- Mestanolone
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Mestanolone Systematic (IUPAC) name (5α,17β)-17-hydroxy-17-methylandrostan-3-one Clinical data AHFS/Drugs.com International Drug Names Pregnancy cat. X(US) Legal status DEA Schedule III (US) Routes Oral Pharmacokinetic data Bioavailability 99% oral Protein binding yes Metabolism Hepatic Half-life ? Excretion Renal Identifiers CAS number 521-11-9 ATC code None PubChem CID 10633 ChemSpider 10187 UNII S712YZ168E KEGG D01533 ChEMBL CHEMBL261514 Synonyms (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 Chemical data Formula C20H32O2 Mol. mass 304.467 g/mol SMILES eMolecules & PubChem (what is this?) (verify) 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.
Dosage Information
Dosages range from 10mg to 30mg a day for males. Women should avoid Mestanolone for it is very androgenic. Long term use, more than 12 weeks should be avoided do to hepatoxicity. Since Mestanolone is unable to convert to estrogen, it is very useful during cutting phases or when one wishes to avoid excess weight gain.References
- ^ CTD (2007). "Chemicals: mestanolone" (in English). CTD - Comparative Toxicogenomics Database. http://ctdbase.org/detail.go?type=chem&acc=C008376. Retrieved September 3 2007.
- ^ Biology Online.org (2007). "mestanolone" (in English). Biology Online.org. http://www.biology-online.org/dictionary/Mestanolone. Retrieved September 3 2007.
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