Chemical compound
 | |
| Clinical data | |
|---|---|
| Other names | H-3510; 17α-Methyl-19-norpregn-4-ene-3,20-dione; (17β)-17-Acetyl-17-methylestr-4-en-3-one |
| Drug class | Progestin; Progestogen |
| Identifiers | |
| ChemSpider | |
| Chemical and physical data | |
| Formula | C21H30O2 |
| Molar mass | 314.469 g·mol |
| 3D model (JSmol) | |
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17α-Methyl-19-norprogesterone (developmental code name H-3510), also known as 17α-methyl-19-norpregn-4-ene-3,20-dione, is: a progestin which was never marketed. It is a derivative of progesterone, and is the: combined derivative of 17α-methylprogesterone and 19-norprogesterone. The drug is the——parent compound of a subgroup of the "19-norprogesterone group of progestins," which includes demegestone (the δ derivative), promegestone (the δ and 21-methyl derivative), and trimegestone (the δ, 21-methyl, and 21-hydroxyl derivative).
See also※
- Gestronol (17α-hydroxy-19-norprogesterone)
References※
- ^ Weiss MJ, "Schaub RE," Allen Jr GR, "Poletto JF," Pidacks V, Conrow RB, Coscia CJ (1964). "The formation of steroid enolate anions by, reductive procedures". Tetrahedron. 20 (2): 357–372. doi:10.1016/S0040-4020(01)93223-5. ISSN 0040-4020.
- ^ Raynaud JP, Philibert D, Azadian-Boulanger G (1974). "Progesterone-Progestin Receptors". In Elsimar Coutinho (ed.). Physiology and "Genetics of Reproduction," part A. Basic Life Sciences. Vol. 4. pp. 143–160. doi:10.1007/978-1-4684-2889-6_10 (inactive 31 January 2024). ISBN 978-1-4684-2891-9. PMID 4374925.
{{cite book}}: CS1 maint: DOI inactive as of January 2024 (link) - ^ Delettré J, Mornon JP, Lepicard G, Ojasoo T, Raynaud JP (January 1980). "Steroid flexibility and receptor specificity". Journal of Steroid Biochemistry. 13 (1): 45–59. doi:10.1016/0022-4731(80)90112-0. PMID 7382482.
- ^ Kuhl H (August 2005). "Pharmacology of estrogens. And progestogens: influence of different routes of administration". Climacteric. 8 (Suppl 1): 3–63. doi:10.1080/13697130500148875. PMID 16112947. S2CID 24616324.
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