Mestanolone
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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 |
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| Pregnancy cat. |
X(US) |
| Legal status | |
| Routes | Oral |
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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.
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.
Anabolic steroids (A14) (trademark names in brackets) | |
|---|---|
| Androstan (carbon 19 present) | Androstadienone • Boldenone undecylenate (Equipoise) • 4-Chlordehydromethyltestosterone (Turinabol) • Clostebol • Desoxymethyltestosterone (Madol) • DHEA • DHT • Drostanolone (Masteron) • Fluoxymesterone (Halotestin) • Furazabol (Miotolan) • Methandrostenolone (Dianabol) • Methenolone • Mesterolone (Proviron) • Methenolone enanthate (Primobolan) • Mestanolone • Norethandrolone • Oxandrolone (Anavar) • Oxymetholone (Anadrol) • Oxymetholone (Anadrol-50) • Quinbolone (Anabolicum Vister) • Stanozolol (Winstrol) • Testosterone |
| Estren (carbon 19 absent) | Ethylestrenol • Mibolerone (Cheque Drops) • Nandrolone (Deca Durabolin) • Norbolethone (Genabol) • Oxabolone cipionate • Tetrahydrogestrinone (The Clear) • Trenbolone (Fina) |
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