Ipriflavone as an inhibitor of human cytochrome P450 enzymes-Reference-Cited by-同舟云学术

Ipriflavone as an inhibitor of human cytochrome P450 enzymes

Published:1998-02 Issue:4 Volume:123 Page:605-610
ISSN:0007-1188
Container-title:British Journal of Pharmacology
language:en
Short-container-title:

Author:

Monostory Katalin,Vereczkey László,Lévai Ferenc,Szatmári István

Publisher

Wiley

Subject

Pharmacology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1038/sj.bjp.0701633/fullpdf

Reference21 articles.

1. Flavonoids as inhibitors of rat liver monooxygenase activities;Beyeler;Biochem. Pharmacol.,1988

2. Expression of a human liver cytochrome P-450 protein with tolbutamide hydroxylase activity in Saccharomyces cerevsiae;Brian;Biochemistry,1989

3. Metabolic oxidation of the carcinogens 4-aminobiphenyl and 4,4′-methylene-bis(2-chloroaniline) by human hepatic microsomes and by purified rat hepatic cytochrome P-450 monooxygenases;Butler;Cancer Res.,1989a

4. Human cytochrome P-450Pa (P-450Ia2), the phenacetin O-deethylase, is primarily responsible for the hepatic 3-demethylation of caffeine and N-oxidation of carcinogenic arylamines;Butler;Proc. Natl. Acad. Sci. U.S.A.,1989b

5. Characterization of rat and human liver microsomal cytochrome P-450 forms involved in nifedipine oxidation, a prototype for genetic polymorphism in oxidative drug metabolism;Guengerich;J. Biol. Chem.,1986

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