Discovery of N-indanyl benzamides as potent RORγt inverse agonists

Eur J Med Chem. 2019 Apr 1:167:37-48. doi: 10.1016/j.ejmech.2019.01.082. Epub 2019 Feb 4.

Abstract

The retinoic acid receptor-related orphan receptor-gamma-t (RORγt) is a promising therapeutic target for treatment of Th17 cell-mediated autoimmune diseases. Based on a scaffold hopping/conformational restriction strategy, a series of N-indanyl benzamides as novel RORγt inverse agonists was discovered. Exploration of structure-activity relationship on the piperazine ring, benzoyl moiety and cyclopentyl moiety of N-indanyl benzamides 2a and 2d led to identification of potent RORγt inverse agonists. Compound 5c with (S)-enantiomer was found having an IC50 of 153.7 nM in Fluorescence Resonance Energy Transfer (FRET) assay, and an IC50 of 47.1 nM in mouse Th17 cell differentiation assay, which represents a promising starting point for developing potent small molecule RORγt inverse agonists. Binding modes of the two enantiomers 5c and 5d in RORγt ligand binding domain were also discussed.

Keywords: Autoimmune diseases; Binding modes; N-indanyl benzamides; RORγt inverse agonists; Th17 cells.

MeSH terms

  • Animals
  • Autoimmune Diseases / drug therapy
  • Benzamides / pharmacology*
  • Binding Sites
  • Cell Differentiation / drug effects
  • Drug Discovery*
  • Drug Inverse Agonism*
  • Fluorescence Resonance Energy Transfer
  • Indans / chemistry
  • Inhibitory Concentration 50
  • Mice
  • Nuclear Receptor Subfamily 1, Group F, Member 3 / agonists*
  • Stereoisomerism
  • Structure-Activity Relationship
  • Th17 Cells / cytology

Substances

  • Benzamides
  • Indans
  • Nuclear Receptor Subfamily 1, Group F, Member 3