Pyrrolinone derivatives as a new class of P2X3 receptor antagonists Part 2: Discovery of orally bioavailable compounds

Bioorg Med Chem Lett. 2019 Mar 1;29(5):688-693. doi: 10.1016/j.bmcl.2019.01.039. Epub 2019 Feb 1.

Abstract

Some P2X3 receptor antagonists have been developed as new therapeutic drugs for pain. We discovered a novel chemotype of P2X3 receptor antagonists with a pyrrolinone skeleton. Because of SAR studies to improve bioavailability of lead compound 2, compound (R)-24 was identified, which showed an analgesic effect against neuropathic pain by oral administration. We constructed a human P2X3 homology model as a template for the zebrafish P2X4 receptor, which agreed with SAR studies of pyrrolinone derivatives.

Keywords: Ion channels; P2X3 receptor antagonists; Pain; Purinergic receptors; Pyrrolinone derivatives.

MeSH terms

  • Administration, Oral
  • Biological Availability
  • Drug Discovery
  • High-Throughput Screening Assays
  • Humans
  • Inhibitory Concentration 50
  • Neuralgia / drug therapy
  • Purinergic P2X Receptor Antagonists / administration & dosage
  • Purinergic P2X Receptor Antagonists / pharmacokinetics
  • Purinergic P2X Receptor Antagonists / pharmacology*
  • Purinergic P2X Receptor Antagonists / therapeutic use
  • Pyrroles / pharmacology*
  • Receptors, Purinergic P2X3 / drug effects*
  • Structure-Activity Relationship

Substances

  • Purinergic P2X Receptor Antagonists
  • Pyrroles
  • Receptors, Purinergic P2X3