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

被引:9
作者
Kern, Sara E. [1 ]
Lorenz, Lisa M. [1 ]
Lanzarotta, Adam [1 ]
Nickum, Elisa A. [1 ]
Litzau, Jonathan J. [1 ]
机构
[1] US FDA, Forens Chem Ctr, Cincinnati, OH 45237 USA
关键词
Phosphodiesterase type-5 (PDE-5); inhibitors; New tadalafil analog; LC-HRAM-MS; GC/FT-IR/MS; SYNTHETIC PHOSPHODIESTERASE-5 INHIBITORS; PERFORMANCE LIQUID-CHROMATOGRAPHY; MASS-SPECTROMETRY; PDE-5; INHIBITORS; STRUCTURE ELUCIDATION; COUNTERFEIT PRODUCTS; ERECTILE DYSFUNCTION; IDENTIFICATION; SILDENAFIL; ADULTERANT;
D O I
10.1016/j.jpba.2016.05.038
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
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.
引用
收藏
页码:360 / 366
页数:7
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