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Etamestrol

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Etamestrol
Identifiers
  • [(7R,8S,9S,13S,14S,17R)-1-benzoyloxy-17-ethynyl-17-hydroxy-7,13-dimethyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl] benzoate
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC35H34O5
Molar mass534.652 g·mol−1
3D model (JSmol)
  • CC1CC2=CC(=CC(=C2C3C1C4CCC(C4(CC3)C)(C#C)O)OC(=O)C5=CC=CC=C5)OC(=O)C6=CC=CC=C6
  • InChI=1S/C35H34O5/c1-4-35(38)18-16-28-30-22(2)19-25-20-26(39-32(36)23-11-7-5-8-12-23)21-29(31(25)27(30)15-17-34(28,35)3)40-33(37)24-13-9-6-10-14-24/h1,5-14,20-22,27-28,30,38H,15-19H2,2-3H3/t22-,27+,28+,30-,34+,35+/m1/s1
  • Key:FMEKKTLRKMEQKJ-RCJJHWPHSA-N

Etamestrol (INN; also known aseptamestrol and7α-methyl-19-nor-17α-pregna-1,3,5(10)-trien-20-yne-1,3,17-triol 1,3-dibenzoate; development codeZK-77992) is asynthetic,steroidalestrogen described as anovulation inhibitor (orhormonal contraceptive) that was synthesized in 1979 but was never marketed.[1]

References

[edit]
  1. ^Elks J (14 November 2014).The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 504–.ISBN 978-1-4757-2085-3.


ERTooltip Estrogen receptor
Agonists
Mixed
(SERMsTooltip Selective estrogen receptor modulators)
Antagonists
GPERTooltip G protein-coupled estrogen receptor
Agonists
Antagonists
Unknown


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