4.6 Article

Isolation and structural characterization of a new tadalafil analog (chloropropanoylpretadalafil) found in a dietary supplement

Journal

JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS
Volume 128, Issue -, Pages 360-366

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jpba.2016.05.038

Keywords

Phosphodiesterase type-5 (PDE-5); inhibitors; New tadalafil analog; LC-HRAM-MS; GC/FT-IR/MS

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A screen for known PDE-5 inhibitors in a dietary supplement product marketed for enhanced sexual performance detected a compound that structurally resembled chloropretadalafil, a known analog of tadalafil. The compound was isolated from the supplement matrix using high performance liquid chromatography with ultraviolet detection (HPLC-UV) and a fraction collector, and was further characterized using gas chromatography with Fourier Transform infrared detection and mass spectral detection (GC/FT-IR/MS), as well as high resolution mass spectrometry (HRMS). The analog had an accurate mass of m/z 441.1216 (error is 0.8706 ppm) for the protonated species [M+H](+), corresponding to a molecular formula of C23H22ClN2O5. HRAM and GC/FT-IR/MS mass spectral fragmentation data suggested that the modification is a chloropropanoyl moiety extending from the nitrogen on the piperidine ring of chloropretadalafil. The proposed new analog has been named chloropropanoylpretadalafil. Published by Elsevier B.V.

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