Mestanolone

Mestanolone
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 N
ATC code None
PubChem CID 10633
ChemSpider 10187 YesY
UNII S712YZ168E YesY
KEGG D01533 YesY
ChEMBL CHEMBL261514 YesY
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
 N(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

  1. ^ CTD (2007). "Chemicals: mestanolone" (in English). CTD - Comparative Toxicogenomics Database. http://ctdbase.org/detail.go?type=chem&acc=C008376. Retrieved September 3 2007. 
  2. ^ Biology Online.org (2007). "mestanolone" (in English). Biology Online.org. http://www.biology-online.org/dictionary/Mestanolone. Retrieved September 3 2007.