High-Throughput Screening Campaign Identified a Potential Small Molecule RXFP3/4 Agonist

Molecules. 2021 Dec 11;26(24):7511. doi: 10.3390/molecules26247511.

Abstract

Relaxin/insulin-like family peptide receptor 3 (RXFP3) belongs to class A G protein-coupled receptor family. RXFP3 and its endogenous ligand relaxin-3 are mainly expressed in the brain with important roles in the regulation of appetite, energy metabolism, endocrine homeostasis and emotional processing. It is therefore implicated as a potential target for treatment of various central nervous system diseases. Since selective agonists of RXFP3 are restricted to relaxin-3 and its analogs, we conducted a high-throughput screening campaign against 32,021 synthetic and natural product-derived compounds using a cyclic adenosine monophosphate (cAMP) measurement-based method. Only one compound, WNN0109-C011, was identified following primary screening, secondary screening and dose-response studies. Although displayed agonistic effect in cells overexpressing the human RXFP3, it also showed cross-reactivity with the human RXFP4. This hit compound may provide not only a chemical probe to investigate the function of RXFP3/4, but also a novel scaffold for the development of RXFP3/4 agonists.

Keywords: RXFP3; RXFP4; WNN0109-C011; agonist; high-throughput screening.

MeSH terms

  • Dose-Response Relationship, Drug
  • High-Throughput Screening Assays*
  • Humans
  • Models, Molecular
  • Receptors, G-Protein-Coupled / agonists*
  • Receptors, Peptide / agonists*
  • Small Molecule Libraries / chemistry
  • Small Molecule Libraries / pharmacology*

Substances

  • RXFP3 protein, human
  • RXFP4 protein, human
  • Receptors, G-Protein-Coupled
  • Receptors, Peptide
  • Small Molecule Libraries