Results 201 to 210 of about 852,116 (265)
Improved Prediction of CYP2D6 Catalyzed Drug Metabolism by Taking Variant Substrate Specificities and Novel Polymorphic Haplotypes into Account. [PDF]
Johansson I +11 more
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Examining the Impact of Diet-and-Exercise-Induced Weight Loss on Drug Metabolism and Gastric Emptying in Patients with Obesity. [PDF]
Liu S +8 more
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Advanced Liver-on-a-Chip Model for Evaluating Drug Metabolism and Hepatotoxicity. [PDF]
Frojdenfal S, Zuchowska A.
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CYP3A4 and CYP3A5: the crucial roles in clinical drug metabolism and the significant implications of genetic polymorphisms. [PDF]
Zhang Y +7 more
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Metabolism, Pharmacogenetics, and Metabolic Drug–Drug Interactions of Antipsychotic Drugs
Cellular and Molecular Neurobiology, 19991. Antipsychotic drugs are extensively metabolised by cytochrome P450 (CYP) enzymes. 2. Dispositions of a number of antipsychotic drugs have been shown to cosegregate with polymorphism of CYP2D6. 3. Metabolic drug-drug interactions have frequently been observed when antipsychotics are coadministered with other drugs. 4.
J, Fang, J W, Gorrod
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REVERSIBLE METABOLISM OF DRUGS
Drug Metabolism and Drug Interactions, 1994Many drugs undergo reversible metabolism. The basis of our understanding of this process is the reversible metabolism of prednisone (PD)-prednisolone (PL). The pharmacokinetics of reversible metabolism requires the use of four area under the curve values integrated into four equations for clearance (CL).
M W, Jann +3 more
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Drug metabolism and pharmacokinetics
Drug Metabolism Reviews, 2009In this article, aspects of absorption, distribution, metabolism, and excretion have been described bearing in mind the pathogenesis of allergic diseases and their possible therapeutic opportunities. The importance of the routes of administration of the different therapeutic groups has been emphasized.
Margherita Strolin, Benedetti +7 more
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Clinical Pharmacology & Therapeutics, 1973
Measurable catalysis of mixed‐function oxidations of foreign organic compounds in human placental tissues appears to occur only with a limited number of substrates including 3,4‐benzpyrene, 3'‐methyl‐4‐monomethylaminoazobenzene, and N‐monomethylaniline. Evidence now indicates that mixed‐function oxidations of the classical “type 1” drug substrates (the
M R, Juchau +3 more
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Measurable catalysis of mixed‐function oxidations of foreign organic compounds in human placental tissues appears to occur only with a limited number of substrates including 3,4‐benzpyrene, 3'‐methyl‐4‐monomethylaminoazobenzene, and N‐monomethylaniline. Evidence now indicates that mixed‐function oxidations of the classical “type 1” drug substrates (the
M R, Juchau +3 more
openaire +2 more sources

