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Volumn 64, Issue 3-4, 2010, Pages 120-122
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The role of polymorphic cytochrome P450 enzymes in drug design, development and drug interactions with a special emphasis on phenotyping
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Author keywords
Cytochrome P450; Drug design; Metabolism; Pharmacogenetis; Phenotyping
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Indexed keywords
CYTOCHROME P450;
DRUG DESIGN;
DRUG METABOLISMS;
GENETIC POLYMORPHISMS;
PHENOTYPING;
POLYMORPHIC CYTOCHROME;
THERAPEUTIC FAILURE;
DESIGN;
METABOLISM;
DRUG INTERACTIONS;
ANASTROZOLE;
CYTOCHROME P450;
CYTOCHROME P450 1A1;
CYTOCHROME P450 1A2;
CYTOCHROME P450 2A6;
CYTOCHROME P450 2B6;
CYTOCHROME P450 2C8;
CYTOCHROME P450 2D6;
CYTOCHROME P450 2E1;
CYTOCHROME P450 3A4;
DRUG METABOLITE;
DRUG METABOLIZING ENZYME;
ENDOXIFEN;
FADROZOLE;
KETOCONAZOLE;
LANOSTEROL;
LETROZOLE;
PAROXETINE;
POLYCHLORINATED BIPHENYL DERIVATIVE;
POLYCYCLIC AROMATIC HYDROCARBON;
TAMOXIFEN;
UNCLASSIFIED DRUG;
BREAST CANCER;
BREAST TUMOR;
CARCINOGENICITY;
CHEMICAL CARCINOGENESIS;
COMPETITIVE INHIBITION;
DRUG ANTAGONISM;
DRUG BLOOD LEVEL;
DRUG DESIGN;
DRUG EFFICACY;
DRUG METABOLISM;
DRUG TARGETING;
ENZYME POLYMORPHISM;
ETHNIC DIFFERENCE;
GENE DELETION;
GENE MUTATION;
HUMAN;
MYCOSIS;
PHARMACOGENETICS;
PHENOTYPE;
PRODUCT DEVELOPMENT;
PROSTATE CANCER;
REVIEW;
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EID: 77951977439
PISSN: 13811177
EISSN: None
Source Type: Journal
DOI: 10.1016/j.molcatb.2009.03.020 Document Type: Review |
Times cited : (13)
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References (23)
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