3-Phenyl-5-isothiazole carboxamides with potent mGluR1 antagonist activity

Bioorg Med Chem Lett. 2012 Apr 1;22(7):2514-7. doi: 10.1016/j.bmcl.2012.02.003. Epub 2012 Feb 9.

Abstract

The disclosed 3-phenyl-5-isothiazole carboxamides are potent allosteric antagonists of mGluR1 with generally good selectivity relative to the related group 1 receptor mGluR5. Pharmacokinetic properties of a member of this series (1R,2R)-N-(3-(4-methoxyphenyl)-4-methylisothiazol-5-yl)-2-methylcyclopropanecarboxamide (14) are good, showing acceptable plasma and brain exposure after oral dosing. Oral administration of isothiazole 14 gave robust activity in the formalin model of persistent pain which correlated with CNS receptor occupancy.

MeSH terms

  • Administration, Oral
  • Amides / administration & dosage
  • Amides / chemical synthesis*
  • Amides / pharmacokinetics
  • Analgesics / administration & dosage
  • Analgesics / chemical synthesis*
  • Analgesics / pharmacokinetics
  • Animals
  • Biological Availability
  • Brain / metabolism
  • Excitatory Amino Acid Antagonists / administration & dosage
  • Excitatory Amino Acid Antagonists / chemical synthesis*
  • Excitatory Amino Acid Antagonists / pharmacokinetics
  • Humans
  • Pain / drug therapy*
  • Pain / metabolism
  • Pain Measurement
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Metabotropic Glutamate / antagonists & inhibitors*
  • Receptors, Metabotropic Glutamate / metabolism
  • Stereoisomerism
  • Structure-Activity Relationship
  • Thiazoles / administration & dosage
  • Thiazoles / chemical synthesis*
  • Thiazoles / pharmacokinetics

Substances

  • Amides
  • Analgesics
  • Excitatory Amino Acid Antagonists
  • Receptors, Metabotropic Glutamate
  • Thiazoles
  • metabotropic glutamate receptor type 1