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Ethylestradiol

From Wikipedia, the free encyclopedia
Chemical compound
Not to be confused withEthinylestradiol orEthylestrenol.
Pharmaceutical compound
Ethylestradiol
Clinical data
Other names17α-Ethylestradiol; 17α-Ethylestra-1,3,5(10)-triene-3,17β-diol
Drug classEstrogen
Identifiers
  • (8R,9S,13S,14S,17S)-17-Ethyl-13-methyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthrene-3,17-diol
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC20H28O2
Molar mass300.442 g·mol−1
3D model (JSmol)
  • CC[C@@]1(CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CCC4=C3C=CC(=C4)O)C)O
  • InChI=1S/C20H28O2/c1-3-20(22)11-9-18-17-6-4-13-12-14(21)5-7-15(13)16(17)8-10-19(18,20)2/h5,7,12,16-18,21-22H,3-4,6,8-11H2,1-2H3/t16-,17-,18+,19+,20+/m1/s1
  • Key:GQHYKMYMSVJXJM-SLHNCBLASA-N

Ethylestradiol, or17α-ethylestradiol, also known as17α-ethylestra-1,3,5(10)-triene-3,17β-diol, is asyntheticestrogen which was never marketed. It occurs as anactive metabolite of theanabolic steroidsnorethandrolone andethylestrenol formed viaaromatase and is believed to be responsible for theestrogenic effects of norethandrolone and ethylestrenol.[1] The 3-methylether of ethylestradiol has been used as anintermediate in thesynthesis of certain19-nortestosteroneanabolic steroids,[2][3]Norethandrolone in particular.[4]

See also

[edit]

References

[edit]
  1. ^Llewellyn W (2011).Anabolics. Molecular Nutrition Llc. pp. 330–,591–598.ISBN 978-0-9828280-1-4.
  2. ^Fedorova OI, Pekarskaya ES, Lukashina IV, Grinenko GS (1974). "Synthesis of some derivatives op 19-nortestosterone from estra-1,3,5(10)-trienes".Pharmaceutical Chemistry Journal.8 (8):462–465.doi:10.1007/BF00757882.ISSN 0091-150X.S2CID 27243268.
  3. ^William Andrew Publishing (22 October 2013).Pharmaceutical Manufacturing Encyclopedia. Elsevier. pp. 1513–.ISBN 978-0-8155-1856-3.
  4. ^Colton FB, Nysted LN, Riegel B, Raymond AL (1957). "17-Alkyl-19-nortestosterones".Journal of the American Chemical Society.79 (5):1123–1127.Bibcode:1957JAChS..79.1123C.doi:10.1021/ja01562a028.ISSN 0002-7863.
ERTooltip Estrogen receptor
Agonists
Mixed
(SERMsTooltip Selective estrogen receptor modulators)
Antagonists
GPERTooltip G protein-coupled estrogen receptor
Agonists
Antagonists
Unknown
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