Estradiol dipropionate

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Estradiol dipropionate
Estradiol dipropionate.svg
Systematic (IUPAC) name
(17β)-estra-1,3,5(10)-triene-3,17-diyl dipropanoate
Clinical data
Legal status
  • ℞ (Prescription only)
Routes of
administration		 IM
Identifiers
CAS Number 113-38-2
ATC code None
PubChem CID: 8225
ChemSpider 7932
UNII NIG5418BXB YesY
ChEMBL CHEMBL1697791
Synonyms 17β-Estradiol-3,17-dipropionate
Chemical data
Formula C24H32O4
Molecular mass 384.509 g/mol
  • O=C(Oc1cc3c(cc1)[C@H]2CC[C@@]4([C@@H](OC(=O)CC)CC[C@H]4[C@@H]2CC3)C)CC
  • 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
  • Key:JQIYNMYZKRGDFK-RUFWAXPRSA-N

Estradiol dipropionate (BAN, JAN; brand names Agofollin, Diovocyclin, Progynon-DP, others) is a synthetic ester, specifically the 3,17-dipropanoyl ester, of the natural estrogen, estradiol.[1][2] Alongside estradiol benzoate, estradiol dipropionate was one of the first estradiol esters to be developed, having been patented in 1937,[3] and has been marketed since at least the 1940s.[4]

See also

References

  1. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  2. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  3. ↑ States2233025 United States 2233025, Karl Miescher, Riehen, & Caesar Scholz, "Estradiol-17-monoesters", published 1941-02-25, assigned to Ciba Pharmaceutical Products, Inc. 
  4. ↑ Lua error in package.lua at line 80: module 'strict' not found.



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