Etamestrol

Chemical 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
  • 73764-72-4
PubChem CID
  • 208935
ChemSpider
  • 181030
UNII
  • VM88TV4OS5
ChEMBL
  • ChEMBL2106046
CompTox Dashboard (EPA)
  • DTXSID70994669 Edit this at Wikidata
Chemical and physical data
FormulaC35H34O5
Molar mass534.652 g·mol−1
3D model (JSmol)
  • Interactive image
  • CC1CC2=CC(=CC(=C2C3C1C4CCC(C4(CC3)C)(C#C)O)OC(=O)C5=CC=CC=C5)OC(=O)C6=CC=CC=C6
InChI
  • 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) (developmental code name ZK-77992), or eptamestrol, also known as 7α-methyl-19-nor-17α-pregna-1,3,5(10)-trien-20-yne-1,3,17-triol 1,3-dibenzoate, is a synthetic, steroidal estrogen described as an ovulation inhibitor (or hormonal contraceptive) that was synthesized in 1979 but was never marketed.[1]

References

  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.


  • v
  • t
  • e
Estrogen receptor modulators
ERTooltip Estrogen receptor
Agonists
Mixed
(SERMsTooltip Selective estrogen receptor modulators)
Antagonists
  • Coregulator-binding modulators: ERX-11
GPERTooltip G protein-coupled estrogen receptor
Agonists
Antagonists
Unknown
See also
Receptor/signaling modulators
Estrogens and antiestrogens
Androgen receptor modulators
Progesterone receptor modulators
List of estrogens


Stub icon

This drug article relating to the genito-urinary system is a stub. You can help Wikipedia by expanding it.

  • v
  • t
  • e
Stub icon

This article about a steroid is a stub. You can help Wikipedia by expanding it.

  • v
  • t
  • e