Estradiol dienantate

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Estradiol dienantate
Clinical data
Other namesEstradiol dienantate
Routes of
administration		Intramuscular injection
Identifiers
  • (3-heptanoyloxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl) heptanoate
CAS Number
PubChem CID
ChemSpider
UNII
ECHA InfoCard100.028.903 Edit this at Wikidata
Chemical and physical data
FormulaC32H48O4
Molar mass496.72112 g/mol g·mol−1
3D model (JSmol)
  • CCCCCCC(=O)OC1CCC2C1(CCC3C2CCC4=C3C=CC(=C4)OC(=O)CCCCCC)C
  • InChI=1S/C32H48O4/c1-4-6-8-10-12-30(33)35-24-15-17-25-23(22-24)14-16-27-26(25)20-21-32(3)28(27)18-19-29(32)36-31(34)13-11-9-7-5-2/h15,17,22,26-29H,4-14,16,18-21H2,1-3H3
  • Key:OVAHZPTYWMWNKO-UHFFFAOYSA-N

Estradiol dienanthate, or estradiol 3,17-dihepanoate, is a semisynthetic, steroidal estrogen.[1] It is an estrogen ester, specifically, and an ester of estradiol.[1] The drug is a component of Climacteron, an injectable combination formulation of testosterone enanthate, estradiol dienanthate, and estradiol benzoate that is used in the treatment of menopausal symptoms in women.[2][3][4]

See also

References

  1. ^ a b J. Elks (14 November 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. p. 898. ISBN 978-1-4757-2085-3.
  2. ^ Ginsburg, Elizabeth S. (1999). "Androgen Replacement in Postmenopausal Women". 18: 209–219. doi:10.1007/978-1-59259-246-3_13. {{cite journal}}: Cite journal requires |journal= (help)
  3. ^ Robert B. Greenblatt; William E. Barfield; Edwin C. Jungck (January 1962). "The treatment of the menopause". Can Med Assoc J. 86 (3): 113–4. PMC 1848811. PMID 13901504.
  4. ^ David B. Seifer (27 July 1999). Menopause: Endocrinology and Management. Springer Science & Business Media. pp. 183–. doi:10.1007/978-1-59259-246-3. ISBN 978-1-59259-246-3.



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