Potent antagonists of the CCR2b receptor. Part 3: SAR of the (R)-3-aminopyrrolidine series

Bioorg Med Chem Lett. 2008 Mar 15;18(6):1869-73. doi: 10.1016/j.bmcl.2008.02.015. Epub 2008 Feb 10.

Abstract

SAR studies were conducted around lead compound 1 using high-throughput parallel solution and solid phase synthesis. Our lead optimization efforts led to the identification of several CCR2b antagonists with potent activity in both binding and functional assays [Compound 71 CCR2b Binding IC(50) 3.2 nM; MCP-1-Induced Chemotaxis IC(50) 0.83 nM; Ca(2+) Flux IC(50) 7.5 nM].

MeSH terms

  • Calcium / metabolism
  • Cells, Cultured
  • Chemokine CCL2 / metabolism*
  • Chemotaxis / drug effects*
  • Chromatography, High Pressure Liquid
  • Fluorescence
  • Humans
  • Kidney / cytology
  • Kidney / drug effects
  • Kidney / metabolism
  • Molecular Structure
  • Monocytes / drug effects
  • Monocytes / metabolism
  • Pyrrolidines / chemical synthesis
  • Pyrrolidines / pharmacology*
  • Receptors, CCR2 / antagonists & inhibitors*
  • Receptors, CCR2 / metabolism
  • Structure-Activity Relationship
  • Transfection

Substances

  • CCL2 protein, human
  • CCR2 protein, human
  • Chemokine CCL2
  • Pyrrolidines
  • Receptors, CCR2
  • Calcium