Bigmurph6
Banned
Prostanozol (demethylstanozolol tetrahydropyranyl)
Androgenic no data available
Anabolic no data available
Chemical Names
17beta-Hydroxy-5alpha-androstano
(3,2-c]pyrazole
Estrogenic Activity none
Progestational Activity no data available
Description
Prostanozol (demethylstanozolol THP) is an oral anabolic steroid closely related to Winstrol (stanozolol) in structure. It differs from stanozolol only by the removal of the C-17 alpha alkyl group, which undoubtedly hurts the oral bioavailability of this steroid. In an attempt to compensate for this, an ether group has been added. The ether increases oil solubility and the likelihood of lymphatic delivery with dietary fats, which bypass the first pass through the liver. This is the same principle on which Anabolicum Vister (quinbolone) was developed. In the case of Prostanozol, however, there is no oil carrier, which significantly lowers the chance for lymphatic delivery. This will necessitate a much higher oral dosage than would be needed otherwise. Among athletes, the drug is valued as a non-liver-toxic oral anabolic with properties qualitatively (although not quantitatively) similar to those of stanozolol.
Androgenic no data available
Anabolic no data available
Chemical Names
17beta-Hydroxy-5alpha-androstano
(3,2-c]pyrazole
Estrogenic Activity none
Progestational Activity no data available
Description
Prostanozol (demethylstanozolol THP) is an oral anabolic steroid closely related to Winstrol (stanozolol) in structure. It differs from stanozolol only by the removal of the C-17 alpha alkyl group, which undoubtedly hurts the oral bioavailability of this steroid. In an attempt to compensate for this, an ether group has been added. The ether increases oil solubility and the likelihood of lymphatic delivery with dietary fats, which bypass the first pass through the liver. This is the same principle on which Anabolicum Vister (quinbolone) was developed. In the case of Prostanozol, however, there is no oil carrier, which significantly lowers the chance for lymphatic delivery. This will necessitate a much higher oral dosage than would be needed otherwise. Among athletes, the drug is valued as a non-liver-toxic oral anabolic with properties qualitatively (although not quantitatively) similar to those of stanozolol.
