Anodyne

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Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
Physical properties
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384.6 g/mol [1]
7 [1]
Structural Identifiers
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C25H36O3 [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] heptanoate [1]
CCCCCCC(=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/C25H36O3/c1-3-4-5-6-7-24(27)28-23-13-12-22-21-10-8-17-16-18(26)9-11-19(17)20(21)14-15-25(22,23)2/h9,11,16,20-23,26H,3-8,10,12-15H2,1-2H3/t20-,21-,22+,23+,25+/m1/s1 [1]
InChIKeyRFWTZQAOOLFXAY-BZDYCCQFSA-N [1]

Estradiol enantate

(Redirected from Estradiol enantate)

Estradiol enantate (also known as Estradiol enanthate, Estradiol Enantate, Estradiol 17-heptanoate, SQ 16,150, SQ-16150, SO-16150, SQ-16,150, RefChem:137916, 225-599-8 or Oestradiol 17-heptanoate) is a prodrug and estrogen substance of the steroid class.

Chemistry

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Estradiol enantate is a absolute mixture

Pharmacology

Estradiol enantate acts as a for:

Active metabolites
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Estradiol Generated by the Chemistry Development Kit (http://github.com/cdk)
Anodyne Usernotes
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0xea / Estradiol enantate via Subcutaneous and IntramuscularProdrug Ester of Estradiol; minor crashes when injected weekly; discomfort when injected every 4 days

See also []

  • Substituted steroids
  • Anodyne

    • External links []

    References []

    1. National Center for Biotechnology Information. PubChem Compound Summary for CID 21070, Estradiol enantate. Accessed September 15, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/21070

    2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Estradiol enantate. UNII: PAP315WZIA. Global Substance Registration System. Accessed September 15, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/PAP315WZIA