Mechanism of estrogen biosynthesis. Stereochemistry of C-1 hydrogen elimination in the aromatization of 2 beta-hydroxy-19-oxoandrostenedione.
Open Access
- 30 April 1981
- journal article
- research article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 256 (9) , 4472-4477
- https://doi.org/10.1016/s0021-9258(19)69459-7
Abstract
No abstract availableThis publication has 21 references indexed in Scilit:
- Aromatization of Δ-androstene-3,17-dione, 19-hydroxy-Δ4-androstene-3,17-dione, and 19-oxo-Δ-androstene-3,17-dione at a common catalytic site in human placental microsomesBiochemistry, 1977
- Participation of a Nonenzymatic Transformation in the Biosynthesis of Estrogens from AndrogensScience, 1977
- Synthesis of .beta.,.gamma.-acetylenic 3-oxo steroids of the 5,10-seco seriesThe Journal of Organic Chemistry, 1976
- Reassignment of the absolute configuration of 19-substituted 19-hydroxysteroids and stereomechanism of estrogen biosynthesisJournal of the American Chemical Society, 1975
- Conversion of an androgen epoxide into 17β-estradiol by human placental microsomesBiochemistry, 1975
- 3E. Steroid biosynthesis: Placenta 79. Mechanism of estrogen biosynthesisJournal of Steroid Biochemistry, 1974
- Formation of Steroids by the Pregnant Mare. III. Metabolism of 14C-Squalene and 3H-Dehydroisoandrosterone Injected into the Fetal Circulation1Endocrinology, 1973
- Stereochemistry of estrogen biosynthesisBiochemistry, 1969
- The Stereochemical Course of The Catalytic Hydrogenation of Ring a Unsaturated SteroidsJournal of the American Chemical Society, 1962
- Conversion of 19-hydroxy-Δ4-androstene-3,17-dione to estrone by endocrine tissueBiochimica et Biophysica Acta, 1955