Synthesis of 17β-[(1S)-1-hydroxy-2-propynyl]- and 17β-[(1R)-1-hydroxy-2-propynyl]androst-4--en-3-one. Potential suicide substrates of 20α- and 20β- hydroxysteroid dehydrogenases-Reference-Cited by-同舟云学术

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Synthesis of 17β-[(1S)-1-hydroxy-2-propynyl]- and 17β-[(1R)-1-hydroxy-2-propynyl]androst-4--en-3-one. Potential suicide substrates of 20α- and 20β- hydroxysteroid dehydrogenases

Published:1979-08 Issue:2 Volume:34 Page:199-206
ISSN:0039-128X
Container-title:Steroids
language:en
Short-container-title:Steroids

Author:

Covey Douglas F.

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Pharmacology,Endocrinology,Molecular Biology,Biochemistry

Reference8 articles.

1. The Synthesis of 20β,21-Dihydroxy-4-pregnen-3-one and 3,5-Pregnadiene-20β,21-diol*

2. Cardenolide analogs. 7. Synthesis and biological activity of some new steroidal guanylhydrazones

Cited by 10 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. 17 -Hydroxysteroid dehydrogenase: inhibitors and inhibitor design;Endocrine Related Cancer;1996-03-01

2. Mechanism Based Inhibition of Hydroxysteroid Dehydrogenases;Journal of Enzyme Inhibition;1991-01

3. Active-site directed inactivation of rat ovarian 20 α-hydroxysteroid dehydrogenase;Biochemical Journal;1986-12-15

4. Synthesis and characteristics of allylic 4-pregnene-3,20-diols found in gonadal and breast tissues;Steroids;1986-04

5. Inactivation of human placental 17 beta,20 alpha-hydroxysteroid dehydrogenase by 16-methylene estrone, an affinity alkylator enzymatically generated from 16-methylene estradiol-17 beta.;Journal of Biological Chemistry;1983-10

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