Anodyne

EP
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
Physical properties
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328.4 g/mol [1]
5.1 [1]
Structural Identifiers
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C21H28O3 [1]
[(8R,9S,13S,14S,17S)-3-hydroxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl] propanoate [1]
CCC(=O)O[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CCC4=C3C=CC(=C4)O)C [1]
InChI=1S/C21H28O3/c1-3-20(23)24-19-9-8-18-17-6-4-13-12-14(22)5-7-15(13)16(17)10-11-21(18,19)2/h5,7,12,16-19,22H,3-4,6,8-11H2,1-2H3/t16-,17-,18+,19+,21+/m1/s1 [1]
InChIKeyPQCRZWCSVWBYSC-AGRFSFNASA-N [1]

Estradiol propionate

(Redirected from Estradiol propionate)

Estradiol propionate (also known as Estradiol 17-propionate, β-Estradiol 17-propionate, Estradiol17-Propionate, Estra-1,3,5(10)-triene-3,17-diol (17β)-, 17-propanoate, Ncgc00183033-01, (17β)-Estra-1,3,5(10)-triene-3,17-diol 17-Propanoate; Estradiol 17-Propionate 17β-Estradiol 17-Propionate; Akrofollin; Estradiol Propionate; Oestra-1,3,5(10)-trien-3,17β-diol 17-Propionate;, Estra-1,3,5(10)-triene-3,17β-diol 17-propionate, (1S,3aS,3bR,9bS,11aS)-7-hydroxy-11a-methyl-1H,2H,3H,3aH,3bH,4H,5H,9bH,10H,11H,11aH-cyclopenta[a]phenanthren-1-yl propanoate, Tox21_113447 or FE22825)

Chemistry

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Estradiol propionate is a absolute mixture

See also []

External links []

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 19571, Estradiol propionate. Accessed July 7, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/19571

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Estradiol propionate. UNII: K31PC34297. Global Substance Registration System. Accessed July 7, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/K31PC34297