Kinetic studies of inhibition of estradiol 2-and 16α-hydroxylases in rat liver microsomes with various cytochrome P-450 inhibitors
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Biochemistry
Reference32 articles.
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3. Nuclear binding and retention of the receptor estrogen complex: Relation to the agonistic and antagonistic properties of estradiol;Clark;Endocrinology,1977
4. Biological properties of 16α-hydroxyestrone: Implications in estrogen physiology and pathophysiology;Fishman;J. clin. Endocr. Metab.,1980
5. Catecholestrogens-Chemistry, biogenesis, metabolism, occurrence and physiological significance;Ball;Acta endocr., Copnh,1980
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1. Equine cytochrome P450 aromatase exhibits an estrogen 2-hydroxylase activity in vitro;The Journal of Steroid Biochemistry and Molecular Biology;1996-09
2. P450 enzymes of estrogen metabolism;Pharmacology & Therapeutics;1993-01
3. The Role of Mixed Function Oxidase (Mfo) in the Metabolism of the Spin Trapping Agent α-Phenyl-N-Tert-Butyl-Nitrone (Pbn) in RATS;Free Radical Research Communications;1991-01
4. Antidepressant-like effects of trazodone on a behavioral screen are mediated by trazodone, not the metabolite m-chlorophenylpiperazine;European Journal of Pharmacology;1990-02
5. 2-bromo- and 16-bromo-estrogens and related compounds: Potential inhibitors for both estradiol 2- and 16α-hydroxylases in rat liver microsomes;Journal of Steroid Biochemistry;1989-07
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