Chemistry:Stenbolone
From HandWiki
Short description: Chemical compound
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| Other names | 2-Methyl-5α-androst-1-en-17β-ol-3-one; 2-Methyl-δ1-4,5α-dihydrotestosterone; 2-Methyl-δ1-DHT; Deacetylanatrofin |
| Routes of administration | Intramuscular injection (as stenbolone acetate) |
| Drug class | Androgen; Anabolic steroid |
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| Formula | C20H30O2 |
| Molar mass | 302.458 g·mol−1 |
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Stenbolone is an anabolic–androgenic steroid (AAS) of the dihydrotestosterone (DHT) group which was never marketed.[1][2][3][4] A C17β ester prodrug of stenbolone, stenbolone acetate, is used as an AAS for depot intramuscular injection under the brand names Anatrofin and Stenobolone.[1][3]
Chemistry
Stenbolone, also known as 2-methyl-δ1-4,5α-dihydrotestosterone (2-methyl-δ1-DHT) or as 2-methyl-5α-androst-1-en-17β-ol-3-one, is a synthetic androstane steroid and a derivative of DHT.[1][3] It is closely related structurally to drostanolone (2-methyl-DHT), 1-testosterone (δ1-DHT), and methylstenbolone (17α-methylstenbolone).[5]
Society and culture
Generic names
Stenbolone is the generic name of the drug and its INN.[1][3][4]
References
- ↑ 1.0 1.1 1.2 1.3 The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. 14 November 2014. pp. 1–. ISBN 978-1-4757-2085-3. https://books.google.com/books?id=0vXTBwAAQBAJ&pg=RA1-PA263.
- ↑ William Llewellyn (2011). Anabolics. Molecular Nutrition Llc. pp. 301–. ISBN 978-0-9828280-1-4. https://books.google.com/books?id=afKLA-6wW0oC&pg=PT301.
- ↑ 3.0 3.1 3.2 3.3 Index Nominum 2000: International Drug Directory. Taylor & Francis. January 2000. pp. 962–. ISBN 978-3-88763-075-1. https://books.google.com/books?id=5GpcTQD_L2oC&pg=PA962.
- ↑ 4.0 4.1 Concise Dictionary of Pharmacological Agents: Properties and Synonyms. Springer Science & Business Media. 6 December 2012. pp. 261–. ISBN 978-94-011-4439-1. https://books.google.com/books?id=tsjrCAAAQBAJ&pg=PA261.
- ↑ "Designer steroids - over-the-counter supplements and their androgenic component: review of an increasing problem". Andrology 3 (2): 150–5. 2015. doi:10.1111/andr.307. PMID 25684733.
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