Mestanolone
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| Please help improve this article or section by expanding it. Further information might be found on the talk page or at requests for expansion. (September 2007) |
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Mestanolone
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| Systematic (IUPAC) name | |
| (5S,8R,9S,10S,13S,14S,17S) -17-hydroxy-10,13,17-trimethyl-2,4,5,6,7,8,9,11,12,14,15, 16-dodecahydro-1H-cyclopenta[a]phenanthren-3-one | |
| Identifiers | |
| CAS number | |
| ATC code | ? |
| PubChem | |
| Chemical data | |
| Formula | C20H32O2 |
| Mol. mass | 304.467 g/mol |
| Pharmacokinetic data | |
| Bioavailability | 99% oral |
| Protein binding | yes |
| Metabolism | Hepatic |
| Half life | ? |
| Excretion | Renal |
| Therapeutic considerations | |
| Pregnancy cat. |
X(US) |
| Legal status | |
| Routes | Oral |
Mestanolone is the 17α-methylated version of dihydrotestosterone (DHT).[1] The systematic name of mestanolone is: 17β-hydroxy-17α-methylandrost-3-one.[2] It is an orally bioavailable androgenic steroid that is highly androgenic while only slightly anabolic. It is incapable of aromatization and is not an agonist of the progesterone receptor.
[edit] External links
was marketed as superdrol similar to anadrol50 and masteron
[edit] References
- ^ CTD (2007). Chemicals: mestanolone (English). CTD - Comparative Toxicogenomics Database. Retrieved on September 3, 2007.
- ^ Biology Online.org (2007). mestanolone (English). Biology Online.org. Retrieved on September 3, 2007.
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