteria |
Lead to alteration in coagulation status |
PMID: 18841274
|
Unidentified gut microbes |
Nitrazepam |
Therapeutic Substance |
Approved Drug |
n.a. |
7-aminonitrazepam,7-acetylaminonitrazepam |
Increase Toxicity |
Rat |
Pregnant |
Gut microbial nitroreductase activity |
Lead to nitrazepam-related teratogenicity;drug interaction:antibiotic reduced metabolites |
PMID: 1925980
|
Unidentified gut microbes |
Acetaminophen |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
N-acetyl p-benzoquuinone imine |
Increase Toxicity |
Human |
n.a. |
A microbial-derived metabolite p-cresol compete with acetaminophen |
Impede the ability for the liver to detoxify |
PMID: 19667173; PMID: 31462078
|
Unidentified anaerobic bacterium |
Fostamatinib |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Microbial O-dealkylation |
n.a. |
PMID: 20371637
|
Unidentified gut microbes |
Rosuvastatin |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
Increase Toxicity |
n.a. |
n.a. |
Compete with TMA for metabolism by FMO3 |
Cause side effect on fish odor syndrom |
PMID: 21422137
|
Unidentified gut microbes |
Indomethacin |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Mouse |
n.a. |
n.a. |
Alterations in bacteria(expansion of proinflammatory bacteria) |
PMID: 22328575
|
Unidentified gut microbes |
Metronidazole |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
1-(2-aminoimidazol-1-yl)-3 methoxypropanol-2-ol and acetamide |
n.a. |
Rat |
n.a. |
Gut microbiome–derived nitroreduction |
Lead to rat carcinogen |
PMID: 231450
|
Unidentified gut microbes |
Digoxin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
Decrease Efficacy |
n.a. |
n.a. |
n.a. |
Microbial inactivation |
PMID: 23869020
|
Unidentified gut microbes |
CpG-oligonucleotide immunotherapy |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Prime murine immune cells to secrete tumor necrosis factor(TNF) |
Stimulate the immune system to attack cancer cells |
PMID: 24264989
|
Unidentified gut microbes |
Lovastatin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Drug interaction:long-term antibiotic treatment might lead to a failure to control serum cholesterol levels |
PMID: 24947972
|
Unidentified gut microbes |
Sulfasalazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
Increase Efficacy |
n.a. |
n.a. |
n.a. |
Lead to activation of drug |
PMID: 25091594
|
Unidentified gut microbes |
Eltrombopag |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Human; Dog |
n.a. |
Reductive cleavag |
n.a. |
PMID: 25581726
|
Unidentified gut microbes |
Levosimendan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Human; Dog |
n.a. |
Reductive cleavag |
n.a. |
PMID: 25581726
|
Unidentified gut microbes |
Indole |
Therapeutic Substance; Herbal Substance |
Investigational Drug |
n.a. |
indole-3-propionic acid |
n.a. |
n.a. |
n.a. |
n.a. |
Provide ligands for the aryl hydrocarbon receptor |
PMID: 26041783
|
Unidentified gut microbes |
Tryptophan |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
indole-3-propionic acid |
n.a. |
n.a. |
n.a. |
n.a. |
Provide ligands for the aryl hydrocarbon receptor |
PMID: 26041783
|
Unidentified gut microbes |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
B-glucuronidase activity |
Lead to severe diarrhea;drug interaction:antibiotic mixtures(streptomycin,penicillin or neomycin and bacitracin)eliminated fecal b-glucuronidase activity; TJ-14 administration moderate weight loss and delay the drug-associated diarrhea; the P-glycoprotein and (cMOA T/MRP2) inhibitor of cyclosporin A or (UDP)-glucuronosyltransferase inhibitor valproic acid increased intestinal toxicity |
PMID: 26518357
|
Unidentified gut microbes |
Indomethacin |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
Increase Efficacy |
Mouse |
n.a. |
Β-glucuronidases |
Enhance pharmacological effect |
PMID: 26701907
|
Unidentified oral microbes |
PPIs |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Associated with changes toward a less healthy gut microbiome and in line with changes predisposing users to infection with C. difficile |
Species of bacteria were seen to be over-represented in the fecal microbiome |
PMID: 26719299
|
Unidentified gut microbes |
PPIs |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Changes in bacterial populations(decrease Bacteroidetes and increase Firmicutes) |
Predispose PPI-treated subjects to C. difficile infection;[drug interaction]:frequent use of PPIs can exacerbate NSAID-induced small intestinal injury;[probiotics]prevent NSAID-induced damage in patients receiving PPI and NSAIDs |
PMID: 26923470
|
Unidentified gut microbes |
Rosuvastatin |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Mouse |
With rosuvastatin |
Reduce hepatic expression of the CYP27a1,alter the concentrations of bile acids |
Contribute to the composition of gut microbiota |
PMID: 28209601
|
Unidentified gut microbes |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
Decrease Toxicity |
n.a. |
n.a. |
n.a. |
Causes toxic side effects |
PMID: 29104759
|
Unidentified gut microbes |
Levodopa |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
dopamine |
n.a. |
n.a. |
n.a. |
Tyrosine decarboxylase |
n.a. |
PMID: 30659181
|
Escherichia coli |
Flucytosine |
Therapeutic Substance |
Approved Drug |
n.a. |
5-FU |
n.a. |
n.a. |
n.a. |
Deamination by bacteria |
n.a. |
PMID: 3729334
|
Unidentified gut microbes |
2-amino-3,6-dihydro-3H-imidazo[4,5-f]quinoline |
Environmental Chemicals |
Unclassified Substance |
n.a. |
7-hydroxy metabolite |
n.a. |
n.a. |
n.a. |
Gut microbiotal oxidation/dehydrogenation |
n.a. |
PMID: 3821779
|
Unidentified gut microbes |
Acetaminophen |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Drug is deacetylated |
n.a. |
PMID: 4418213
|
Unidentified gut microbes |
Phenacetin |
Therapeutic Substance |
Approved Drug (Withdrawn) |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Drug is deacetylated |
n.a. |
PMID: 4418213
|
Unidentified gut microbes |
Levodopa |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
m-hydroxyphenylacetic acid |
n.a. |
Rat |
n.a. |
Some microbial dehydroxylation |
Reduce the exposure of the drug in the brain |
PMID: 5343357
|
Unidentified gut microbes |
Methotrexate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Mouse |
Normal |
n.a. |
n.a. |
PMID: 5345205
|
Unidentified gut microbes |
Radiation sensitizer misonidazole |
Therapeutic Substance |
n.a. |
n.a. |
l-(2-l-(2-aminoimidazol-l-yl)-3-methoxypropan-2-ol |
n.a. |
Rat |
Normal,germ-free(GF) |
Nitroreduction |
Drug interaction:penicillin increased drug exposure and decreased neurotoxicity |
PMID: 6260109
|
Unidentified gut microbes |
Risperidone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Rat; Dog |
n.a. |
Reductive metabolism |
n.a. |
PMID: 7512019
|
Unidentified gut microbes |
Calcitonin |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Rat |
n.a. |
n.a. |
Drug is rapidly degraded;more prone to proteolysis;drug interaction:protease inhibitors(camostat/aprotinin) improve the stability and bioavailability of these peptides |
PMID: 7550138
|
Unidentified gut microbes |
Loperamide oxide |
Therapeutic Substance |
Investigational Drug |
n.a. |
loperamide,the ranitidine,nitazidine |
n.a. |
Dog |
n.a. |
n.a. |
n.a. |
PMID: 7628301
|
Unidentified gut microbes |
Omeprazole |
Therapeutic Substance |
Approved Drug |
n.a. |
sulfide metabolite |
n.a. |
n.a. |
n.a. |
Reduction |
n.a. |
PMID: 7629748
|
Unidentified anaerobic bacterium |
Azetirelin |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Rat |
n.a. |
n.a. |
Drug interaction:concentrations of the drug were maintained after the administration of antibiotic |
PMID: 9279880
|
Bacteroides |
1-b-D-arabinofuranosyl-5-(E)-(2-bromovinyl)uracil |
Environmental Chemicals |
Unclassified Substance |
n.a. |
BVU |
n.a. |
Rat |
n.a. |
The result of hydrolysis by anaerobic bacteria |
Drug interaction: the drug with the anticancer drug 5-FU or prodrugs tegafur,5-FU accumulate(increase toxicity, including death) |
PMID: 9808711
|
Unidentified gut microbes |
Sulfanilamide |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
molecule sulfanilamide |
Increase Efficacy |
n.a. |
n.a. |
n.a. |
Generate the active form of the drug |
PMID: 31235939
|
Bacteroides thetaiotaomicron |
Diltiazem |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Mouse |
Germ-free(GF) |
Bt4096 encodes an enzyme that metabolizes diltiazem |
n.a. |
PMID: 31235939
|
Faecalibacterium |
Anti‑PD‑1 therapy |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
n.a. |
Human |
Patients with melanoma |
n.a. |
Prolong progession-free survival |
PMID: 31462078
|
Bacteroidetes |
Checkpoint inhibitor therapy |
Therapeutic Substance |
Drug Class |
n.a. |
n.a. |
Decrease Toxicity |
n.a. |
n.a. |
Overabundance of the bacteroidetes phylum |
Decrease occrrence of side effect |
PMID: 31462078
|
Eggerthella lenta |
Digoxin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
dihydrodigoxin |
Decrease Bioavailability |
Human |
n.a. |
A cytochrome-encoding operon (termed the cardiac glycoside reductase) |
Convert to the inactive microbial metabolite;limit absorbtion;drug interaction:antibiotics,arginine-rich diet(impair this reaction) |
PMID: 31462078
|
Unidentified gut microbes |
Rosuvastatin |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Human |
Patients with with hyperlipidemia |
Activity of bacteria containing bile salt hydrolases |
Phyla Firmicutes、Fusobacteria(negatively associated with LDL-C levels);Cyanobacteria、Lentisphaerae(positively) |
PMID: 31462078
|
Firmicutes |
Rosuvastatin |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Human |
n.a. |
Bile salt hydrolase activity |
Reduce LDL-C levels |
PMID: 31462078
|
Lactobacillus reuteri |
Rosuvastatin |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Human |
n.a. |
Bile salt hydrolase activity |
Reduce LDL-C levels |
PMID: 31462078
|
Unidentified gut microbes |
Irinotecan |
Therapeutic Substance |
Approved Drug |
n.a. |
SN-38 |
Increase Toxicity |
n.a. |
n.a. |
Β-glucuronidases remove the glucuronide group;reactive the drug |
Sever diarrhea;drug interaction(mice:oral administration of a specific inhibitor of the β-glucuronidase enzyme,reduce irinotecan-induced toxicity) |
PMID: 31462078
|
Unidentified gut microbes |
Dietary choline |
Dietary Substance |
Dietary Compounds |
n.a. |
trimethylamine-N-oxide(TMAO) |
Increase Toxicity |
n.a. |
n.a. |
Microbiome-derived metabolites |
Interfer with drug pharmacokinetics and pharmacodynamics |
PMID: 31462078
|
Unidentified gut microbes |
Levocarnitine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
trimethylamine-N-oxide(TMAO) |
Increase Toxicity |
n.a. |
n.a. |
Microbiome-derived metabolites |
Interfer with drug pharmacokinetics and pharmacodynamics |
PMID: 31462078
|
Unidentified gut microbes |
Acetylsalicylic acid |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
n.a. |
Damage the mucosa of the upper GI tract;be able to distinguish aspirin users:(Prevotella species, Bacteroides species, a member of the Ruminococaceae family, and Barnesiella species |
PMID: 31462078
|
Unidentified gut microbes |
Amlodipine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Human; Rat |
n.a. |
Presystemic metabolism by dehydrogenation |
Decreased amount of active drug reaching target tissues;its major metabolite increased;drug interaction:rat(pretreated with ampicillin),enhance amlodipine's absorption; |
PMID: 31462078
|
Unidentified gut microbes |
Atorvastatin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
Human; Rat |
Rat(high-fat diet);hypercholesterolemia patients |
Decreased amount of secondary bile acids |
Increase abundance of putative anti-inflammatory species |
PMID: 31462078
|
Unidentified gut microbes |
Captopril |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
Rat |
Hypertensive |
Decreased intestinal permeability and fibrosis; and improved villi length |
Reverse the dysbiotic state |
PMID: 31462078
|
Unidentified gut microbes |
Clonazepam |
Therapeutic Substance |
Approved Drug |
n.a. |
7-aminoclonazapam |
n.a. |
n.a. |
n.a. |
Reduction reactions |
