9H-Xanthene-9-carboxylic acid [1,2,4]oxadiazol-3-yl- and (2H-tetrazol-5-yl)-amides as potent, orally available mGlu1 receptor enhancers

Bioorg Med Chem Lett. 2005 Oct 15;15(20):4628-31. doi: 10.1016/j.bmcl.2005.05.135.

Abstract

Small molecule mGluR1 enhancers based on the lead compound (9H-xanthene-9-carbonyl)-carbamic acid butyl ester derived from random-screening hit diphenylacetyl-carbamic acid ethyl ester were designed and synthesized as useful pharmacological tools for the study of the physiological roles mediated by mGlu1 receptors. The synthesis and the structure-activity relationship of this new class of positive allosteric modulators of mGlu1 receptors will be discussed in detail.

MeSH terms

  • Allosteric Regulation
  • Animals
  • Excitatory Amino Acid Agonists / administration & dosage
  • Excitatory Amino Acid Agonists / chemistry
  • Excitatory Amino Acid Agonists / pharmacokinetics
  • Excitatory Amino Acid Agonists / pharmacology*
  • Oxadiazoles / administration & dosage
  • Oxadiazoles / chemistry
  • Oxadiazoles / pharmacokinetics
  • Oxadiazoles / pharmacology*
  • Rats
  • Receptors, Metabotropic Glutamate / agonists*
  • Spectrometry, Fluorescence
  • Tetrazoles / administration & dosage
  • Tetrazoles / chemistry
  • Tetrazoles / pharmacokinetics
  • Tetrazoles / pharmacology*

Substances

  • Excitatory Amino Acid Agonists
  • Oxadiazoles
  • Receptors, Metabotropic Glutamate
  • Tetrazoles
  • metabotropic glutamate receptor type 1