Synthesis and receptor binding studies of some new arylcarboxamide derivatives as sigma-1 ligands

Bioorg Med Chem Lett. 2014 Feb 15;24(4):1021-5. doi: 10.1016/j.bmcl.2014.01.032. Epub 2014 Jan 20.

Abstract

We describe here the synthesis and the binding interaction with σ1 and σ2 receptors of a series of new arylcarboxamide derivatives variously substituted on the aromatic portions. Maintaining a partial scaffold of a series of compounds previously synthesized by us, we evaluate the effect of the substitution on σ binding. The synthesized compounds have been tested to estimate their affinity and selectivity toward σ1 and σ2 receptors. Two out of 16 derivatives showed an interesting σ1 affinity (21.2 and 13.6 nM-compounds 2m and 2p) and a good selectivity (Ki(σ2)/Ki(σ1) >140 and >40, respectively).

Keywords: Arylcarboxamide derivatives; Radioligand binding assays; σ-Receptors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amides / chemical synthesis
  • Amides / chemistry
  • Amides / pharmacology*
  • Animals
  • Binding Sites / drug effects
  • Dose-Response Relationship, Drug
  • Guinea Pigs
  • Ligands
  • Molecular Dynamics Simulation
  • Molecular Structure
  • Rats
  • Receptors, sigma / metabolism*
  • Sigma-1 Receptor
  • Structure-Activity Relationship

Substances

  • Amides
  • Ligands
  • Receptors, sigma
  • sigma-2 receptor