Drug interaction:antibiotics(inhibit) |
PMID: 31462078
|
Unidentified gut microbes |
Simvastatin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
Decrease Efficacy |
n.a. |
n.a. |
Microbial-derived bile acids competing for host uptake transporters |
Decreased amount of drug reaching target tissues |
PMID: 31462078
|
Unidentified gut microbes |
Simvastatin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
Human |
n.a. |
Bacterial-derived bile acids(lithocholic acid,taurolithocholic acid,glycolithocholic acid) |
Predict the magnitude of LDL-C lowering |
PMID: 31462078
|
Unidentified gut microbes |
Nitrazepam |
Therapeutic Substance |
Approved Drug |
n.a. |
7-amino-nitrazepam |
Increase Toxicity |
n.a. |
n.a. |
Nitro reduction by microbiota |
Produce a teratogenic metabolite;drug interaction:antibiotics(inhibit) |
PMID: 31462078
|
Bacteroides dorei DSM17855 |
Alfuzosin |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.339 [FDR-adjusted p-Value=0.006] |
PMID: 31158845
|
Bifidobacterium ruminatum |
Alprenolol |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.339 [FDR-adjusted p-Value=0.007] |
PMID: 31158845
|
Bifidobacterium breve DSM20213 |
Benzbromarone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.828 [FDR-adjusted p-Value=0.049] |
PMID: 31158845
|
Clostridium difficile 120 |
Camylofine dihydrochloride |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.425 [FDR-adjusted p-Value=0.05] |
PMID: 31158845
|
Salmonella typhimurium LT2 |
Capecitabine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-3.688 [FDR-adjusted p-Value=0.014] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Clemizole |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.408 [FDR-adjusted p-Value=0.047] |
PMID: 31158845
|
Bifidobacterium ruminatum |
Diphenylpyraline |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.329 [FDR-adjusted p-Value=0.014] |
PMID: 31158845
|
Eubacterium rectale ATCC33656 |
Ethoxzolamide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.557 [FDR-adjusted p-Value=0.016] |
PMID: 31158845
|
Bifidobacterium ruminatum |
Irsogladine maleate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.45 [FDR-adjusted p-Value=0.016] |
PMID: 31158845
|
Bacteroides fragilis ATCC43859 |
Lofexidine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.341 [FDR-adjusted p-Value=0.041] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Metitepine maleate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.765 [FDR-adjusted p-Value=0.021] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Orphenadrine citrate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.408 [FDR-adjusted p-Value=0.026] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Oxcarbazepine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.441 [FDR-adjusted p-Value=0.048] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Papaverine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.394 [FDR-adjusted p-Value=0.008] |
PMID: 31158845
|
Clostridium sp. |
Paroxetine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.378 [FDR-adjusted p-Value=0.041] |
PMID: 31158845
|
Bacteroides coprophilus DSM18228 |
Rizatriptan benzoate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.54 [FDR-adjusted p-Value=0.025] |
PMID: 31158845
|
Bacteroides fragilis HMW610 |
Sulpiride |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.399 [FDR-adjusted p-Value=0.04] |
PMID: 31158845
|
Bacteroides fragilis 3397 T10 |
Trimetazidine dihydrochloride |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.72 [FDR-adjusted p-Value=0.013] |
PMID: 31158845
|
Bacteroides vulgatus ATCC8482 |
Verapamil |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.372 [FDR-adjusted p-Value=0.03] |
PMID: 31158845
|
Anaerococcus hydrogenalis DSM7454 |
Zidovudine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.952 [FDR-adjusted p-Value=0.047] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Acecainide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.376 [FDR-adjusted p-Value=0.009] |
PMID: 31158845
|
Bacteroides fragilis ATCC43859 |
Acecainide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.345 [FDR-adjusted p-Value=0.031] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Anastrozole |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.381 [FDR-adjusted p-Value=0.003] |
PMID: 31158845
|
Clostridium sp. |
Anastrozole |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.443 [FDR-adjusted p-Value=0.017] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Benzthiazide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.459 [FDR-adjusted p-Value=0.045] |
PMID: 31158845
|
Clostridium sp. |
Benzthiazide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.459 [FDR-adjusted p-Value=0.002] |
PMID: 31158845
|
Bacteroides fragilis HMW610 |
Bicalutamide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.612 [FDR-adjusted p-Value=0.003] |
PMID: 31158845
|
Bacteroides fragilis HMW615 |
Bicalutamide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.493 [FDR-adjusted p-Value=0.038] |
PMID: 31158845
|
Escherichia coli BW25113 |
Bupropion |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.598 [FDR-adjusted p-Value=0.011] |
PMID: 31158845
|
Bifidobacterium ruminatum |
Bupropion |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.682 [FDR-adjusted p-Value=0.035] |
PMID: 31158845
|
Clostridium sporogenes ATCC15579 |
Celecoxib |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.809 [FDR-adjusted p-Value=0.031] |
PMID: 31158845
|
Eubacterium biforme DSM3989 |
Celecoxib |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.898 [FDR-adjusted p-Value=0.014] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Cyclobenzaprine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.482 [FDR-adjusted p-Value=0.035] |
PMID: 31158845
|
Clostridium sp. |
Cyclobenzaprine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.449 [FDR-adjusted p-Value=0.013] |
PMID: 31158845
|
Bacteroides vulgatus ATCC8482 |
Imatinib |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.453 [FDR-adjusted p-Value=0.028] |
PMID: 31158845
|
Anaerostipes sp. |
Imatinib |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.405 [FDR-adjusted p-Value=0.037] |
PMID: 31158845
|
Bifidobacterium ruminatum |
Memantine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.419 [FDR-adjusted p-Value=0.047] |
PMID: 31158845
|
Eubacterium biforme DSM3989 |
Memantine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.329 [FDR-adjusted p-Value=0.046] |
PMID: 31158845
|
Clostridium sp. |
Methsuximide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.51 [FDR-adjusted p-Value=0.035] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Methsuximide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.348 [FDR-adjusted p-Value=0.034] |
PMID: 31158845
|
Dorea formicigenerans ATCC27755 |
Methysergide maleate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.374 [FDR-adjusted p-Value=0.014] |
PMID: 31158845
|
Victivallis vadensis ATCC BAA-548 |
Methysergide maleate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.348 [FDR-adjusted p-Value=0.034] |
PMID: 31158845
|
Bifidobacterium ruminatum |
Metoprolol tartrate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.347 [FDR-adjusted p-Value=0.023] |
PMID: 31158845
|
Bacteroides fragilis ATCC43859 |
Metoprolol tartrate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.328 [FDR-adjusted p-Value=0.039] |
PMID: 31158845
|
Akkermansia muciniphila ATCC BAA-835 |
Naftopidil |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.325 [FDR-adjusted p-Value=0.022] |
PMID: 31158845
|
Bacteroides fragilis HMW610 |
Naftopidil |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-4.006 [FDR-adjusted p-Value=0.004] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Nevirapine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.441 [FDR-adjusted p-Value=0.006] |
PMID: 31158845
|
Clostridium sp. |
Nevirapine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.474 [FDR-adjusted p-Value=0.008] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Thiothixene |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.577 [FDR-adjusted p-Value=0.043] |
PMID: 31158845
|
Clostridium sp. |
Thiothixene |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.594 [FDR-adjusted p-Value=0.003] |
PMID: 31158845
|
Bacteroides thetaiotaomicron 3731 |
Tranilast |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.45 [FDR-adjusted p-Value=0.023] |
PMID: 31158845
|
Bacteroides fragilis HMW610 |
Tranilast |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.56 [FDR-adjusted p-Value=0.033] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Vinpocetine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.442 [FDR-adjusted p-Value=0.018] |
PMID: 31158845
|
Clostridium sp. |
Vinpocetine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.49 [FDR-adjusted p-Value=0.027] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Dipyridamole |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.58 [FDR-adjusted p-Value=0.028] |
PMID: 31158845
|
Clostridium sp. |
Dipyridamole |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.512 [FDR-adjusted p-Value=0.032] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Dipyridamole |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.805 [FDR-adjusted p-Value=0.005] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Doxazosin mesylate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.493 [FDR-adjusted p-Value=0.007] |
PMID: 31158845
|
Clostridium sp. |
Doxazosin mesylate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.544 [FDR-adjusted p-Value=0.022] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Doxazosin mesylate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.461 [FDR-adjusted p-Value=0.019] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Enalapril maleate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.439 [FDR-adjusted p-Value=0.009] |
PMID: 31158845
|
Bacteroides xylanisolvens DSM18836 |
Enalapril maleate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.335 [FDR-adjusted p-Value=0.049] |
PMID: 31158845
|
Eubacterium biforme DSM3989 |
Enalapril maleate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.329 [FDR-adjusted p-Value=0.009] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Fluvoxamine maleate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.537 [FDR-adjusted p-Value=0.019] |
PMID: 31158845
|
Clostridium sp. |
Fluvoxamine maleate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.541 [FDR-adjusted p-Value=0.016] |
PMID: 31158845
|
Bifidobacterium ruminatum |
Fluvoxamine maleate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.348 [FDR-adjusted p-Value=0.04] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Sildenafil citrate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.494 [FDR-adjusted p-Value=0.01] |
PMID: 31158845
|
Clostridium sp. |
Sildenafil citrate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.524 [FDR-adjusted p-Value=0.003] |
PMID: 31158845
|
Clostridium difficile 120 |
Sildenafil citrate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.424 [FDR-adjusted p-Value=0.02] |
PMID: 31158845
|
Bacteroides thetaiotaomicron VPI-5482 |
Sumatriptan succinate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.413 [FDR-adjusted p-Value=0.025] |
PMID: 31158845
|
Bacteroides fragilis DS-208 |
Sumatriptan succinate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.623 [FDR-adjusted p-Value=0.006] |
PMID: 31158845
|
Bacteroides fragilis HMW610 |
Sumatriptan succinate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.502 [FDR-adjusted p-Value=0.016] |
PMID: 31158845
|
Bacteroides vulgatus ATCC8482 |
Warfarin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.453 [FDR-adjusted p-Value=0.049] |
PMID: 31158845
|
Bacteroides fragilis HMW615 |
Warfarin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.408 [FDR-adjusted p-Value=0.015] |
PMID: 31158845
|
Bacteroides fragilis ATCC43859 |
Warfarin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.58 [FDR-adjusted p-Value=0.017] |
PMID: 31158845
