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Mesterolone (Proviron)

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by Bill Roberts - Proviron, an anabolic steroid, is particularly interesting. I suspect that it not only acts as an antiaromatase but in an unknown DHT-like anti-estrogenic manner. This might involve estrogen receptor downregulation for example. In any case, aromatase inhibition and/or Clomid don’t seem to give the same effect on appearance and muscle hardness as when Proviron is included.

This drug has good binding to the androgen receptor, but in muscle tissue most of it never reaches the androgen receptor because it is enzymatically converted to the diol. Thus, it is not an effective anabolic. It is somewhat effective as an anti-gyno agent, however, and appears to reduce estrogenic bloating if that problem exists.

Proviron reduces either levels of estrogen or the effect of estrogen. Thus, it is useful for avoiding gynecomastia, although it probably should not be relied upon as the sole drug for that. It is not hepatotoxic. It has the usual side effects of anabolic/androgenic steroids, with the added effect that it is particularly prone to cause erections.

Mesterolone is the chemical name of active ingredient in Proviron. Proviron was a registered trademark of Schering AG in the United States and/or other countries prior to cancellation.

Proviron Resources

Proviron Pictures

Proviron (mesterolone) Pictures and Photographs

Mesterolone (Proviron) Chemical Structure

Substance name

Mesterolone [USAN]
Chemical name Androstan-3-one, 17-hydroxy-1-methyl-, (1alpha,5alpha,17beta)-
Systematic name IUPAC: (1S,5S,8R,9S,10R,13S,14S,17S)-17-hydroxy-1,10,13-trimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one
CAS number 1424-00-6
Merck Index Number Merck 11, 5817
Chemical formula C20-H32-O2
Molecular weight 304.467 g/mol
Bioavailability  
Metabolism Hepatic
Elimination half-life ?
Excretion Urinary: 90%; Fecal: 6%
Pregnancy category X
Legal status Illegal (US); DEA Schedule III (US)
Routes of administration Oral

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