Design, synthesis, and biological evaluation of fluorinated imidazo[1,2-a]pyridine derivatives with potential antipsychotic activity

Eur J Med Chem. 2016 Nov 29:124:456-467. doi: 10.1016/j.ejmech.2016.08.059. Epub 2016 Aug 26.

Abstract

Based on our recent finding that α1 selective GABA-A receptor potentiator-zolpidem-(a hypnotic drug) exerts antipsychotic-like effects in rats, we developed a series of fluorinated imidazo[1,2-a]pyridine derivatives as potential novel antipsychotic agents. The selected compounds displayed high affinity and positive allosteric modulator properties at the GABA-A receptor, enhanced metabolic stability and lack of hepatotoxicity. The most promising compound 2-(2-(4-fluorophenyl)-6-methylimidazo[1,2-a]pyridin-3-yl)-N,N-dimethylethanamide (26) showed antipsychotic-like activity in amphetamine-induced hyperlocomotion test in rats (MED = 1 mg/kg) and was characterized by a longer duration of antipsychotic-like activity as compared to zolpidem. These results are an encouraging example of a compound with non-dopaminergic mechanism of action displaying antipsychotic activity and are a point of entry for the future studies in this field.

Keywords: Imidazo[1,2-a]pyridine; Positive allosteric modulators of GABA-A receptor; Psychosis; Schizophrenia; Zolpidem.

MeSH terms

  • Allosteric Regulation / drug effects
  • Animals
  • Antipsychotic Agents / chemical synthesis*
  • Antipsychotic Agents / chemistry
  • Antipsychotic Agents / pharmacology*
  • Antipsychotic Agents / toxicity
  • Binding Sites
  • Cell Survival / drug effects
  • Chemistry Techniques, Synthetic
  • Drug Design*
  • Electrophysiological Phenomena / drug effects
  • Halogenation*
  • Hep G2 Cells
  • Humans
  • Pyridines / chemical synthesis*
  • Pyridines / chemistry
  • Pyridines / pharmacology*
  • Pyridines / toxicity
  • Rats
  • Receptors, GABA-A / chemistry
  • Receptors, GABA-A / metabolism

Substances

  • Antipsychotic Agents
  • Pyridines
  • Receptors, GABA-A