Stanozolol C21H32N2O

Both salts were fully characterized by a variety of analytical methods, including single-crystal and powder X-ray diffraction (XRD), solid state NMR, differential scanning calorimetry (DSC) as well as dynamic vapour sorption (DVS). Though a similar functional group (OC–N–SO2) existed in SAC and AH, different annular R33(9) heterosynthons were observed for the two salts. The new salts are non-hygroscopic and resistant to STAN hydrate formation under high relative humidity (RH) conditions (95%). Additionally, dissolution studies indicate that the apparent solubilities and intrinsic dissolution rates (IDRs) of the salts are dramatically improved compared to those of pure STAN.

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• This medicine may be prescribed in case of anemia and hereditary type of angioedema.
• Calculated molecular properties are available for small molecules and natural products (not peptides).

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Stanozolol

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Protein kinase research chemicals

Background Owing to frequent administration of a wide range of pharmaceutical products, various environmental waters have been found to be contaminated with pharmacologically active substances. For example, stanozolol, a synthetic anabolic steroid, is frequently misused for performance enhancement as well as for illegal growth promoting purposes in veterinary practice. Previously we reported stanozolol in hair samples collected from subjects living in Budapest.

For this reason we initiated this study to explore possible environmental sources of steroid contamination. The aim of this study was to develop a method to monitor stanozolol in aqueous matrices using liquid chromatography tandem mass spectrometry (LC-MS/MS). Results Liquid-liquid extraction using pentane was found to be an efficient method for the extraction of stanozolol from water samples. The method was capable of detecting 0.25 pg/mL stanozolol when only 5 mL water was processed in the presence of stanozolol D3 as internal standard.