Chemistry:Clogestone acetate

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Short description: Chemical compound
Clogestone acetate
Clogestone acetate.svg
Clinical data
Other namesChlormadinol acetate; AY-11440; 3β,17α-Diacetoxy-6-chloropregna-4,6-diene-20-one
Drug classProgestogen; Progestogen ester
Identifiers
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEMBL
Chemical and physical data
FormulaC25H33ClO5
Molar mass448.98 g·mol−1
3D model (JSmol)

Clogestone acetate (USAN) (developmental code name AY-11440), also known as chlormadinol acetate or as 3β,17α-diacetoxy-6-chloropregna-4,6-diene-20-one,[1] is a steroidal progestin which was investigated as a progestin-only contraceptive and postcoital contraceptive but was never marketed.[2][3][4][5] It is the diacetate ester of clogestone, which, similarly was never marketed.[2] Clogestone acetate produces chlormadinone acetate as an active metabolite.[6]

See also

References

  1. Biochemical Actions of Hormones. Elsevier. 2 December 2012. pp. 323–. ISBN 978-0-323-15189-4. https://books.google.com/books?id=et3Lq-TitzAC&pg=PA323. 
  2. 2.0 2.1 The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. 14 November 2014. pp. 297–. ISBN 978-1-4757-2085-3. https://books.google.com/books?id=0vXTBwAAQBAJ&pg=PA297. 
  3. Human Fertility Control: Theory and Practice. Elsevier Science. 22 October 2013. pp. 3–. ISBN 978-1-4831-6361-1. https://books.google.com/books?id=1lL0AgAAQBAJ&pg=PA3. 
  4. "Contraception — retrospect and prospect". Progress in Drug Research, vol. 21. Progress in Drug Research / Fortschritte der Arzneimittelforschung / Progrès des rechersches pharmaceutiques. 21. Birkhäuser. 8 March 2013. pp. 293–407. doi:10.1007/978-3-0348-7098-6_4. ISBN 978-3-0348-7098-6. https://books.google.com/books?id=VFb2BwAAQBAJ&pg=PA321. 
  5. "[Clogestone acetate, a new orally effective progestagen]" (in de). Archiv Fur Gynakologie 209 (2): 136–148. August 1970. doi:10.1007/BF00668180. PMID 5537778. 
  6. "Measurement of serum clogestone acetate (AY-11,440) by a radioreceptor assay: a practical approach to the quantitative determination of synthetic progestins". The Journal of Clinical Endocrinology and Metabolism 40 (4): 728–731. April 1975. doi:10.1210/jcem-40-4-728. PMID 1127082.