Steroid structure and function—VI. The molecular conformation of 19-hydroxy-4-androstene-3,17-dione, as an intermediate for estrogen synthetase-Reference-Cited by-同舟云学术

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Steroid structure and function—VI. The molecular conformation of 19-hydroxy-4-androstene-3,17-dione, as an intermediate for estrogen synthetase

Published:1980-04 Issue:4 Volume:13 Page:383-386
ISSN:0022-4731
Container-title:Journal of Steroid Biochemistry
language:en
Short-container-title:Journal of Steroid Biochemistry

Author:

Duax William L.,Osawa Yoshio

Publisher

Elsevier BV

Subject

Endocrinology,Biochemistry

Reference18 articles.

1. Mechanism of aromatization;Osawa,1973

2. Inadequacy of the 19-aldehyde as an intermediate in estrogen biosynthesis;Osawa,1974

3. Mechanism of lyase reaction in androgen and estrogen biosynthesis;Osawa,1975

4. The biosynthesis of estrogens;Engel,1973

5. Identification by gas chromatography-mass spectrometry of intermediates in the aromatization of modified C19 steroids by human placental microsomes;Braselton;Steroids,1974

Cited by 22 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. Developing steroidal aromatase inhibitors-an effective armament to win the battle against breast cancer;European Journal of Medicinal Chemistry;2015-11

2. Aromatization of androstenedione and 16α-hydroxyandrostenedione in human placental microsomes;Steroids;2008-11

3. Mass spectrometric analysis of oxygenations in aromatization of androst-4-ene-3,6,17-trione, a suicide substrate of aromatase, by placental microsomes. Isotope effect and stereochemistry;The Journal of Steroid Biochemistry and Molecular Biology;2007-11

4. Stereochemistry of NaBH4 Reduction of a 19-Carbonyl Group of 3-Deoxy Androgens. Synthesis of [19S-3H]- and [19R-3H]-Labeled Aromatase Inhibitors Having a 19-Hydroxy Group;Chemical and Pharmaceutical Bulletin;2004

5. Probing the active site of aromatase with 2-methyl-substituted androstenedione analogs;Steroids;2003-08

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