Steroid structure and function I. Conformational transmission in 17α-acetoxy progesterone
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Clinical Biochemistry,Pharmacology,Endocrinology,Molecular Biology,Biochemistry
Reference17 articles.
1. Affinities of progestogen and estrogen receptors in rabbit uterus for synthetic progestogens
2. Atlas of Steroid Structure;Duax,1975
3. Structure cristalline et moléculaire de la progestérone, C21H30O2
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1. The regio- and stereo-selective reduction of steroidal 4-en-3-ones using Na2S2O4/NaHCO3 and CuCl/NaBH4;Steroids;2013-12
2. Transformation of structurally diverse steroidal analogues by the fungus Corynespora cassiicola CBS 161.60 results in generation of 8β-monohydroxylated metabolites with evidence in favour of 8β-hydroxylation through inverted binding in the 9α-hydroxylase;Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids;2011-12
3. Conformational Studies on (17α,20Z)-21-(X-Phenyl)-19-norpregna-1,3,5(10),20-tetraene-3,17β-diols Using 1D and 2D NMR Spectroscopy and GIAO Calculations of 13C Shieldings;The Journal of Organic Chemistry;2000-10-13
4. Nomegestrol acetate, a clinically useful 19-norprogesterone derivative which lacks estrogenic activity;The Journal of Steroid Biochemistry and Molecular Biology;1995-11
5. Ring a conformation in steroids. 3—Cyclosteroids and cyclopropanosteroids;Magnetic Resonance in Chemistry;1995-07
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