Design, synthesis and structure-activity relationships of novel benzoxazolone derivatives as 18 kDa translocator protein (TSPO) ligands

Bioorg Med Chem. 2012 Sep 15;20(18):5568-82. doi: 10.1016/j.bmc.2012.07.023. Epub 2012 Jul 23.

Abstract

Selective 18 kDa translocator protein (TSPO) ligands are expected to be therapeutic agents with a wide spectrum of action on psychiatric disorders and fewer side effects. We designed novel benzoxazolone derivatives and examined the structure-activity relationship (SAR) of a series of compounds with various substituents at the amide part and C-5 position. Although a number of the synthesized compounds showed high TSPO binding affinity, these compounds had poor drug-like properties. Further optimization of pharmacokinetic properties of these compounds led to discovery of compound 74, which exhibited anxiolytic effect in the rat Vogel conflict model.

MeSH terms

  • Animals
  • Benzoxazoles / chemical synthesis*
  • Benzoxazoles / chemistry
  • Benzoxazoles / pharmacology*
  • Carrier Proteins / chemistry
  • Carrier Proteins / metabolism*
  • Dose-Response Relationship, Drug
  • Drug Design*
  • Ligands
  • Male
  • Molecular Structure
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, GABA-A / chemistry
  • Receptors, GABA-A / metabolism*
  • Structure-Activity Relationship

Substances

  • Benzoxazoles
  • Carrier Proteins
  • Ligands
  • Receptors, GABA-A
  • Tspo protein, rat
  • benzoxazolone