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Volumn 1, Issue 4, 2001, Pages 288-292
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CYP2C9*3 influences the metabolism and the drug-interaction of candesartan in vitro
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Author keywords
Candesartan; CYP2C9; In vitro; Inhibition; Metabolism; Polymorphism; Warfarin
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Indexed keywords
ANTICOAGULANT AGENT;
ANTIHYPERTENSIVE AGENT;
BENZIMIDAZOLE DERIVATIVE;
CANDESARTAN;
CYP2C9 PROTEIN, HUMAN;
CYTOCHROME P450;
LEUCINE;
RECOMBINANT PROTEIN;
STEROID 16ALPHA MONOOXYGENASE;
STEROID MONOOXYGENASE;
TETRAZOLE DERIVATIVE;
UNSPECIFIC MONOOXYGENASE;
WARFARIN;
ALLELE;
ARTICLE;
DOSE RESPONSE;
DRUG INTERACTION;
ENZYMOLOGY;
GENETICS;
HUMAN;
LIVER MICROSOME;
METABOLISM;
PHYSIOLOGY;
SACCHAROMYCES CEREVISIAE;
ALLELES;
ANTICOAGULANTS;
ANTIHYPERTENSIVE AGENTS;
ARYL HYDROCARBON HYDROXYLASES;
BENZIMIDAZOLES;
CYTOCHROME P-450 ENZYME SYSTEM;
DOSE-RESPONSE RELATIONSHIP, DRUG;
DRUG INTERACTIONS;
HUMANS;
LEUCINE;
MICROSOMES, LIVER;
RECOMBINANT PROTEINS;
SACCHAROMYCES CEREVISIAE;
STEROID 16-ALPHA-HYDROXYLASE;
STEROID HYDROXYLASES;
TETRAZOLES;
WARFARIN;
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EID: 0035753492
PISSN: 1470269X
EISSN: None
Source Type: Journal
DOI: 10.1038/sj.tpj.6500063 Document Type: Article |
Times cited : (27)
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References (5)
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