Identification of novel azaindazole CCR1 antagonist clinical candidates

Bioorg Med Chem Lett. 2019 Feb 1;29(3):441-448. doi: 10.1016/j.bmcl.2018.12.024. Epub 2018 Dec 13.

Abstract

Exploring various cyclization strategies, using a submicromolar pyrazole HTS screening hit 6 as a starting point, a novel indazole based CCR1 antagonist core was discovered. This report presents the design and SAR of CCR1 indazole and azaindazole antagonists leading to the identification of three development compounds, including 19e that was advanced to early clinical trials.

Keywords: CCR1; Chemokine receptors; Clinical compound; Indazole; Scaffold hopping.

MeSH terms

  • Aza Compounds / chemical synthesis
  • Aza Compounds / chemistry
  • Aza Compounds / pharmacology*
  • Dose-Response Relationship, Drug
  • Drug Design
  • Humans
  • Indazoles / chemical synthesis
  • Indazoles / chemistry
  • Indazoles / pharmacology*
  • Molecular Structure
  • Receptors, CCR1 / antagonists & inhibitors*
  • Receptors, CCR1 / metabolism
  • Structure-Activity Relationship

Substances

  • Aza Compounds
  • CCR1 protein, human
  • Indazoles
  • Receptors, CCR1