Propetandrol
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| Clinical data | |
|---|---|
| Trade names | Solevar |
| Identifiers | |
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| Synonyms | Propethandrol; SC-7294; 3β-(Propionyloxy)-17α-ethylestr-4-en-17β-ol; 17α-Ethylestr-4-en-3β,17β-diol 3β-propionate; 17α-Ethyl-19-nortestosterone 3β-propionate; 19-Nor-17α-pregn-4-ene-3β,17β-diol 3β-propionate; Norethandrolone 3β-propionate |
| CAS Number |
3638-82-2 |
| PubChem (CID) | 20055548 |
| ChemSpider |
16737110 |
| UNII |
K0H1J6311W |
| ChEMBL | CHEMBL2105236 |
| Chemical and physical data | |
| Formula | C23H36O3 |
| Molar mass | 360.53 g/mol |
| 3D model (Jmol) | Interactive image |
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Propetandrol (INN) (brand name Solevar; former developmental code name SC-7294), or propethandrol, also known as 17α-ethyl-19-nortestosterone 3β-propionate or 17α-ethyl-19-nor-4-androstenediol 3β-propionate, as well as 17α-ethylestr-4-en-3β,17β-diol 3β-propionate, is a synthetic, orally active anabolic-androgenic steroid (AAS) and progestogen and a 17α-alkylated derivative of 19-nortestosterone.[1][2] It is an androgen ester – specifically, the 3β-propionate ester of norethandrolone (17α-ethyl-19-nortestosterone).[1][2]
See also
References
- 1 2 J. Elks (14 November 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. p. 1031. ISBN 978-1-4757-2085-3.
- 1 2 GELLER J (1962). "Effect of 17-ethyl-19-nortestosterone 3-enol propionate (SC-7294) on the metabolism of adrenal cortical steroids". J. Clin. Endocrinol. Metab. 22: 1116–21. doi:10.1210/jcem-22-11-1116. PMID 13947091.
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See also: Androgens and antiandrogens • Estrogens and antiestrogens • Glucocorticoids and antiglucocorticoids • Mineralocorticoids and antimineralocorticoids • Gonadotropins and GnRH | |||||||||||||||||||||||||||||||
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See also: Estrogenics • Glucocorticoidics • Mineralocorticoidics • Progestogenics • Steroid hormone metabolism modulators • List of androgens/anabolic steroids | |||||||||||
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See also: Androgenics • Estrogenics • Glucocorticoidics • Mineralocorticoidics • Steroid hormone metabolism modulators | |||||||||||
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