What is stanozolol made up of?
Stanozolol is an orally active synthetic anabolic steroid and a 17alpha-alkylated derivative of dihydrotestosterone that is formed by the condensation of the 3-keto-aldehyde moiety of oxymetholone with hydrazine, with androgenic activity.
Is stanozolol water soluble?
Product Info
Cas No. | 10418-03-8 |
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Synonym | Strombia, Strombaject, Winstrol |
Melting Point | 229.8-242°C |
Solubility | Slightly soluble in water (1 mg/mL). Soluble in ethanol (24 mg/mL). |
Appearance | White Crystal Powder |
How long does stanozolol stay in your system?
Detection in body fluids The primary metabolites are unique to stanozolol and are detectable in the urine for up to 10 days after a single 5–10 mg oral dose.
When was stanozolol classified as a controlled substance?
In the United States, like other AAS, stanozolol is classified as a controlled substance under federal regulation; they were included as Schedule III controlled substances under the Anabolic Steroids Act, which was passed as part of the Crime Control Act of 1990.
Which is an active form of camp in Cilostazol?
Cilostazol is a selective inhibitor of phosphodiesterase type 3 (PDE3) with therapeutic focus on increasing cAMP. An increase in cAMP results in an increase in the active form of protein kinase A (PKA), which is directly related with an inhibition in platelet aggregation.
How is Cilostazol metabolized in the human body?
Cilostazol is metabolized by CYP3A4 and CYP2C19, two isoenzymes of the cytochrome P450 system. Drugs that inhibit CYP3A4, such as itraconazole, erythromycin, ketoconazole, and diltiazem, are known to interact with cilostazol.
Why was cycloastragenol banned from the market?
The U.S. Federal Trade Commission issued an order preventing TA Sciences from advertising products containing cycloastragenol as “anti-aging”. A single in vitro study on human CD4 and CD8 T cells led to claims that cycloastragenol may activate telomerase, leading to controversial claims for its role in reducing the effects of aging.