口服康力龙 STANOZOLOL
口服康力龙，STANOZOLOL is an anabolic steroid(Genengin) derived from dihydrotestosterone. Each tablet contains 10 mg of stanozolol, micronized grade. It is designated chemically as 17-methyl-2’H -5α-androst-2eno[3,2-c]pyrazol-17β-ol.
Each tablet also contains lactose monohydrate, sodium starch glycolate, polyvidone 25,000, microcrystalline cellulose and magnesium stearate as excipients.
Stanozolol is an oral androgen derived from dihydrotestosterone. Stanozolol acts on androgen receptors to promote anabolism through increased nitrogen retention and protein synthesis in muscle tissue. Stanozolol is a strong anabolic substance with androgenic action. Stanozolol does not convert to estrogen and therefore does not produce typical estrogen mediated side effects such as water retention. Stanozolol has a large oral bioavailability, due to a C17 a-alkylation which allows the hormone to survive first pass liver metabolism. Stanozolol reduces SHBG increasing free testosterone levels.
Stanozolol
Molecular Formula: C22H36N2O
Molecular Weight: 344.53 gm/mol
Active life: 8 hours
Detection Time: 3 weeks
Anabolic/Androgenic Ratio (Range): 320:30
DESCRIPTION:
STANOZOLOL is an anabolic steroid derived from dihydrotestosterone. Each tablet contains 10 mg of stanozolol, micronized grade. It is designated chemically as 17-methyl-2’H -5α-androst-2eno[3,2-c]pyrazol-17β-ol.
Each tablet also contains lactose monohydrate, sodium starch glycolate, polyvidone 25,000, microcrystalline cellulose and magnesium stearate as excipients.
Stanozolol is an oral androgen derived from dihydrotestosterone. Stanozolol acts on androgen receptors to promote anabolism through increased nitrogen retention and protein synthesis in muscle tissue. Stanozolol is a strong anabolic substance with androgenic action. Stanozolol does not convert to estrogen and therefore does not produce typical estrogen mediated side effects such as water retention. Stanozolol has a large oral bioavailability, due to a C17 a-alkylation which allows the hormone to survive first pass liver metabolism. Stanozolol reduces SHBG increasing free testosterone levels.
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