The obligatory intermediacy of 16,17 alpha- and 16,17 beta-epoxides in the biotransformation of androsta-5,16-dien-3 beta-ol to androst-5-ene-3 beta, 16 alpha, 17 beta- and -3 beta, 16 beta, 17 alpha-triols by male rat liver microsomes.
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference36 articles.
1. Steroidal Free Radicals as Possible Intermediates in the Biosynthesis of C19- 16-Steroids
2. The intermediary role of 5-pregnene-3β,20β-diol in the biosynthesis of 16-unsaturated C19 steroids in boar testis
3. Formation of [17-2H]androsta-5,16-dien-3β-ol from [17,21,21,21]pregnenolone by the microsomal fraction of boar testis
4. The biosynthesis of some androst-16-enes from C21 and C19 steroids in boar testicular and adrenal tissue
5. Androgen Steroids as an Aid to the Detection of Oestrus in Pig Artificial Insemination
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. HISTORY OF DRUG METABOLISM RESEARCH IN JAPAN*;Drug Metabolism Reviews;2000-01
2. 16-ene-steroids in the human testis;The Journal of Steroid Biochemistry and Molecular Biology;1991-01
3. Epoxidation of androsta-5,16-dien-3 beta-ol by hepatic microsomal lipid peroxidation.;Journal of Biological Chemistry;1986-03
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