Development of fluorinated CB(2) receptor agonists for PET studies

Bioorg Med Chem. 2013 Dec 1;21(23):7481-98. doi: 10.1016/j.bmc.2013.09.040. Epub 2013 Sep 24.

Abstract

A convergent strategy was followed to modify systematically carbazole based CB(2) receptor ligands. The length of the N-(fluoroalkyl) group (n in 7), the length of the alkanamide (m in 7) and the substitution pattern of the phenyl moiety (X and Y in 7) were varied systematically. The highest CB(2) affinity was found for the 2-fluoroethyl substituted carbazole derivative 20a (Ki=5.8nM) containing the propionamide and the 2-bromo-4-fluorophenyl moiety. According to docking studies 20a fits nicely into the binding pocket of the CB(2) receptor, but elongation of the fluoroethyl side chain leads to a different binding mode of the ligands. The high CB(2) affinity together with the high selectivity over the CB(2) subtype qualifies the fluoroethyl derivative 20a to be developed as a PET tracer.

Keywords: CB(2) receptor ligands; Carbazole derivatives; Docking; Fluorinated ligands; PET; Structure affinity relationships.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CHO Cells
  • Carbazoles / chemistry*
  • Carbazoles / pharmacology*
  • Cricetulus
  • Halogenation
  • Humans
  • Ligands
  • Molecular Docking Simulation
  • Positron-Emission Tomography
  • Receptor, Cannabinoid, CB2 / agonists*
  • Receptor, Cannabinoid, CB2 / metabolism*
  • Structure-Activity Relationship

Substances

  • Carbazoles
  • Ligands
  • Receptor, Cannabinoid, CB2
  • carbazole