|
Escherichia coli BW25113 |
Ziprasidone mesylate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.54 [FDR-adjusted p-Value=0.029] |
PMID: 31158845
|
Bacteroides vulgatus ATCC8482 |
Ziprasidone mesylate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.632 [FDR-adjusted p-Value=0.009] |
PMID: 31158845
|
Alistipes indistinctus DSM 22520 |
Ziprasidone mesylate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.689 [FDR-adjusted p-Value=0.022] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Amantadine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.378 [FDR-adjusted p-Value=0.017] |
PMID: 31158845
|
Bifidobacterium ruminatum |
Amantadine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.422 [FDR-adjusted p-Value=0.006] |
PMID: 31158845
|
Bacteroides thetaiotaomicron 7330 |
Amantadine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.347 [FDR-adjusted p-Value=0.013] |
PMID: 31158845
|
Bacteroides fragilis DS-208 |
Amantadine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.325 [FDR-adjusted p-Value=0.013] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Cyclophosphamide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.325 [FDR-adjusted p-Value=0.017] |
PMID: 31158845
|
Alistipes indistinctus DSM 22520 |
Cyclophosphamide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.327 [FDR-adjusted p-Value=0.003] |
PMID: 31158845
|
Eubacterium biforme DSM3989 |
Cyclophosphamide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.34 [FDR-adjusted p-Value=0.032] |
PMID: 31158845
|
Bacteroides fragilis HMW615 |
Cyclophosphamide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.335 [FDR-adjusted p-Value=0.046] |
PMID: 31158845
|
Bacteroides coprophilus DSM18228 |
Ergotamine tartrate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.956 [FDR-adjusted p-Value=0.033] |
PMID: 31158845
|
Bacteroides WH2 WH2 |
Ergotamine tartrate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.774 [FDR-adjusted p-Value=0.017] |
PMID: 31158845
|
Bacteroides thetaiotaomicron 7330 |
Ergotamine tartrate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.23 [FDR-adjusted p-Value=0.024] |
PMID: 31158845
|
Bacteroides fragilis DS-208 |
Ergotamine tartrate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.969 [FDR-adjusted p-Value=0.034] |
PMID: 31158845
|
Escherichia coli BW25113 |
Mefloquine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.977 [FDR-adjusted p-Value=0.034] |
PMID: 31158845
|
Providencia alcalifaciens DSM30120 |
Mefloquine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.464 [FDR-adjusted p-Value=0.035] |
PMID: 31158845
|
Roseburia intestinalis L1-82 |
Mefloquine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.658 [FDR-adjusted p-Value=0.016] |
PMID: 31158845
|
Eggerthella lenta ATCC25559 |
Mefloquine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.995 [FDR-adjusted p-Value=0.012] |
PMID: 31158845
|
Clostridium sp. |
Penbutolol sulfate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.44 [FDR-adjusted p-Value=0.029] |
PMID: 31158845
|
Bacteroides vulgatus ATCC8482 |
Penbutolol sulfate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.48 [FDR-adjusted p-Value=0.021] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Penbutolol sulfate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.442 [FDR-adjusted p-Value=0.02] |
PMID: 31158845
|
Eubacterium biforme DSM3989 |
Penbutolol sulfate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.356 [FDR-adjusted p-Value=0.025] |
PMID: 31158845
|
Clostridium sp. |
Pimozide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.774 [FDR-adjusted p-Value=0.013] |
PMID: 31158845
|
Anaerotruncus colihominis DSM17241 |
Pimozide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.725 [FDR-adjusted p-Value=0.01] |
PMID: 31158845
|
Clostridium bolteae ATCCBAA-613 |
Pimozide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.558 [FDR-adjusted p-Value=0.028] |
PMID: 31158845
|
Akkermansia muciniphila ATCC BAA-835 |
Pimozide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.128 [FDR-adjusted p-Value=0.04] |
PMID: 31158845
|
Bacteroides thetaiotaomicron 3731 |
Tadalafil |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.448 [FDR-adjusted p-Value=0.023] |
PMID: 31158845
|
Bacteroides thetaiotaomicron 7330 |
Tadalafil |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.547 [FDR-adjusted p-Value=0.048] |
PMID: 31158845
|
Bacteroides fragilis HMW610 |
Tadalafil |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.523 [FDR-adjusted p-Value=0.009] |
PMID: 31158845
|
Bacteroides fragilis HMW615 |
Tadalafil |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.434 [FDR-adjusted p-Value=0.041] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Biperiden |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.385 [FDR-adjusted p-Value=0.045] |
PMID: 31158845
|
Clostridium sp. |
Biperiden |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.361 [FDR-adjusted p-Value=0.047] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Biperiden |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.488 [FDR-adjusted p-Value=0.047] |
PMID: 31158845
|
Bacteroides vulgatus ATCC8482 |
Biperiden |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.583 [FDR-adjusted p-Value=0.001] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Methylphenidate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.451 [FDR-adjusted p-Value=0.006] |
PMID: 31158845
|
Clostridium sp. |
Methylphenidate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.538 [FDR-adjusted p-Value=0.006] |
PMID: 31158845
|
Bifidobacterium ruminatum |
Methylphenidate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.373 [FDR-adjusted p-Value=0.042] |
PMID: 31158845
|
Eggerthella lenta ATCC25559 |
Methylphenidate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.433 [FDR-adjusted p-Value=0.012] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Ethopropazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.517 [FDR-adjusted p-Value=0.003] |
PMID: 31158845
|
Clostridium sp. |
Ethopropazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.555 [FDR-adjusted p-Value=0.018] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Ethopropazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.536 [FDR-adjusted p-Value=0.025] |
PMID: 31158845
|
Bacteroides vulgatus ATCC8482 |
Ethopropazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.447 [FDR-adjusted p-Value=0.012] |
PMID: 31158845
|
Odoribacter splanchnius |
Ethopropazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.384 [FDR-adjusted p-Value=0.01] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Phenytoin sodium |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.618 [FDR-adjusted p-Value=0.022] |
PMID: 31158845
|
Bacteroides vulgatus ATCC8482 |
Phenytoin sodium |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.555 [FDR-adjusted p-Value=0.027] |
PMID: 31158845
|
Parabacteroides distasonis ATCC8503 |
Phenytoin sodium |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.364 [FDR-adjusted p-Value=0.02] |
PMID: 31158845
|
Bacteroides xylanisolvens DSM18836 |
Phenytoin sodium |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.326 [FDR-adjusted p-Value=0.002] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Phenytoin sodium |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.48 [FDR-adjusted p-Value=0.021] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Trihexyphenidyl |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.442 [FDR-adjusted p-Value=0.017] |
PMID: 31158845
|
Clostridium sp. |
Trihexyphenidyl |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.526 [FDR-adjusted p-Value=0.031] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Trihexyphenidyl |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.386 [FDR-adjusted p-Value=0.02] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Trihexyphenidyl |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.331 [FDR-adjusted p-Value=0.045] |
PMID: 31158845
|
Bifidobacterium ruminatum |
Trihexyphenidyl |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.402 [FDR-adjusted p-Value=0.013] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Cimetidine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.506 [FDR-adjusted p-Value=0.01] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Cimetidine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.404 [FDR-adjusted p-Value=0.026] |
PMID: 31158845
|
Bacteroides thetaiotaomicron VPI-5482 |
Cimetidine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.512 [FDR-adjusted p-Value=0.017] |
PMID: 31158845
|
Bacteroides thetaiotaomicron 3731 |
Cimetidine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.4 [FDR-adjusted p-Value=0.022] |
PMID: 31158845
|
Bacteroides fragilis 3397 T10 |
Cimetidine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.546 [FDR-adjusted p-Value=0.017] |
PMID: 31158845
|
Bacteroides fragilis T(B)9 |
Cimetidine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.556 [FDR-adjusted p-Value=0.029] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Dasatinib |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.38 [FDR-adjusted p-Value=0.016] |
PMID: 31158845
|
Clostridium sp. |
Dasatinib |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.485 [FDR-adjusted p-Value=0.006] |
PMID: 31158845
|
Clostridium bolteae ATCCBAA-613 |
Dasatinib |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-2.327 [FDR-adjusted p-Value=0.005] |
PMID: 31158845
|
Lactobacillus reuteri CF48-3A BEI HM-102 |
Dasatinib |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.961 [FDR-adjusted p-Value=0.0] |
PMID: 31158845
|
Bifidobacterium ruminatum |
Dasatinib |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.533 [FDR-adjusted p-Value=0.007] |
PMID: 31158845
|
Bacteroides fragilis HMW610 |
Dasatinib |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.482 [FDR-adjusted p-Value=0.004] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Nafronyl oxalate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.409 [FDR-adjusted p-Value=0.049] |
PMID: 31158845
|
Bacteroides vulgatus ATCC8482 |
Nafronyl oxalate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.581 [FDR-adjusted p-Value=0.012] |
PMID: 31158845
|
Bacteroides fragilis NCTC 9343 |
Nafronyl oxalate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.364 [FDR-adjusted p-Value=0.03] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Nafronyl oxalate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.474 [FDR-adjusted p-Value=0.006] |
PMID: 31158845
|
Bifidobacterium ruminatum |
Nafronyl oxalate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.338 [FDR-adjusted p-Value=0.015] |
PMID: 31158845
|
Odoribacter splanchnius |
Nafronyl oxalate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.39 [FDR-adjusted p-Value=0.03] |
PMID: 31158845
|
Odoribacter splanchnius |
Olanzapine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.708 [FDR-adjusted p-Value=0.014] |
PMID: 31158845
|
Bacteroides coprophilus DSM18228 |
Olanzapine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.538 [FDR-adjusted p-Value=0.011] |
PMID: 31158845
|
Bacteroides fragilis 3397 T10 |
Olanzapine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.057 [FDR-adjusted p-Value=0.032] |
PMID: 31158845
|
Bacteroides fragilis T(B)9 |
Olanzapine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.46 [FDR-adjusted p-Value=0.033] |
PMID: 31158845
|
Bacteroides fragilis HMW610 |
Olanzapine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.653 [FDR-adjusted p-Value=0.03] |
PMID: 31158845
|
Bacteroides fragilis HMW615 |
Olanzapine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.653 [FDR-adjusted p-Value=0.041] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Anagrelide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.398 [FDR-adjusted p-Value=0.021] |
PMID: 31158845
|
Clostridium sp. |
Anagrelide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.387 [FDR-adjusted p-Value=0.03] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Anagrelide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.426 [FDR-adjusted p-Value=0.031] |
