Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1224174 | Journal of Pharmaceutical and Biomedical Analysis | 2008 | 4 Pages |
Abstract
A new analogue of sildenafil was detected in a herbal aphrodisiac. The structure of the compound was established using LC–MS, UV and IR spectroscopy, MS–MS, and NMR. The compound, named thio-homosildenafil is a synthetic N-ethylpiperazine analogue of sildenafil in which also the CO moiety has been converted into a CS group. This is the first time a sildenafil analogue modified at the chromophore was identified as an adulterant of a herbal aphrodisiac. Preliminary pharmacological analysis confirmed the erectogenic potency of thio-homosildenafil.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Analytical Chemistry
Authors
B.J. Venhuis, G. Zomer, D. de Kaste,