Discovery and pharmacological evaluation of a novel series of adamantyl cyanoguanidines as P2X7 receptor antagonists

Eur J Med Chem. 2017 Apr 21:130:433-439. doi: 10.1016/j.ejmech.2017.02.060. Epub 2017 Mar 2.

Abstract

Here we report adamantyl cyanoguanidine compounds based on hybrids of the adamantyl amide scaffold reported by AstraZeneca and cyanoguanidine scaffold reported by Abbott Laboratories. Compound 27 displayed five-fold greater inhibitory potency than the lead compound 2 in both pore-formation and interleukin-1β release assays, while 35-treated mice displayed an antidepressant phenotype in behavioral studies. This SAR study provides a proof of concept for hybrid compounds, which will help in the further development of P2X7R antagonists.

Keywords: ATP; Adamantane; Adamantyl; Alzheimer's; IL-1β; Inflammation; Neurodegenerative; P2X receptor; P2X(7)R antagonist.

MeSH terms

  • Adamantane / chemistry
  • Adamantane / pharmacology*
  • Animals
  • Antidepressive Agents / chemistry*
  • Antidepressive Agents / pharmacology
  • Behavior / drug effects
  • Drug Discovery
  • Guanidines / chemistry
  • Guanidines / pharmacology*
  • Mice
  • Purinergic P2X Receptor Antagonists / chemistry*
  • Purinergic P2X Receptor Antagonists / pharmacology
  • Structure-Activity Relationship

Substances

  • Antidepressive Agents
  • Guanidines
  • Purinergic P2X Receptor Antagonists
  • dicyandiamido
  • Adamantane