PMID: 31158845
|
Bacteroides xylanisolvens DSM18836 |
Anagrelide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.329 [FDR-adjusted p-Value=0.028] |
PMID: 31158845
|
Odoribacter splanchnius |
Anagrelide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.431 [FDR-adjusted p-Value=0.032] |
PMID: 31158845
|
Eubacterium biforme DSM3989 |
Anagrelide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.332 [FDR-adjusted p-Value=0.021] |
PMID: 31158845
|
Bacteroides fragilis T(B)9 |
Anagrelide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.346 [FDR-adjusted p-Value=0.041] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Bezafibrate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.382 [FDR-adjusted p-Value=0.031] |
PMID: 31158845
|
Bacteroides vulgatus ATCC8482 |
Bezafibrate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.486 [FDR-adjusted p-Value=0.022] |
PMID: 31158845
|
Bacteroides fragilis NCTC 9343 |
Bezafibrate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.554 [FDR-adjusted p-Value=0.003] |
PMID: 31158845
|
Odoribacter splanchnius |
Bezafibrate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.437 [FDR-adjusted p-Value=0.025] |
PMID: 31158845
|
Parabacteroides merdae ATCC43184 |
Bezafibrate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.362 [FDR-adjusted p-Value=0.011] |
PMID: 31158845
|
Bacteroides fragilis HMW610 |
Bezafibrate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.634 [FDR-adjusted p-Value=0.017] |
PMID: 31158845
|
Bacteroides fragilis ATCC43859 |
Bezafibrate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.709 [FDR-adjusted p-Value=0.017] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Carbetapentane citrate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.451 [FDR-adjusted p-Value=0.008] |
PMID: 31158845
|
Clostridium sp. |
Carbetapentane citrate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.444 [FDR-adjusted p-Value=0.027] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Carbetapentane citrate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.344 [FDR-adjusted p-Value=0.031] |
PMID: 31158845
|
Bacteroides vulgatus ATCC8482 |
Carbetapentane citrate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.335 [FDR-adjusted p-Value=0.041] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Carbetapentane citrate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.43 [FDR-adjusted p-Value=0.023] |
PMID: 31158845
|
Odoribacter splanchnius |
Carbetapentane citrate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.342 [FDR-adjusted p-Value=0.008] |
PMID: 31158845
|
Victivallis vadensis ATCC BAA-548 |
Carbetapentane citrate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.649 [FDR-adjusted p-Value=0.01] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Chlormezanone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.365 [FDR-adjusted p-Value=0.015] |
PMID: 31158845
|
Clostridium sp. |
Chlormezanone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.405 [FDR-adjusted p-Value=0.02] |
PMID: 31158845
|
Bacteroides vulgatus ATCC8482 |
Chlormezanone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.349 [FDR-adjusted p-Value=0.047] |
PMID: 31158845
|
Clostridium asparagiforme DSM15981 |
Chlormezanone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.331 [FDR-adjusted p-Value=0.039] |
PMID: 31158845
|
Bifidobacterium ruminatum |
Chlormezanone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.49 [FDR-adjusted p-Value=0.014] |
PMID: 31158845
|
Alistipes indistinctus DSM 22520 |
Chlormezanone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.349 [FDR-adjusted p-Value=0.026] |
PMID: 31158845
|
Eubacterium biforme DSM3989 |
Chlormezanone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.412 [FDR-adjusted p-Value=0.029] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Dicyclomine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.817 [FDR-adjusted p-Value=0.001] |
PMID: 31158845
|
Bacteroides vulgatus ATCC8482 |
Dicyclomine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.585 [FDR-adjusted p-Value=0.033] |
PMID: 31158845
|
Parabacteroides distasonis ATCC8503 |
Dicyclomine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.394 [FDR-adjusted p-Value=0.012] |
PMID: 31158845
|
Pretovella copri DSM18205 |
Dicyclomine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.373 [FDR-adjusted p-Value=0.013] |
PMID: 31158845
|
Ruminococcus torques ATCC27756 |
Dicyclomine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.695 [FDR-adjusted p-Value=0.016] |
PMID: 31158845
|
Bacteroides xylanisolvens DSM18836 |
Dicyclomine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.461 [FDR-adjusted p-Value=0.007] |
PMID: 31158845
|
Eggerthella lenta ATCC25559 |
Dicyclomine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.546 [FDR-adjusted p-Value=0.007] |
PMID: 31158845
|
Bacteroides eggerthii DSM20697 |
Fenofibrate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.545 [FDR-adjusted p-Value=0.035] |
PMID: 31158845
|
Proteus penneri ATCC35198 |
Fenofibrate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.417 [FDR-adjusted p-Value=0.036] |
PMID: 31158845
|
Pretovella copri DSM18205 |
Fenofibrate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.516 [FDR-adjusted p-Value=0.041] |
PMID: 31158845
|
Clostridium asparagiforme DSM15981 |
Fenofibrate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.559 [FDR-adjusted p-Value=0.034] |
PMID: 31158845
|
Bacteroides fragilis NCTC 9343 |
Fenofibrate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.05 [FDR-adjusted p-Value=0.012] |
PMID: 31158845
|
Clostridium difficile 120 |
Fenofibrate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.308 [FDR-adjusted p-Value=0.016] |
PMID: 31158845
|
Bacteroides fragilis T(B)9 |
Fenofibrate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.855 [FDR-adjusted p-Value=0.038] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Itraconazole |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.527 [FDR-adjusted p-Value=0.034] |
PMID: 31158845
|
Clostridium sp. |
Itraconazole |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.649 [FDR-adjusted p-Value=0.049] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Itraconazole |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.82 [FDR-adjusted p-Value=0.043] |
PMID: 31158845
|
Akkermansia muciniphila ATCC BAA-835 |
Itraconazole |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.067 [FDR-adjusted p-Value=0.022] |
PMID: 31158845
|
Blautia luti DSM14534 |
Itraconazole |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.827 [FDR-adjusted p-Value=0.017] |
PMID: 31158845
|
Odoribacter splanchnius |
Itraconazole |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.136 [FDR-adjusted p-Value=0.034] |
PMID: 31158845
|
Clostridium sporogenes ATCC15579 |
Itraconazole |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.204 [FDR-adjusted p-Value=0.003] |
PMID: 31158845
|
Escherichia coli BW25113 |
Nicergoline |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.477 [FDR-adjusted p-Value=0.011] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Nicergoline |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.433 [FDR-adjusted p-Value=0.034] |
PMID: 31158845
|
Clostridium sp. |
Nicergoline |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.482 [FDR-adjusted p-Value=0.041] |
PMID: 31158845
|
Parabacteroides distasonis ATCC8503 |
Nicergoline |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.69 [FDR-adjusted p-Value=0.018] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Nicergoline |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.698 [FDR-adjusted p-Value=0.036] |
PMID: 31158845
|
Clostridium difficile 120 |
Nicergoline |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-2.744 [FDR-adjusted p-Value=0.007] |
PMID: 31158845
|
Salmonella typhimurium LT2 |
Nicergoline |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.567 [FDR-adjusted p-Value=0.042] |
PMID: 31158845
|
Bacteroides cellulosilyticus DSM14838 |
Ramipril |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.41 [FDR-adjusted p-Value=0.043] |
PMID: 31158845
|
Bacteroides vulgatus ATCC8482 |
Ramipril |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.65 [FDR-adjusted p-Value=0.034] |
PMID: 31158845
|
Bacteroides xylanisolvens DSM18836 |
Ramipril |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.506 [FDR-adjusted p-Value=0.015] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Ramipril |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.76 [FDR-adjusted p-Value=0.029] |
PMID: 31158845
|
Eubacterium biforme DSM3989 |
Ramipril |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.377 [FDR-adjusted p-Value=0.007] |
PMID: 31158845
|
Bacteroides fragilis T(B)9 |
Ramipril |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.441 [FDR-adjusted p-Value=0.045] |
PMID: 31158845
|
Bacteroides fragilis ATCC43859 |
Ramipril |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.692 [FDR-adjusted p-Value=0.017] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Ooscapine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.405 [FDR-adjusted p-Value=0.007] |
PMID: 31158845
|
Ruminococcus torques ATCC27756 |
Ooscapine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.338 [FDR-adjusted p-Value=0.03] |
PMID: 31158845
|
Lactobacillus reuteri CF48-3A BEI HM-102 |
Ooscapine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.343 [FDR-adjusted p-Value=0.035] |
PMID: 31158845
|
Providencia alcalifaciens DSM30120 |
Ooscapine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.322 [FDR-adjusted p-Value=0.003] |
PMID: 31158845
|
Bryantia formatexigens DSM 14469 |
Ooscapine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.457 [FDR-adjusted p-Value=0.007] |
PMID: 31158845
|
Alistipes indistinctus DSM 22520 |
Ooscapine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.378 [FDR-adjusted p-Value=0.011] |
PMID: 31158845
|
Eubacterium biforme DSM3989 |
Ooscapine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.458 [FDR-adjusted p-Value=0.013] |
PMID: 31158845
|
Escherichia coli BW25113 |
Oorgestimate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.713 [FDR-adjusted p-Value=0.031] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Oorgestimate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.162 [FDR-adjusted p-Value=0.008] |
PMID: 31158845
|
Clostridium sp. |
Oorgestimate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.328 [FDR-adjusted p-Value=0.042] |
PMID: 31158845
|
Coprococcus comes ATCC27758 |
Oorgestimate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.324 [FDR-adjusted p-Value=0.016] |
PMID: 31158845
|
Bacteroides fragilis NCTC 9343 |
Oorgestimate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.486 [FDR-adjusted p-Value=0.029] |
PMID: 31158845
|
Bifidobacterium ruminatum |
Oorgestimate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.704 [FDR-adjusted p-Value=0.046] |
PMID: 31158845
|
Eubacterium biforme DSM3989 |
Oorgestimate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.47 [FDR-adjusted p-Value=0.035] |
PMID: 31158845
|
Eggerthella lenta ATCC25559 |
Oorgestimate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.287 [FDR-adjusted p-Value=0.029] |
PMID: 31158845
|
Clostridium hathewayi DSM13479 |
Ranitidine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.443 [FDR-adjusted p-Value=0.006] |
PMID: 31158845
|
Parabacteroides johnsonii DSM18315 |
Ranitidine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.419 [FDR-adjusted p-Value=0.022] |
PMID: 31158845
|
Bifidobacterium breve DSM20213 |
Ranitidine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.878 [FDR-adjusted p-Value=0.005] |
PMID: 31158845
|
Enterococcus faecalis V583 |
Ranitidine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.498 [FDR-adjusted p-Value=0.006] |
PMID: 31158845
|
Bacteroides fragilis T(B)9 |
Ranitidine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.349 [FDR-adjusted p-Value=0.023] |
PMID: 31158845
|
Bacteroides fragilis DS-208 |
