Development of high-affinity 5-HT3 receptor antagonists. 1. Initial structure-activity relationship of novel benzamides

Article abstract of DOI:10.1021/jm00083a014

This report describes the development of novel benzamides which are orally active, highly potent, specific antagonists of 5-HT₃ receptors. Described in this first report are the structure-activity relationships that led to novel structures with improved potency and selectivity. From this series of compounds, (S)-28 was identified and selected for further evaluation as a 5- HT₃ receptor antagonist. Compared with 5-HT₃ antagonists such as GR 38032F, BRL 43694, and metoclopramide, (S)-28 was most active in (a) inhibiting binding to 5-HT₃ receptor binding sites in rat entorhinal cortex with an K(i) value of 0.19 nM and (b) blocking cisplatin-induced emesis in the ferret with an ED₅₀ value determined to be 9 μg/kg po.