Extensive rigid analogue design maps the binding conformation of potent N -benzylphenethylamine 5-HT2A serotonin receptor agonist ligands

Abstract

Based on the structure of the superpotent 5-HT2A agonist 2-(4-bromo-2,5-dimethoxyphenyl)-N-[(2-methoxyphenyl)methyl]ethanamine, which consists of a ring-substituted phenethylamine skeleton modified with an N-benzyl group, we designed and synthesized a small library of constrained analogues to identify the optimal arrangement of the pharmacophoric elements of the ligand. Structures consisted of diversely substituted tetrahydroisoquinolines, piperidines, and one benzazepine. Based on the structure of (S,S)-9b, which showed the highest affinity of the series, we propose an optimal binding conformation. (S,S)-9b also displayed 124-fold selectivity for the 5-HT 2A over the 5-HT2C receptor, making it the most selective 5-HT2A receptor agonist ligand currently known. © 2012 American Chemical Society.