Ranitidine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.452 [FDR-adjusted p-Value=0.021] |
PMID: 31158845
|
Bacteroides fragilis HMW610 |
Ranitidine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.442 [FDR-adjusted p-Value=0.014] |
PMID: 31158845
|
Bacteroides fragilis HMW615 |
Ranitidine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.493 [FDR-adjusted p-Value=0.029] |
PMID: 31158845
|
Escherichia coli BW25113 |
Duloxetine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.576 [FDR-adjusted p-Value=0.01] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Duloxetine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.632 [FDR-adjusted p-Value=0.012] |
PMID: 31158845
|
Clostridium sp. |
Duloxetine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.573 [FDR-adjusted p-Value=0.002] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Duloxetine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.455 [FDR-adjusted p-Value=0.014] |
PMID: 31158845
|
Enterobacter cancerogenus ATCC35316 |
Duloxetine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.343 [FDR-adjusted p-Value=0.043] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Duloxetine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.345 [FDR-adjusted p-Value=0.041] |
PMID: 31158845
|
Bacteroides ovatus ATCC8483 |
Duloxetine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.478 [FDR-adjusted p-Value=0.021] |
PMID: 31158845
|
Bacteroides coprophilus DSM18228 |
Duloxetine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.843 [FDR-adjusted p-Value=0.008] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Dexamethasone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.511 [FDR-adjusted p-Value=0.006] |
PMID: 31158845
|
Clostridium scindens ATCC35704 |
Dexamethasone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-6.605 [FDR-adjusted p-Value=0.006] |
PMID: 31158845
|
Bacteroides xylanisolvens DSM18836 |
Dexamethasone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.362 [FDR-adjusted p-Value=0.039] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Dexamethasone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.613 [FDR-adjusted p-Value=0.034] |
PMID: 31158845
|
Bacteroides stercoris ATCC43183 |
Dexamethasone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.336 [FDR-adjusted p-Value=0.029] |
PMID: 31158845
|
Bacteroides thetaiotaomicron VPI-5482 |
Dexamethasone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.363 [FDR-adjusted p-Value=0.031] |
PMID: 31158845
|
Bacteroides fragilis DS-208 |
Dexamethasone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.475 [FDR-adjusted p-Value=0.009] |
PMID: 31158845
|
Bacteroides fragilis HMW610 |
Dexamethasone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.551 [FDR-adjusted p-Value=0.023] |
PMID: 31158845
|
Bacteroides fragilis ATCC43859 |
Dexamethasone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.632 [FDR-adjusted p-Value=0.016] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Glipizide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.778 [FDR-adjusted p-Value=0.022] |
PMID: 31158845
|
Bacteroides fragilis NCTC 9343 |
Glipizide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.751 [FDR-adjusted p-Value=0.035] |
PMID: 31158845
|
Odoribacter splanchnius |
Glipizide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.555 [FDR-adjusted p-Value=0.03] |
PMID: 31158845
|
Bacteroides coprophilus DSM18228 |
Glipizide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.335 [FDR-adjusted p-Value=0.019] |
PMID: 31158845
|
Eubacterium biforme DSM3989 |
Glipizide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.461 [FDR-adjusted p-Value=0.027] |
PMID: 31158845
|
Bacteroides fragilis 3397 T10 |
Glipizide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.62 [FDR-adjusted p-Value=0.019] |
PMID: 31158845
|
Bacteroides fragilis T(B)9 |
Glipizide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.693 [FDR-adjusted p-Value=0.03] |
PMID: 31158845
|
Bacteroides fragilis HMW610 |
Glipizide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.77 [FDR-adjusted p-Value=0.011] |
PMID: 31158845
|
Bacteroides fragilis ATCC43859 |
Glipizide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.801 [FDR-adjusted p-Value=0.016] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Mifepristone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.492 [FDR-adjusted p-Value=0.006] |
PMID: 31158845
|
Clostridium sp. |
Mifepristone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.476 [FDR-adjusted p-Value=0.006] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Mifepristone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.778 [FDR-adjusted p-Value=0.005] |
PMID: 31158845
|
Bacteroides vulgatus ATCC8482 |
Mifepristone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.713 [FDR-adjusted p-Value=0.001] |
PMID: 31158845
|
Bacteroides fragilis NCTC 9343 |
Mifepristone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.504 [FDR-adjusted p-Value=0.045] |
PMID: 31158845
|
Odoribacter splanchnius |
Mifepristone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.348 [FDR-adjusted p-Value=0.012] |
PMID: 31158845
|
Bacteroides fragilis DS-208 |
Mifepristone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.355 [FDR-adjusted p-Value=0.018] |
PMID: 31158845
|
Bacteroides fragilis HMW610 |
Mifepristone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.554 [FDR-adjusted p-Value=0.01] |
PMID: 31158845
|
Bacteroides fragilis ATCC43859 |
Mifepristone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.458 [FDR-adjusted p-Value=0.041] |
PMID: 31158845
|
Bacteroides caccae ATCC43185 |
Pericyazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.937 [FDR-adjusted p-Value=0.025] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Pericyazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.453 [FDR-adjusted p-Value=0.007] |
PMID: 31158845
|
Bacteroides vulgatus ATCC8482 |
Pericyazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.656 [FDR-adjusted p-Value=0.041] |
PMID: 31158845
|
Parabacteroides johnsonii DSM18315 |
Pericyazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.701 [FDR-adjusted p-Value=0.002] |
PMID: 31158845
|
Parabacteroides distasonis ATCC8503 |
Pericyazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.587 [FDR-adjusted p-Value=0.008] |
PMID: 31158845
|
Alistipes indistinctus DSM 22520 |
Pericyazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.857 [FDR-adjusted p-Value=0.05] |
PMID: 31158845
|
Bacteroides thetaiotaomicron 3731 |
Pericyazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.623 [FDR-adjusted p-Value=0.019] |
PMID: 31158845
|
Bacteroides thetaiotaomicron 7330 |
Pericyazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.46 [FDR-adjusted p-Value=0.041] |
PMID: 31158845
|
Bacteroides fragilis HMW610 |
Pericyazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.923 [FDR-adjusted p-Value=0.007] |
PMID: 31158845
|
Escherichia coli BW25113 |
Primaquine phosphate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.364 [FDR-adjusted p-Value=0.018] |
PMID: 31158845
|
Anaerococcus hydrogenalis DSM7454 |
Primaquine phosphate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.531 [FDR-adjusted p-Value=0.005] |
PMID: 31158845
|
Clostridium bolteae ATCCBAA-613 |
Primaquine phosphate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.817 [FDR-adjusted p-Value=0.025] |
PMID: 31158845
|
Clostridium symbiosum ATCC14940 |
Primaquine phosphate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.613 [FDR-adjusted p-Value=0.002] |
PMID: 31158845
|
Clostridium spiroforme DSM1552 |
Primaquine phosphate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.549 [FDR-adjusted p-Value=0.03] |
PMID: 31158845
|
Parabacteroides distasonis ATCC8503 |
Primaquine phosphate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.808 [FDR-adjusted p-Value=0.04] |
PMID: 31158845
|
Bacteroides pectinophilus ATCC43243 |
Primaquine phosphate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.673 [FDR-adjusted p-Value=0.008] |
PMID: 31158845
|
Bifidobacterium breve DSM20213 |
Primaquine phosphate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.605 [FDR-adjusted p-Value=0.043] |
PMID: 31158845
|
Clostridium difficile 120 |
Primaquine phosphate |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.474 [FDR-adjusted p-Value=0.048] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Drospirenone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.706 [FDR-adjusted p-Value=0.002] |
PMID: 31158845
|
Bacteroides vulgatus ATCC8482 |
Drospirenone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.72 [FDR-adjusted p-Value=0.015] |
PMID: 31158845
|
Parabacteroides johnsonii DSM18315 |
Drospirenone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.521 [FDR-adjusted p-Value=0.015] |
PMID: 31158845
|
Bacteroides fragilis NCTC 9343 |
Drospirenone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.561 [FDR-adjusted p-Value=0.007] |
PMID: 31158845
|
Bacteroides xylanisolvens DSM18836 |
Drospirenone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.355 [FDR-adjusted p-Value=0.019] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Drospirenone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.521 [FDR-adjusted p-Value=0.03] |
PMID: 31158845
|
Odoribacter splanchnius |
Drospirenone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.505 [FDR-adjusted p-Value=0.03] |
PMID: 31158845
|
Eubacterium biforme DSM3989 |
Drospirenone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.868 [FDR-adjusted p-Value=0.035] |
PMID: 31158845
|
Bacteroides fragilis HMW610 |
Drospirenone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.68 [FDR-adjusted p-Value=0.012] |
PMID: 31158845
|
Bacteroides fragilis HMW615 |
Drospirenone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.546 [FDR-adjusted p-Value=0.005] |
PMID: 31158845
|
Clostridium sp. |
Eszopiclone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.19 [FDR-adjusted p-Value=0.002] |
PMID: 31158845
|
Collinsella aerofaciens ATCC25986 |
Eszopiclone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.339 [FDR-adjusted p-Value=0.004] |
PMID: 31158845
|
Anaerococcus hydrogenalis DSM7454 |
Eszopiclone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.372 [FDR-adjusted p-Value=0.028] |
PMID: 31158845
|
Clostridium symbiosum ATCC14940 |
Eszopiclone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.324 [FDR-adjusted p-Value=0.034] |
PMID: 31158845
|
Ruminococcus lactaris ATCC29176 |
Eszopiclone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.348 [FDR-adjusted p-Value=0.039] |
PMID: 31158845
|
Eubacterium hallii DSM3353 |
Eszopiclone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.736 [FDR-adjusted p-Value=0.008] |
PMID: 31158845
|
Bacteroides coprophilus DSM18228 |
Eszopiclone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.44 [FDR-adjusted p-Value=0.011] |
PMID: 31158845
|
Eubacterium rectale ATCC33656 |
Eszopiclone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.599 [FDR-adjusted p-Value=0.004] |
PMID: 31158845
|
Bryantia formatexigens DSM 14469 |
Eszopiclone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.429 [FDR-adjusted p-Value=0.009] |
PMID: 31158845
|
Eggerthella lenta ATCC25559 |
Eszopiclone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.458 [FDR-adjusted p-Value=0.011] |
PMID: 31158845
|
Escherichia coli BW25113 |
Fluphenazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.081 [FDR-adjusted p-Value=0.015] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Fluphenazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.555 [FDR-adjusted p-Value=0.015] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Fluphenazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.188 [FDR-adjusted p-Value=0.022] |
PMID: 31158845
|
Bacteroides vulgatus ATCC8482 |
Fluphenazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.906 [FDR-adjusted p-Value=0.008] |
PMID: 31158845
|
Anaerostipes sp. |
Fluphenazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.751 [FDR-adjusted p-Value=0.039] |
PMID: 31158845
|
Eubacterium ventriosum ATCC27560 |
Fluphenazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-3.029 [FDR-adjusted p-Value=0.008] |
PMID: 31158845
|
Parabacteroides distasonis ATCC8503 |
Fluphenazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.37 [FDR-adjusted p-Value=0.016] |
PMID: 31158845
|
Pretovella copri DSM18205 |
Fluphenazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.809 [FDR-adjusted p-Value=0.021] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Fluphenazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.767 [FDR-adjusted p-Value=0.017] |
PMID: 31158845
|
Roseburia intestinalis L1-82 |
Fluphenazine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.81 [FDR-adjusted p-Value=0.042] |
PMID: 31158845
|
Clostridium sp. |
Ketorolac tromethamine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.513 [FDR-adjusted p-Value=0.028] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Ketorolac tromethamine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.76 [FDR-adjusted p-Value=0.008] |
PMID: 31158845
|
Bacteroides vulgatus ATCC8482 |
Ketorolac tromethamine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.636 [FDR-adjusted p-Value=0.008] |
PMID: 31158845
|
Bacteroides fragilis NCTC 9343 |
Ketorolac tromethamine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.651 [FDR-adjusted p-Value=0.002] |
PMID: 31158845
|
Bacteroides xylanisolvens DSM18836 |
Ketorolac tromethamine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.731 [FDR-adjusted p-Value=0.013] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Ketorolac tromethamine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.798 [FDR-adjusted p-Value=0.043] |
PMID: 31158845
|
Bacteroides fragilis T(B)9 |
Ketorolac tromethamine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.71 [FDR-adjusted p-Value=0.024] |
PMID: 31158845
|
Bacteroides fragilis DS-208 |
Ketorolac tromethamine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.737 [FDR-adjusted p-Value=0.029] |
PMID: 31158845
|
Bacteroides fragilis HMW610 |
Ketorolac tromethamine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.74 [FDR-adjusted p-Value=0.042] |
PMID: 31158845
|
Bacteroides fragilis ATCC43859 |
Ketorolac tromethamine |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.764 [FDR-adjusted p-Value=0.034] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Oxybutynin chloride |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.539 [FDR-adjusted p-Value=0.002] |
PMID: 31158845
|
Clostridium sp. |
Oxybutynin chloride |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.614 [FDR-adjusted p-Value=0.003] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Oxybutynin chloride |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.518 [FDR-adjusted p-Value=0.006] |
PMID: 31158845
|
Bacteroides vulgatus ATCC8482 |
Oxybutynin chloride |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.469 [FDR-adjusted p-Value=0.042] |
PMID: 31158845
|
Bacteroides xylanisolvens DSM18836 |
Oxybutynin chloride |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.459 [FDR-adjusted p-Value=0.01] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Oxybutynin chloride |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.545 [FDR-adjusted p-Value=0.01] |
PMID: 31158845
|
Bifidobacterium ruminatum |
Oxybutynin chloride |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.377 [FDR-adjusted p-Value=0.039] |
PMID: 31158845
|
Odoribacter splanchnius |
Oxybutynin chloride |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.362 [FDR-adjusted p-Value=0.019] |
PMID: 31158845
|
Eubacterium biforme DSM3989 |
Oxybutynin chloride |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.336 [FDR-adjusted p-Value=0.016] |
PMID: 31158845
|
Bacteroides fragilis HMW610 |
Oxybutynin chloride |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.593 [FDR-adjusted p-Value=0.023] |
PMID: 31158845
|
Escherichia coli BW25113 |
Paclitaxel |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.507 [FDR-adjusted p-Value=0.01] |
PMID: 31158845
|
Bacteroides xylanisolvens DSM18836 |
Paclitaxel |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.617 [FDR-adjusted p-Value=0.014] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Paclitaxel |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.572 [FDR-adjusted p-Value=0.03] |
PMID: 31158845
|
Odoribacter splanchnius |
Paclitaxel |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.661 [FDR-adjusted p-Value=0.008] |
PMID: 31158845
|
Bacteroides thetaiotaomicron VPI-5482 |
Paclitaxel |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.509 [FDR-adjusted p-Value=0.034] |
PMID: 31158845
|
Bacteroides thetaiotaomicron 3731 |
Paclitaxel |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.411 [FDR-adjusted p-Value=0.049] |
PMID: 31158845
|
Bacteroides thetaiotaomicron 7330 |
Paclitaxel |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.47 [FDR-adjusted p-Value=0.002] |
PMID: 31158845
|
Eggerthella lenta ATCC25559 |
Paclitaxel |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.36 [FDR-adjusted p-Value=0.044] |
PMID: 31158845
|
Bacteroides fragilis DS-208 |
Paclitaxel |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.559 [FDR-adjusted p-Value=0.02] |
PMID: 31158845
|
Bacteroides fragilis HMW615 |
Paclitaxel |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.367 [FDR-adjusted p-Value=0.011] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Repaglinide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.384 [FDR-adjusted p-Value=0.007] |
PMID: 31158845
|
Bacteroides vulgatus ATCC8482 |
Repaglinide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.325 [FDR-adjusted p-Value=0.036] |
PMID: 31158845
|
Bacteroides xylanisolvens DSM18836 |
Repaglinide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.504 [FDR-adjusted p-Value=0.045] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Repaglinide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.748 [FDR-adjusted p-Value=0.024] |
PMID: 31158845
|
Odoribacter splanchnius |
Repaglinide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.38 [FDR-adjusted p-Value=0.023] |
PMID: 31158845
|
Bacteroides thetaiotaomicron 3731 |
Repaglinide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.357 [FDR-adjusted p-Value=0.041] |
PMID: 31158845
|
Bacteroides thetaiotaomicron 7330 |
Repaglinide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.435 [FDR-adjusted p-Value=0.003] |
PMID: 31158845
|
Bacteroides fragilis HMW610 |
Repaglinide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.508 [FDR-adjusted p-Value=0.004] |
PMID: 31158845
|
Bacteroides fragilis HMW615 |
Repaglinide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.508 [FDR-adjusted p-Value=0.004] |
PMID: 31158845
|
Bacteroides fragilis ATCC43859 |
Repaglinide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.517 [FDR-adjusted p-Value=0.04] |
PMID: 31158845
|
Pretovella copri DSM18205 |
Sotalol |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.371 [FDR-adjusted p-Value=0.042] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Sotalol |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.529 [FDR-adjusted p-Value=0.034] |
PMID: 31158845
|
Bacteroides ovatus ATCC8483 |
Sotalol |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.629 [FDR-adjusted p-Value=0.019] |
PMID: 31158845
|
Bacteroides thetaiotaomicron VPI-5482 |
Sotalol |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.545 [FDR-adjusted p-Value=0.044] |
PMID: 31158845
|
Bacteroides thetaiotaomicron 7330 |
Sotalol |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.681 [FDR-adjusted p-Value=0.009] |
PMID: 31158845
|
Bacteroides fragilis 3397 T10 |
Sotalol |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.701 [FDR-adjusted p-Value=0.005] |
PMID: 31158845
|
Bacteroides fragilis DS-208 |
Sotalol |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.629 [FDR-adjusted p-Value=0.021] |
PMID: 31158845
|
Bacteroides fragilis HMW610 |
Sotalol |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.896 [FDR-adjusted p-Value=0.039] |
PMID: 31158845
|
Bacteroides fragilis HMW615 |
Sotalol |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.826 [FDR-adjusted p-Value=0.033] |
PMID: 31158845
|
Bacteroides fragilis ATCC43859 |
Sotalol |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.907 [FDR-adjusted p-Value=0.014] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Zaleplon |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.448 [FDR-adjusted p-Value=0.032] |
PMID: 31158845
|
Clostridium sp. |
Zaleplon |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.438 [FDR-adjusted p-Value=0.01] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Zaleplon |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.807 [FDR-adjusted p-Value=0.013] |
PMID: 31158845
|
Bacteroides vulgatus ATCC8482 |
Zaleplon |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.668 [FDR-adjusted p-Value=0.015] |
PMID: 31158845
|
Bacteroides fragilis NCTC 9343 |
Zaleplon |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.56 [FDR-adjusted p-Value=0.011] |
PMID: 31158845
|
Bacteroides xylanisolvens DSM18836 |
Zaleplon |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.466 [FDR-adjusted p-Value=0.009] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Zaleplon |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.394 [FDR-adjusted p-Value=0.045] |
PMID: 31158845
|
Bacteroides fragilis HMW610 |
Zaleplon |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.519 [FDR-adjusted p-Value=0.014] |
PMID: 31158845
|
Bacteroides fragilis HMW615 |
Zaleplon |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.407 [FDR-adjusted p-Value=0.016] |
PMID: 31158845
|
Bacteroides fragilis ATCC43859 |
Zaleplon |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.568 [FDR-adjusted p-Value=0.041] |
PMID: 31158845
|
Clostridium sp. |
Ezetimibe |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.402 [FDR-adjusted p-Value=0.02] |
PMID: 31158845
|
Bacteroides xylanisolvens DSM18836 |
Ezetimibe |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.511 [FDR-adjusted p-Value=0.03] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Ezetimibe |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.865 [FDR-adjusted p-Value=0.003] |
PMID: 31158845
|
Bacteroides stercoris ATCC43183 |
Ezetimibe |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.541 [FDR-adjusted p-Value=0.021] |
PMID: 31158845
|
Odoribacter splanchnius |
Ezetimibe |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.644 [FDR-adjusted p-Value=0.035] |
PMID: 31158845
|
Clostridium sporogenes ATCC15579 |
Ezetimibe |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.872 [FDR-adjusted p-Value=0.006] |
PMID: 31158845
|
Bacteroides thetaiotaomicron 7330 |
Ezetimibe |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.417 [FDR-adjusted p-Value=0.025] |
PMID: 31158845
|
Bacteroides fragilis 3397 T10 |
Ezetimibe |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.613 [FDR-adjusted p-Value=0.038] |
PMID: 31158845
|
Bacteroides fragilis T(B)9 |
Ezetimibe |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.742 [FDR-adjusted p-Value=0.036] |
PMID: 31158845
|
Bacteroides fragilis DS-208 |
Ezetimibe |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.531 [FDR-adjusted p-Value=0.04] |
PMID: 31158845
|
Bacteroides fragilis HMW615 |
Ezetimibe |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.513 [FDR-adjusted p-Value=0.017] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Gliclazide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.491 [FDR-adjusted p-Value=0.026] |
PMID: 31158845
|
Bacteroides vulgatus ATCC8482 |
Gliclazide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.578 [FDR-adjusted p-Value=0.021] |
PMID: 31158845
|
Parabacteroides distasonis ATCC8503 |
Gliclazide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.375 [FDR-adjusted p-Value=0.005] |
PMID: 31158845
|
Odoribacter splanchnius |
Gliclazide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.411 [FDR-adjusted p-Value=0.019] |
PMID: 31158845
|
Bacteroides thetaiotaomicron 3731 |
