Identification of potent pyrazole based APELIN receptor (APJ) agonists.

Journal Article (Journal Article)

The apelinergic system comprises the apelin receptor and its cognate apelin and elabela peptide ligands of various lengths. This system has become an increasingly attractive target for pulmonary and cardiometabolic diseases. Small molecule regulators of this receptor with good drug-like properties are needed. Recently, we discovered a novel pyrazole based small molecule agonist 8 of the apelin receptor (EC50 = 21.5 µM, Ki = 5.2 µM) through focused screening which was further optimized to initial lead 9 (EC50 = 0.800 µM, Ki = 1.3 µM). In our efforts to synthesize more potent agonists and to explore the structural features important for apelin receptor agonism, we carried out structural modifications at N1 of the pyrazole core as well as the amino acid side-chain of 9. Systematic modifications at these two positions provided potent small molecule agonists exhibiting EC50 values of <100 nM. Recruitment of β-arrestin as a measure of desensitization potential of select compounds was also investigated. Functional selectivity was a feature of several compounds with a bias towards calcium mobilization over β-arrestin recruitment. These compounds may be suitable as tools for in vivo studies of apelin receptor function.

Full Text

Duke Authors

Cited Authors

  • Narayanan, S; Vasukuttan, V; Rajagopal, S; Maitra, R; Runyon, SP

Published Date

  • February 15, 2020

Published In

Volume / Issue

  • 28 / 4

Start / End Page

  • 115237 -

PubMed ID

  • 31948845

Pubmed Central ID

  • PMC7055011

Electronic International Standard Serial Number (EISSN)

  • 1464-3391

Digital Object Identifier (DOI)

  • 10.1016/j.bmc.2019.115237

Language

  • eng

Conference Location

  • England