Human-liver cytochromes P-450 involved in polymorphisms of drug oxidation-Reference-Cited by-同舟云学术

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Human-liver cytochromes P-450 involved in polymorphisms of drug oxidation

Published:1986-01 Issue:5 Volume:16 Page:367-378
ISSN:0049-8254
Container-title:Xenobiotica
language:en
Short-container-title:Xenobiotica

Author:

Guengerich F. P.,Distlerath L. M.,Reilly P. E. B.,Wolff T.,Shimada T.,Umbenhauer D. R.,Martin M. V.

Publisher

Informa UK Limited

Subject

Health, Toxicology and Mutagenesis,Pharmacology,Toxicology,Biochemistry,General Medicine

Link

http://www.tandfonline.com/doi/pdf/10.3109/00498258609050245

Reference18 articles.

1. Animal modelling of human polymorphic drug oxidation—the metabolism of debrisoquine and phenacetin in rat inbred strains

2. Evidence for an enzymatic defect in the 4-hydroxylation of debrisoquine by human liver.

3. Characterization of a human liver cytochrome P-450 involved in the oxidation of debrisoquine and other drugs by using antibodies raised to the analogous rat enzyme.

4. Isolation and purification of cytochrome P-450, and the existence of multiple forms

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1. Next Generation Sequencing in Oncological Diagnostics: Hype or Hope?;Journal of Biosciences and Medicines;2024

2. CYP3As catalyze nifedipine oxidation in pig liver microsomes: Enzyme kinetics, inhibition and functional expression;Catalysis Communications;2011-03

3. Interactions of mammalian cytochrome P450, NADPH-cytochrome P450 reductase, and cytochrome b5 enzymes;Archives of Biochemistry and Biophysics;2005-03

4. Roles of Human Cytochrome P450 Enzymes Involved in Drug Metabolism and Toxicological Studies;YAKUGAKU ZASSHI;2000

5. Effects of cytochrome P450 inducers on 17α-ethinyloestradiol (EE2 ) conjugation by primary human hepatocytes;British Journal of Clinical Pharmacology;1999-11

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