Gliclazide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.45 [FDR-adjusted p-Value=0.011] |
PMID: 31158845
|
Bacteroides thetaiotaomicron 7330 |
Gliclazide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.441 [FDR-adjusted p-Value=0.003] |
PMID: 31158845
|
Bacteroides fragilis 3397 T10 |
Gliclazide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.473 [FDR-adjusted p-Value=0.019] |
PMID: 31158845
|
Bacteroides fragilis DS-208 |
Gliclazide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.423 [FDR-adjusted p-Value=0.009] |
PMID: 31158845
|
Bacteroides fragilis HMW610 |
Gliclazide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.498 [FDR-adjusted p-Value=0.045] |
PMID: 31158845
|
Bacteroides fragilis HMW615 |
Gliclazide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.438 [FDR-adjusted p-Value=0.018] |
PMID: 31158845
|
Bacteroides fragilis ATCC43859 |
Gliclazide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.582 [FDR-adjusted p-Value=0.008] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Rebamipide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.852 [FDR-adjusted p-Value=0.004] |
PMID: 31158845
|
Parabacteroides distasonis ATCC8503 |
Rebamipide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.426 [FDR-adjusted p-Value=0.018] |
PMID: 31158845
|
Bacteroides xylanisolvens DSM18836 |
Rebamipide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.737 [FDR-adjusted p-Value=0.004] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Rebamipide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.069 [FDR-adjusted p-Value=0.012] |
PMID: 31158845
|
Bacteroides stercoris ATCC43183 |
Rebamipide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.455 [FDR-adjusted p-Value=0.031] |
PMID: 31158845
|
Bifidobacterium ruminatum |
Rebamipide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.52 [FDR-adjusted p-Value=0.031] |
PMID: 31158845
|
Bacteroides ovatus ATCC8483 |
Rebamipide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.444 [FDR-adjusted p-Value=0.047] |
PMID: 31158845
|
Bacteroides thetaiotaomicron 7330 |
Rebamipide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.72 [FDR-adjusted p-Value=0.011] |
PMID: 31158845
|
Bacteroides fragilis 3397 T10 |
Rebamipide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.529 [FDR-adjusted p-Value=0.019] |
PMID: 31158845
|
Bacteroides fragilis HMW610 |
Rebamipide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.759 [FDR-adjusted p-Value=0.037] |
PMID: 31158845
|
Bacteroides fragilis HMW615 |
Rebamipide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.767 [FDR-adjusted p-Value=0.01] |
PMID: 31158845
|
Escherichia coli BW25113 |
Sulfinpyrazone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.511 [FDR-adjusted p-Value=0.035] |
PMID: 31158845
|
Parabacteroides johnsonii DSM18315 |
Sulfinpyrazone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.402 [FDR-adjusted p-Value=0.039] |
PMID: 31158845
|
Bacteroides fragilis NCTC 9343 |
Sulfinpyrazone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.582 [FDR-adjusted p-Value=0.029] |
PMID: 31158845
|
Bacteroides xylanisolvens DSM18836 |
Sulfinpyrazone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.544 [FDR-adjusted p-Value=0.034] |
PMID: 31158845
|
Odoribacter splanchnius |
Sulfinpyrazone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.638 [FDR-adjusted p-Value=0.012] |
PMID: 31158845
|
Bacteroides thetaiotaomicron 7330 |
Sulfinpyrazone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.443 [FDR-adjusted p-Value=0.048] |
PMID: 31158845
|
Eggerthella lenta ATCC25559 |
Sulfinpyrazone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.912 [FDR-adjusted p-Value=0.043] |
PMID: 31158845
|
Bacteroides fragilis DS-208 |
Sulfinpyrazone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.546 [FDR-adjusted p-Value=0.017] |
PMID: 31158845
|
Bacteroides fragilis HMW610 |
Sulfinpyrazone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.681 [FDR-adjusted p-Value=0.025] |
PMID: 31158845
|
Bacteroides fragilis HMW615 |
Sulfinpyrazone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.56 [FDR-adjusted p-Value=0.017] |
PMID: 31158845
|
Bacteroides fragilis ATCC43859 |
Sulfinpyrazone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.724 [FDR-adjusted p-Value=0.044] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Etodolac |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.406 [FDR-adjusted p-Value=0.044] |
PMID: 31158845
|
Bacteroides xylanisolvens DSM18836 |
Etodolac |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.579 [FDR-adjusted p-Value=0.034] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Etodolac |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.791 [FDR-adjusted p-Value=0.012] |
PMID: 31158845
|
Odoribacter splanchnius |
Etodolac |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.51 [FDR-adjusted p-Value=0.007] |
PMID: 31158845
|
Bacteroides thetaiotaomicron VPI-5482 |
Etodolac |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.473 [FDR-adjusted p-Value=0.008] |
PMID: 31158845
|
Bacteroides thetaiotaomicron 3731 |
Etodolac |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.4 [FDR-adjusted p-Value=0.009] |
PMID: 31158845
|
Bacteroides thetaiotaomicron 7330 |
Etodolac |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.474 [FDR-adjusted p-Value=0.031] |
PMID: 31158845
|
Bacteroides fragilis 3397 T10 |
Etodolac |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.374 [FDR-adjusted p-Value=0.041] |
PMID: 31158845
|
Bacteroides fragilis T(B)9 |
Etodolac |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.596 [FDR-adjusted p-Value=0.016] |
PMID: 31158845
|
Bacteroides fragilis DS-208 |
Etodolac |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.614 [FDR-adjusted p-Value=0.023] |
PMID: 31158845
|
Bacteroides fragilis HMW615 |
Etodolac |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.783 [FDR-adjusted p-Value=0.042] |
PMID: 31158845
|
Bacteroides fragilis ATCC43859 |
Etodolac |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.814 [FDR-adjusted p-Value=0.015] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Finasteride |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.723 [FDR-adjusted p-Value=0.002] |
PMID: 31158845
|
Bacteroides vulgatus ATCC8482 |
Finasteride |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.735 [FDR-adjusted p-Value=0.007] |
PMID: 31158845
|
Parabacteroides distasonis ATCC8503 |
Finasteride |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.392 [FDR-adjusted p-Value=0.004] |
PMID: 31158845
|
Bacteroides fragilis NCTC 9343 |
Finasteride |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.592 [FDR-adjusted p-Value=0.031] |
PMID: 31158845
|
Bacteroides xylanisolvens DSM18836 |
Finasteride |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.587 [FDR-adjusted p-Value=0.004] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Finasteride |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.589 [FDR-adjusted p-Value=0.007] |
PMID: 31158845
|
Akkermansia muciniphila ATCC BAA-835 |
Finasteride |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-4.039 [FDR-adjusted p-Value=0.002] |
PMID: 31158845
|
Odoribacter splanchnius |
Finasteride |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.496 [FDR-adjusted p-Value=0.025] |
PMID: 31158845
|
Bacteroides fragilis DS-208 |
Finasteride |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.54 [FDR-adjusted p-Value=0.034] |
PMID: 31158845
|
Bacteroides fragilis HMW610 |
Finasteride |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.668 [FDR-adjusted p-Value=0.002] |
PMID: 31158845
|
Bacteroides fragilis HMW615 |
Finasteride |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.564 [FDR-adjusted p-Value=0.024] |
PMID: 31158845
|
Bacteroides fragilis ATCC43859 |
Finasteride |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.706 [FDR-adjusted p-Value=0.009] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Galantamine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.495 [FDR-adjusted p-Value=0.002] |
PMID: 31158845
|
Bacteroides ovatus ATCC8483 |
Galantamine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.494 [FDR-adjusted p-Value=0.011] |
PMID: 31158845
|
Bacteroides coprophilus DSM18228 |
Galantamine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.578 [FDR-adjusted p-Value=0.03] |
PMID: 31158845
|
Bacteroides thetaiotaomicron VPI-5482 |
Galantamine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.627 [FDR-adjusted p-Value=0.004] |
PMID: 31158845
|
Bacteroides thetaiotaomicron 3731 |
Galantamine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.453 [FDR-adjusted p-Value=0.019] |
PMID: 31158845
|
Bacteroides thetaiotaomicron 7330 |
Galantamine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.589 [FDR-adjusted p-Value=0.018] |
PMID: 31158845
|
Bacteroides fragilis 3397 T10 |
Galantamine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.519 [FDR-adjusted p-Value=0.006] |
PMID: 31158845
|
Bacteroides fragilis T(B)9 |
Galantamine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.457 [FDR-adjusted p-Value=0.01] |
PMID: 31158845
|
Bacteroides fragilis DS-208 |
Galantamine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.563 [FDR-adjusted p-Value=0.007] |
PMID: 31158845
|
Bacteroides fragilis HMW610 |
Galantamine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.67 [FDR-adjusted p-Value=0.007] |
PMID: 31158845
|
Bacteroides fragilis HMW615 |
Galantamine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.594 [FDR-adjusted p-Value=0.011] |
PMID: 31158845
|
Bacteroides fragilis ATCC43859 |
Galantamine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.71 [FDR-adjusted p-Value=0.002] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Griseofulvin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.69 [FDR-adjusted p-Value=0.039] |
PMID: 31158845
|
Bacteroides vulgatus ATCC8482 |
Griseofulvin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.782 [FDR-adjusted p-Value=0.025] |
PMID: 31158845
|
Parabacteroides distasonis ATCC8503 |
Griseofulvin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.503 [FDR-adjusted p-Value=0.024] |
PMID: 31158845
|
Bacteroides fragilis NCTC 9343 |
Griseofulvin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.721 [FDR-adjusted p-Value=0.018] |
PMID: 31158845
|
Bacteroides xylanisolvens DSM18836 |
Griseofulvin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.54 [FDR-adjusted p-Value=0.007] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Griseofulvin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.76 [FDR-adjusted p-Value=0.016] |
PMID: 31158845
|
Bacteroides thetaiotaomicron VPI-5482 |
Griseofulvin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.419 [FDR-adjusted p-Value=0.03] |
PMID: 31158845
|
Bacteroides fragilis 3397 T10 |
Griseofulvin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.588 [FDR-adjusted p-Value=0.029] |
PMID: 31158845
|
Bacteroides fragilis T(B)9 |
Griseofulvin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.609 [FDR-adjusted p-Value=0.038] |
PMID: 31158845
|
Bacteroides fragilis DS-208 |
Griseofulvin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.666 [FDR-adjusted p-Value=0.037] |
PMID: 31158845
|
Bacteroides fragilis HMW615 |
Griseofulvin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.585 [FDR-adjusted p-Value=0.028] |
PMID: 31158845
|
Bacteroides fragilis ATCC43859 |
Griseofulvin |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.778 [FDR-adjusted p-Value=0.017] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Metaxalone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.579 [FDR-adjusted p-Value=0.048] |
PMID: 31158845
|
Clostridium sp. |
Metaxalone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.53 [FDR-adjusted p-Value=0.032] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Metaxalone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.828 [FDR-adjusted p-Value=0.007] |
PMID: 31158845
|
Bacteroides vulgatus ATCC8482 |
Metaxalone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.764 [FDR-adjusted p-Value=0.008] |
PMID: 31158845
|
