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Revision as of 05:16, 18 December 2016

Estradiol decanoate
Clinical data
Other namesE2D; Estradiol decylate; Estradiol 17β-decanoate; Estra-1,3,5(10)-triene-3,17β-diol 17β-decanoate
Identifiers
  • [(8R,9S,13S,14S,17S)-3-hydroxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl] decanoate
CAS Number
PubChem CID
ChemSpider
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC28H42O3
Molar mass426.641 g/mol g·mol−1
3D model (JSmol)
  • CCCCCCCCCC(=O)O[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CCC4=C3C=CC(=C4)O)C
  • InChI=1S/C28H42O3/c1-3-4-5-6-7-8-9-10-27(30)31-26-16-15-25-24-13-11-20-19-21(29)12-14-22(20)23(24)17-18-28(25,26)2/h12,14,19,23-26,29H,3-11,13,15-18H2,1-2H3/t23-,24-,25+,26+,28+/m1/s1
  • Key:YYFQNZXJGOTFRX-VMBLQBCYSA-N

Estradiol decanoate (E2D), or estradiol decylate, also known as estradiol 17β-decanoate or as estra-1,3,5(10)-triene-3,17β-diol 17β-decanoate, is a synthetic, steroidal estrogen and an estrogen ester – specifically, the 17β-decanoate diester of estradiol – which has been studied for use in hormone replacement therapy for ovariectomized women but was never marketed.[1][2]

See also

References

  1. ^ Luisi M, Kicovic PM, Alicicco E, Franchi F (1978). "Effects of estradiol decanoate in ovariectomized women". J. Endocrinol. Invest. 1 (2): 101–6. doi:10.1007/BF03350355. PMID 755846.
  2. ^ Ranjit Roy Chaudhury (1 January 1981). Pharmacology of Estrogens. Elsevier Science & Technology Books. p. 36. ISBN 978-0-08-026869-9.