Discovery of small molecule agonists targeting neuropeptide Y4 receptor using homology modeling and virtual screening

Chem Biol Drug Des. 2019 Dec;94(6):2064-2072. doi: 10.1111/cbdd.13611. Epub 2019 Sep 12.

Abstract

Neuropeptide Y4 receptor has the most significant effect on body weight and fat mass in its physiological functions, and the activation of Y4 receptor has explicit role on losing weight. The Y4 receptor has been successfully applied in the development of anti-obesity agent, thus representing a potential therapeutic target for obesity treatment. Here, we reported the first discovery of small molecule agonists targeting Y4 receptor: three Y4 receptor models with active and inactive conformations were built, each model was submitted following structure-based virtual screening, and finally six hits were identified as Y4 receptor agonists. These results confirm the reliability of the constructed Y4 receptor models and the proposed computational strategy for investigating novel Y4 receptor agonists. These new small molecule Y4 receptor agonists will contribute to the further development of Y4 agonists as potential therapeutics and functional probes.

Keywords: Y4 receptor; agonist; conformational state; docking; homology modeling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Benzene / chemistry
  • Binding Sites
  • Databases, Chemical
  • Drug Discovery
  • Humans
  • Molecular Docking Simulation
  • Protein Structure, Tertiary
  • Receptors, Neuropeptide Y / agonists*
  • Receptors, Neuropeptide Y / metabolism
  • Small Molecule Libraries / chemistry*
  • Small Molecule Libraries / metabolism

Substances

  • Receptors, Neuropeptide Y
  • Small Molecule Libraries
  • neuropeptide Y4 receptor
  • Benzene