Tetrahydropyrazolo[4,3-c]pyridine derivatives as potent and peripherally selective cannabinoid-1 (CB1) receptor inverse agonists

Bioorg Med Chem Lett. 2016 Nov 15;26(22):5597-5601. doi: 10.1016/j.bmcl.2016.09.026. Epub 2016 Sep 12.

Abstract

Peripherally restricted CB1 receptor inverse agonists hold potential as useful therapeutics to treat obesity and related metabolic diseases without causing undesired CNS-mediated adverse effects. We identified a series of tetrahydropyrazolo[4,3-c]pyridine derivatives as potent and highly peripherally selective CB1 receptor inverse agonists. This discovery was achieved by introducing polar functional groups into the molecule, which increase the topological polar surface area and reduce its brain-penetrating ability.

Keywords: CB1 receptor; Cannabinoid receptor; Inverse agonist; Peripheral selectivity; Peripherally restricted.

MeSH terms

  • Animals
  • Brain / drug effects
  • Brain / metabolism
  • Cannabinoid Receptor Antagonists / chemistry*
  • Cannabinoid Receptor Antagonists / pharmacokinetics
  • Cannabinoid Receptor Antagonists / pharmacology*
  • Drug Inverse Agonism
  • Humans
  • Male
  • Mice, Inbred C57BL
  • Obesity / drug therapy
  • Obesity / metabolism
  • Pyrazoles / chemistry
  • Pyrazoles / pharmacokinetics
  • Pyrazoles / pharmacology
  • Pyridines / chemistry*
  • Pyridines / pharmacokinetics
  • Pyridines / pharmacology*
  • Receptor, Cannabinoid, CB1 / antagonists & inhibitors*
  • Receptor, Cannabinoid, CB1 / metabolism*
  • Tissue Distribution

Substances

  • Cannabinoid Receptor Antagonists
  • Pyrazoles
  • Pyridines
  • Receptor, Cannabinoid, CB1