Clometerone

Chemical compound
  • None
Identifiers
  • (6S,8S,9S,10R,13S,14S,16R,17S)-17-acetyl-6-chloro-10,13,16-trimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
CAS Number
  • 5591-27-5
PubChem CID
  • 14515731
ChemSpider
  • 16736897
UNII
  • 01L3E93T4C
CompTox Dashboard (EPA)
  • DTXSID20204508 Edit this at Wikidata
Chemical and physical dataFormulaC22H31ClO2Molar mass362.94 g·mol−13D model (JSmol)
  • Interactive image
  • C[C@@H]1C[C@H]2[C@@H]3C[C@@H](C4=CC(=O)CC[C@@]4([C@H]3CC[C@@]2([C@H]1C(=O)C)C)C)Cl
InChI
  • InChI=1S/C22H31ClO2/c1-12-9-17-15-11-19(23)18-10-14(25)5-7-21(18,3)16(15)6-8-22(17,4)20(12)13(2)24/h10,12,15-17,19-20H,5-9,11H2,1-4H3/t12-,15-,16+,17+,19+,20-,21-,22+/m1/s1
  • Key:UMRURYMAPMZKQO-NDKKBYRMSA-N

Clometerone (INNTooltip International Nonproprietary Name) (developmental code name L-38000), or clometherone (USANTooltip United States Adopted Name), also known as 6α-chloro-16α-methylprogesterone, is a synthetic pregnane steroid and derivative of progesterone which was reported in 1962 and is described as an antiestrogen and antiandrogen but was never marketed.[1][2][3]

Clometerone has been found to suppress estrone-induced uterine hypertrophy in mice at oral and parenteral doses in which progesterone is inactive (active at 10 µg with clometerone and progesterone inactive at 10–100 µg in the case of both routes).[2] However, its progestogenic potency in the Clauberg assay is considerably less than that of progesterone.[2] As such, the progestogenic effects of clometerone do not seem to parallel its estrogenic effects.[2] It was also studied as an antiandrogen in men but was found to slightly increase sebum production when given orally and to variably and inconsistently affect sebum production when given as a topical medication.[2]

See also

References

  1. ^ Elks J (14 November 2014). "Clometerone". The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 298–. ISBN 978-1-4757-2085-3.
  2. ^ a b c d e Rapala RT, Murray MJ (September 1962). "Disubstituted Progesterones. The 6,16-Chloro and Methyl Series". Journal of Medicinal and Pharmaceutical Chemistry. 91 (5): 1049–1053. doi:10.1021/jm01240a019. PMID 14056429.
  3. ^ Strauss JS, Pochi PE (1970). "Assay of anti-androgens in man by the sebaceous gland response". British Journal of Dermatology. 82 (s6): 33. doi:10.1111/j.1365-2133.1970.tb08003.x. ISSN 0007-0963. S2CID 73246983.
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SARMsTooltip Selective androgen receptor modulator
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Receptor/signaling modulators
Androgens and antiandrogens
Estrogen receptor modulators
Progesterone receptor modulators
List of androgens and anabolic steroids
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PRTooltip Progesterone receptor
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mPRTooltip Membrane progesterone receptor
(PAQRTooltip Progestin and adipoQ receptor)
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See also
Receptor/signaling modulators
Progestogens and antiprogestogens
Androgen receptor modulators
Estrogen receptor modulators
List of progestogens
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