Structural characterization of sulfoaildenafil,an analog of sildenafil |
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Authors: | Samuel R. Gratz Matthias Zeller Daryl W. Mincey Cheryl L. Flurer |
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Affiliation: | 1. U.S. Food and Drug Administration, Forensic Chemistry Center, 6751 Steger Drive, Cincinnati, OH 45237, USA;2. Department of Chemistry, Youngstown State University, One University Plaza, Youngstown, OH 44555, USA |
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Abstract: | Phosphodiesterase type 5 (PDE-5) inhibitors represent a class of drugs used primarily in the treatment of erectile dysfunction. Currently, three PDE-5 inhibitors have been approved by the U.S. Food and Drug Administration (FDA) for use in the United States: sildenafil citrate, tadalafil, and vardenafil hydrochloride trihydrate. A bulk material, labeled as an ingredient for a dietary supplement, was analyzed for the presence of PDE-5 inhibitors. The compound that was detected displayed structural similarities to sildenafil, and was characterized further using LC–MSn, FTICRMS, X-ray crystallography and NMR. The compound was given the name sulfoaildenafil. When compared to sildenafil, sulfoaildenafil contains a sulfur atom substitution for the oxygen atom in the pyrazolopyrimidine portion of the molecule, and a 3,5-dimethyl substitution on the piperazine ring, rather than the 4-methyl moiety. The X-ray crystallographic data indicate that the material in this sample is comprised of two polymorphs, which may affect the chemical and/or biological properties of any product formulated with this compound. |
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Keywords: | Sulfoaildenafil PDE-5 inhibitors Dietary supplement Liquid chromatography&ndash mass spectrometry (LC&ndash MS) Nuclear magnetic resonance (NMR) X-ray crystallography Accurate mass |
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