Anodyne

EDP
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
Physical properties
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384.5 g/mol [1]
4.3 [1]
Structural Identifiers
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C24H32O4 [1]
[(8R,9S,13S,14S,17S)-13-methyl-3-propanoyloxy-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)OC(=O)CC)C [1]
InChI=1S/C24H32O4/c1-4-22(25)27-16-7-9-17-15(14-16)6-8-19-18(17)12-13-24(3)20(19)10-11-21(24)28-23(26)5-2/h7,9,14,18-21H,4-6,8,10-13H2,1-3H3/t18-,19-,20+,21+,24+/m1/s1 [1]
InChIKeyJQIYNMYZKRGDFK-RUFWAXPRSA-N [1]
Dosing
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Elimination half-lifeUnknown
Duration of actionIntramuscular injection (5 mg): 5 – 8 days

Estradiol dipropionate

(Redirected from Estradiol dipropionate)

Estradiol dipropionate (also known as Diprostron, Agofollin, Diovocylin, Progynon-DP, Akrofolline, Diovocyclin, Dimenformon dipropionate, Estroici, Estronex or Nacyclyl)

Chemistry

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Estradiol dipropionate is a absolute mixture

See also []

External links []

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 8225, Estradiol dipropionate. Accessed July 7, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/8225

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Estradiol dipropionate. UNII: NIG5418BXB. Global Substance Registration System. Accessed July 7, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/NIG5418BXB