Chemistry:Testosterone benzoate
From HandWiki
Short description: Chemical compound
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| Other names | Testosterone 17β-benzoate; Androst-4-en-17β-ol-3-one 17β-benzoate |
| Routes of administration | Intramuscular injection |
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| Formula | C26H32O3 |
| Molar mass | 392.539 g·mol−1 |
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Testosterone benzoate, or testosterone 17β-benzoate, also known as androst-4-en-17β-ol-3-one 17β-benzoate, is a synthetic, injected anabolic–androgenic steroid (AAS) and an androgen ester – specifically, the benzoate C17β ester of testosterone – which was never marketed.[1][2] It is a prodrug of testosterone and, when administered via intramuscular injection, is associated with a long-lasting depot effect and extended duration of action.[3][4][5] The drug was first described in 1936 and was the first androgen ester and ester of testosterone to be synthesized.[6]
See also
References
- ↑ Handbook of Aqueous Solubility Data, Second Edition. CRC Press. 19 April 2016. pp. 1313–. ISBN 978-1-4398-0246-5. https://books.google.com/books?id=cfFzJFthLCIC&pg=PA1313.
- ↑ Behavioral Biology: Neuroendocrine Axis. Psychology Press. 5 September 2013. pp. 76–. ISBN 978-1-134-76125-8. https://books.google.com/books?id=NMTB6QB4VAYC&pg=PT76.
- ↑ CIBA Foundation Symposium (17 September 2009). Hormones, Psychology and Behaviour, Volume 3: Book I of Colloquia on Endocrinology. John Wiley & Sons. pp. 260–. ISBN 978-0-470-71486-7. https://books.google.com/books?id=gFc1uHEKxskC&pg=PA260.
- ↑ Natural Products in the Chemical Industry. Springer. 26 May 2015. pp. 540–. ISBN 978-3-642-54461-3. https://books.google.com/books?id=DbO4CQAAQBAJ&pg=PA540.
- ↑ CRC Handbook of Chromatography: Analysis and Characterization of Steroids. CRC Press. 21 August 1992. pp. 34–. ISBN 978-0-8493-3008-7. https://books.google.com/books?id=qQ9p1vnG-tMC&pg=PA34.
- ↑ "Increasing the Effectiveness of Testosterone". The Lancet 228 (5899): 674–676. 1936. doi:10.1016/S0140-6736(00)80929-0. ISSN 0140-6736.
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