Parabacteroides distasonis ATCC8503 |
Metaxalone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.483 [FDR-adjusted p-Value=0.021] |
PMID: 31158845
|
Bacteroides pectinophilus ATCC43243 |
Metaxalone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.525 [FDR-adjusted p-Value=0.034] |
PMID: 31158845
|
Bacteroides fragilis NCTC 9343 |
Metaxalone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.632 [FDR-adjusted p-Value=0.047] |
PMID: 31158845
|
Bacteroides xylanisolvens DSM18836 |
Metaxalone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.633 [FDR-adjusted p-Value=0.039] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Metaxalone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.694 [FDR-adjusted p-Value=0.017] |
PMID: 31158845
|
Bacteroides fragilis HMW610 |
Metaxalone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.654 [FDR-adjusted p-Value=0.005] |
PMID: 31158845
|
Bacteroides fragilis HMW615 |
Metaxalone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.654 [FDR-adjusted p-Value=0.044] |
PMID: 31158845
|
Bacteroides fragilis ATCC43859 |
Metaxalone |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.76 [FDR-adjusted p-Value=0.014] |
PMID: 31158845
|
Pretovella copri DSM18205 |
Naloxone |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.366 [FDR-adjusted p-Value=0.04] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Naloxone |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.694 [FDR-adjusted p-Value=0.005] |
PMID: 31158845
|
Bacteroides ovatus ATCC8483 |
Naloxone |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.722 [FDR-adjusted p-Value=0.009] |
PMID: 31158845
|
Bacteroides coprophilus DSM18228 |
Naloxone |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.98 [FDR-adjusted p-Value=0.02] |
PMID: 31158845
|
Bacteroides thetaiotaomicron VPI-5482 |
Naloxone |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.663 [FDR-adjusted p-Value=0.009] |
PMID: 31158845
|
Bacteroides thetaiotaomicron 3731 |
Naloxone |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.548 [FDR-adjusted p-Value=0.045] |
PMID: 31158845
|
Bacteroides thetaiotaomicron 7330 |
Naloxone |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.723 [FDR-adjusted p-Value=0.009] |
PMID: 31158845
|
Bacteroides fragilis 3397 T10 |
Naloxone |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.924 [FDR-adjusted p-Value=0.011] |
PMID: 31158845
|
Bacteroides fragilis T(B)9 |
Naloxone |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.839 [FDR-adjusted p-Value=0.018] |
PMID: 31158845
|
Bacteroides fragilis DS-208 |
Naloxone |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.898 [FDR-adjusted p-Value=0.011] |
PMID: 31158845
|
Bacteroides fragilis HMW610 |
Naloxone |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-3.708 [FDR-adjusted p-Value=0.0] |
PMID: 31158845
|
Bacteroides fragilis ATCC43859 |
Naloxone |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-5.155 [FDR-adjusted p-Value=0.016] |
PMID: 31158845
|
Bacteroides vulgatus ATCC8482 |
Naproxen(+) |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.455 [FDR-adjusted p-Value=0.02] |
PMID: 31158845
|
Parabacteroides distasonis ATCC8503 |
Naproxen(+) |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.337 [FDR-adjusted p-Value=0.007] |
PMID: 31158845
|
Bacteroides xylanisolvens DSM18836 |
Naproxen(+) |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.376 [FDR-adjusted p-Value=0.039] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Naproxen(+) |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.454 [FDR-adjusted p-Value=0.005] |
PMID: 31158845
|
Odoribacter splanchnius |
Naproxen(+) |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.453 [FDR-adjusted p-Value=0.004] |
PMID: 31158845
|
Bacteroides thetaiotaomicron 3731 |
Naproxen(+) |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.364 [FDR-adjusted p-Value=0.012] |
PMID: 31158845
|
Bacteroides thetaiotaomicron 7330 |
Naproxen(+) |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.362 [FDR-adjusted p-Value=0.006] |
PMID: 31158845
|
Bacteroides fragilis 3397 T10 |
Naproxen(+) |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.447 [FDR-adjusted p-Value=0.032] |
PMID: 31158845
|
Bacteroides fragilis T(B)9 |
Naproxen(+) |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.387 [FDR-adjusted p-Value=0.005] |
PMID: 31158845
|
Bacteroides fragilis HMW610 |
Naproxen(+) |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.654 [FDR-adjusted p-Value=0.024] |
PMID: 31158845
|
Bacteroides fragilis HMW615 |
Naproxen(+) |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.569 [FDR-adjusted p-Value=0.039] |
PMID: 31158845
|
Bacteroides fragilis ATCC43859 |
Naproxen(+) |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.765 [FDR-adjusted p-Value=0.011] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Neostigmine bromide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.528 [FDR-adjusted p-Value=0.003] |
PMID: 31158845
|
Bacteroides fragilis NCTC 9343 |
Neostigmine bromide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.611 [FDR-adjusted p-Value=0.007] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Neostigmine bromide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.568 [FDR-adjusted p-Value=0.001] |
PMID: 31158845
|
Bacteroides ovatus ATCC8483 |
Neostigmine bromide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.62 [FDR-adjusted p-Value=0.003] |
PMID: 31158845
|
Parabacteroides merdae ATCC43184 |
Neostigmine bromide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.342 [FDR-adjusted p-Value=0.003] |
PMID: 31158845
|
Bacteroides coprophilus DSM18228 |
Neostigmine bromide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.533 [FDR-adjusted p-Value=0.006] |
PMID: 31158845
|
Bacteroides thetaiotaomicron VPI-5482 |
Neostigmine bromide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.515 [FDR-adjusted p-Value=0.008] |
PMID: 31158845
|
Bacteroides thetaiotaomicron 3731 |
Neostigmine bromide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.352 [FDR-adjusted p-Value=0.009] |
PMID: 31158845
|
Bacteroides thetaiotaomicron 7330 |
Neostigmine bromide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.598 [FDR-adjusted p-Value=0.035] |
PMID: 31158845
|
Bacteroides fragilis 3397 T10 |
Neostigmine bromide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.693 [FDR-adjusted p-Value=0.003] |
PMID: 31158845
|
Bacteroides fragilis T(B)9 |
Neostigmine bromide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.535 [FDR-adjusted p-Value=0.011] |
PMID: 31158845
|
Bacteroides fragilis DS-208 |
Neostigmine bromide |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.584 [FDR-adjusted p-Value=0.013] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Telmisartan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.999 [FDR-adjusted p-Value=0.006] |
PMID: 31158845
|
Bacteroides cellulosilyticus DSM14838 |
Telmisartan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.567 [FDR-adjusted p-Value=0.035] |
PMID: 31158845
|
Bacteroides vulgatus ATCC8482 |
Telmisartan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.856 [FDR-adjusted p-Value=0.026] |
PMID: 31158845
|
Parabacteroides distasonis ATCC8503 |
Telmisartan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.73 [FDR-adjusted p-Value=0.034] |
PMID: 31158845
|
Bacteroides fragilis NCTC 9343 |
Telmisartan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.886 [FDR-adjusted p-Value=0.041] |
PMID: 31158845
|
Bacteroides xylanisolvens DSM18836 |
Telmisartan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.784 [FDR-adjusted p-Value=0.03] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Telmisartan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.005 [FDR-adjusted p-Value=0.009] |
PMID: 31158845
|
Bacteroides stercoris ATCC43183 |
Telmisartan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.599 [FDR-adjusted p-Value=0.04] |
PMID: 31158845
|
Odoribacter splanchnius |
Telmisartan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.402 [FDR-adjusted p-Value=0.035] |
PMID: 31158845
|
Bacteroides ovatus ATCC8483 |
Telmisartan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.349 [FDR-adjusted p-Value=0.029] |
PMID: 31158845
|
Bacteroides thetaiotaomicron 7330 |
Telmisartan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.619 [FDR-adjusted p-Value=0.022] |
PMID: 31158845
|
Bacteroides fragilis HMW610 |
Telmisartan |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.615 [FDR-adjusted p-Value=0.017] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Colchicine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.371 [FDR-adjusted p-Value=0.002] |
PMID: 31158845
|
Clostridium sp. |
Colchicine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.408 [FDR-adjusted p-Value=0.033] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Colchicine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.647 [FDR-adjusted p-Value=0.004] |
PMID: 31158845
|
Bacteroides vulgatus ATCC8482 |
Colchicine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.559 [FDR-adjusted p-Value=0.028] |
PMID: 31158845
|
Parabacteroides johnsonii DSM18315 |
Colchicine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.365 [FDR-adjusted p-Value=0.048] |
PMID: 31158845
|
Bacteroides fragilis NCTC 9343 |
Colchicine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.53 [FDR-adjusted p-Value=0.034] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Colchicine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.56 [FDR-adjusted p-Value=0.004] |
PMID: 31158845
|
Odoribacter splanchnius |
Colchicine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.359 [FDR-adjusted p-Value=0.021] |
PMID: 31158845
|
Bacteroides fragilis 3397 T10 |
Colchicine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.533 [FDR-adjusted p-Value=0.024] |
PMID: 31158845
|
Bacteroides fragilis T(B)9 |
Colchicine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.495 [FDR-adjusted p-Value=0.033] |
PMID: 31158845
|
Bacteroides fragilis DS-208 |
Colchicine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.459 [FDR-adjusted p-Value=0.004] |
PMID: 31158845
|
Bacteroides fragilis HMW610 |
Colchicine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.502 [FDR-adjusted p-Value=0.01] |
PMID: 31158845
|
Bacteroides fragilis ATCC43859 |
Colchicine |
Therapeutic Substance; Herbal Substance |
Approved Drug; Medicinal Herbal Compounds |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.574 [FDR-adjusted p-Value=0.026] |
PMID: 31158845
|
Blautia hansenii DSM20583 |
Diltiazem |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.448 [FDR-adjusted p-Value=0.043] |
PMID: 31158845
|
Clostridium sp. |
Diltiazem |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.396 [FDR-adjusted p-Value=0.044] |
PMID: 31158845
|
Bacteroides dorei DSM17855 |
Diltiazem |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.478 [FDR-adjusted p-Value=0.011] |
PMID: 31158845
|
Parabacteroides johnsonii DSM18315 |
Diltiazem |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.599 [FDR-adjusted p-Value=0.012] |
PMID: 31158845
|
Parabacteroides distasonis ATCC8503 |
Diltiazem |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.828 [FDR-adjusted p-Value=0.003] |
PMID: 31158845
|
Bacteroides xylanisolvens DSM18836 |
Diltiazem |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-2.781 [FDR-adjusted p-Value=0.001] |
PMID: 31158845
|
Bacteroides uniformis ATCC8492 |
Diltiazem |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.469 [FDR-adjusted p-Value=0.02] |
PMID: 31158845
|
Bacteroides ovatus ATCC8483 |
Diltiazem |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-1.207 [FDR-adjusted p-Value=0.004] |
PMID: 31158845
|
Alistipes indistinctus DSM 22520 |
Diltiazem |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High-throughput incubation assays |
n.a. |
n.a. |
Metabolism significantly decreased the drug concentration by: log2(fold change)=-0.401 [FDR-adjusted p-Value=0.025] |
PMID: 31158845
|
Bacteroides thetaiotaomicron VPI-5482 |
Diltiazem |
Therapeutic Substance |
Approved Drug |
n.a. |
n.a. |
n.a. |
High |