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| Other names | Clometherone; L-38000; 6α-Chloro-16α-methylprogesterone; 6α-Chloro-16α-methylpregn-4-ene-3,20-dione |
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| Formula | C22H31ClO2 |
| Molar mass | 362.94 g·mol−1 |
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Clometerone (INN) (developmental code name L-38000), or clometherone (USAN), 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
- ^ 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.
- ^ 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.
- ^ 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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This page was last edited on 27 April 2024, at 17:41