Synthesis of functionalized derivatives of the gamma-secretase modulator BMS-932481 and identification of its major metabolite

Bioorg Med Chem Lett. 2020 Nov 15;30(22):127530. doi: 10.1016/j.bmcl.2020.127530. Epub 2020 Sep 2.

Abstract

In an effort to improve physical properties by introducing polar functionality into the bicyclic pyrimidine gamma-secretase modulator (GSM) clinical candidate BMS-932481, we prepared several oxidative products of BMS-932481. Among the analogs that were prepared, the C-5 alcohol 3 was identified as the predominant metabolite of BMS-932481 found in rat and human liver microsomes. Alcohol 3 was determined to be chemically unstable, leading to the hypothesis that 3 may lead to the production of reactive species both in vitro and in vivo.

Keywords: Alzheimer's disease; GS modulators; Metabolites.

MeSH terms

  • Amyloid Precursor Protein Secretases / metabolism*
  • Aniline Compounds / chemistry
  • Aniline Compounds / metabolism
  • Aniline Compounds / pharmacology*
  • Animals
  • Dose-Response Relationship, Drug
  • Humans
  • Microsomes, Liver / chemistry
  • Microsomes, Liver / metabolism
  • Molecular Structure
  • Pyrimidines / chemistry
  • Pyrimidines / metabolism
  • Pyrimidines / pharmacology*
  • Rats
  • Structure-Activity Relationship

Substances

  • 7-(4-fluorophenyl)-N2-(3-methoxy-4-(3-methyl-1H-1,2,4-triazol-1-yl)phenyl)-N4-methyl-6,7-dihydro-5H-cyclopenta(d)pyrimidine-2,4-diamine
  • Aniline Compounds
  • Pyrimidines
  • Amyloid Precursor Protein Secretases