Novel 4-phenylpiperidine-2,6-dione derivatives. Ligands for α 1-adrenoceptor subtypes

Abstract

A number of new 4-phenylpiperidine-2,6-diones bearing at the 1-position an ω-[4-(substituted phenyl)piperazin-1-yl]alkyl moiety were designed and synthesized as ligands for the α 1-adrenergic receptor (α 1-AR) subtypes. Some synthesized compounds, tested in binding assays for the human cloned α 1A-, α 1B-, and α 1D-AR subtypes, displayed affinities in the nanomolar range. Highest affinity values were found in derivatives having a butyl connecting chain between the 4-phenylpiperidine-2,6-dione and the phenylpiperazinyl moieties. 1-[4-[4-(2-Methoxyphenyl)piperazin-1-yl]butyl]-4-phenylpiperidine-2,6-dione ( 34) showed the best affinity for the α 1A-AR (p K i = 8.74) and 10-fold selectivity compared to the other two α 1-AR subtypes. Some representative compounds were also tested in order to evaluate their effects on the signal transduction pathway coupled to α 1-AR subtypes. They all blocked norepinephrine-induced stimulation of inositol phospholipid hydrolysis, thus behaving as antagonists. Binding data were used to refine a previously developed pharmacophoric model for α 1D-ARs. The revised model shows a highly predictive power and could be useful for the future design of high affinity α 1D-AR ligands.