Mestanolone

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Mestanolone
File:Mestanolone.png
Systematic (IUPAC) name
(5α,17β)-17-hydroxy-17-methylandrostan-3-one
Clinical data
Pregnancy
category
  • US: X (Contraindicated)
Routes of
administration
Oral
Legal status
Legal status
Pharmacokinetic data
Bioavailability 99% oral
Protein binding yes
Metabolism Hepatic
Biological half-life ?
Excretion Renal
Identifiers
CAS Number 521-11-9
ATC code none
PubChem CID 10633
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
Molar mass 304.467 g/mol[[Script error: No such module "String".]]
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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.

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 phase's or when one wishes to avoid excess weight gain.

References

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de:Mestanolon
  1. CTD (2007). "Chemicals: mestanolone". CTD - Comparative Toxicogenomics Database. Retrieved September 3 2007.  Check date values in: |access-date= (help)
  2. Biology Online.org (2007). "mestanolone". Biology Online.org. Retrieved September 3 2007.  Check date values in: |access-date= (help)