Current knowledge on the nucleotide agonists for the P2Y2 receptor

Bioorg Med Chem. 2018 Jan 15;26(2):366-375. doi: 10.1016/j.bmc.2017.11.043. Epub 2017 Dec 2.

Abstract

P2Y receptors are G-protein-coupled receptors (GPCRs) for extracellular nucleotides. There are eight mammalian P2Y receptor subtypes (P2Y1, P2Y2, P2Y4, P2Y6, P2Y11, P2Y12, P2Y13, and P2Y14). P2Y2 receptors are widely expressed and play important roles in multiple functionalities. Diquafosol tetrasodium, known as INS365, which was the first P2Y2 receptor agonists that had been approved in April 2010 and launched in Japan by Santen Pharmaceuticals. Besides, a series of similar agonists for the P2Y2 receptor are undergoing development to cure different diseases related to the P2Y2 receptor. This article illustrated the structure and functions of the P2Y2 receptor and focused on several kinds of agonists about their molecular structures, research progress and chemical synthesis methods. Last but not the least, we summarized the structures-activity relationship (SAR) of agonists for the P2Y2 receptor and expected more efficient agonists for the P2Y2 receptor.

Keywords: Agonist; Chemical synthesis; INS365; P2Y2 receptor; Structures-activity relationship.

Publication types

  • Review

MeSH terms

  • Dose-Response Relationship, Drug
  • Humans
  • Molecular Structure
  • Nucleotides / chemistry
  • Nucleotides / pharmacology*
  • Receptors, Purinergic P2Y2 / metabolism*
  • Structure-Activity Relationship

Substances

  • Nucleotides
  • Receptors, Purinergic P2Y2