Synthesis of (3-hydroxy-pyrazolin-5-yl)glycine based ligands interacting with ionotropic glutamate receptors

Eur J Med Chem. 2014 Mar 21:75:151-8. doi: 10.1016/j.ejmech.2014.01.029. Epub 2014 Jan 25.

Abstract

Following the concept that increasing the molecular complexity may enhance the receptor selectivity, we replaced the 3-hydroxy-isoxazoline ring of model compound tricholomic acid with a 3-hydroxy-pyrazoline ring, which could be variously decorated at the N1 position, inserting groups characterized by different electronic and steric properties. Binding assays on rat brain synaptic membranes showed that, depending on the nature of the substituent, some of the new synthesized ligands interacted with either AMPA or KA receptors, with affinities in the mid-micromolar range.

Keywords: Excitatory amino acid transporters; Ionotropic glutamate receptors; Pyrazoline; l-Glutamic acid.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain / drug effects
  • Brain / metabolism
  • Glycine / analogs & derivatives*
  • Glycine / chemical synthesis
  • Glycine / chemistry
  • Glycine / pharmacology
  • Isoxazoles / chemical synthesis
  • Isoxazoles / chemistry*
  • Isoxazoles / pharmacology*
  • Ligands
  • Pyrazoles / chemical synthesis
  • Pyrazoles / chemistry*
  • Pyrazoles / pharmacology*
  • Rats
  • Receptors, Ionotropic Glutamate / metabolism*
  • Receptors, Kainic Acid / metabolism

Substances

  • Isoxazoles
  • Ligands
  • Pyrazoles
  • Receptors, Ionotropic Glutamate
  • Receptors, Kainic Acid
  • tricholomic acid
  • Glycine