Novel 3,6,7-substituted pyrazolopyrimidines as positive allosteric modulators for the hydroxycarboxylic acid receptor 2 (GPR109A)

J Med Chem. 2012 Apr 12;55(7):3563-7. doi: 10.1021/jm300164q. Epub 2012 Mar 27.

Abstract

A number of pyrazolopyrimidines were synthesized and tested for their positive allosteric modulation of the HCA(2) receptor (GPR109A). Compound 24, an efficacious and potent agonist and allosteric enhancer of nicotinic acid's action, was the basis for most other compounds. Interestingly, some of the compounds were found to increase the efficacy of the endogenous ligand 3-hydroxybutyrate and enhance its potency almost 10-fold. This suggests that the pyrazolopyrimidines may have therapeutic value when given alone.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3-Hydroxybutyric Acid / metabolism
  • Allosteric Regulation
  • Drug Synergism
  • Guanosine 5'-O-(3-Thiotriphosphate) / pharmacology
  • HEK293 Cells
  • Humans
  • Niacin / pharmacology
  • Pyrazoles / chemical synthesis*
  • Pyrazoles / chemistry
  • Pyrazoles / pharmacology
  • Pyrimidines / chemical synthesis*
  • Pyrimidines / chemistry
  • Pyrimidines / pharmacology
  • Radioligand Assay
  • Receptors, G-Protein-Coupled / agonists
  • Receptors, G-Protein-Coupled / metabolism*
  • Receptors, Nicotinic / metabolism*
  • Structure-Activity Relationship

Substances

  • HCAR2 protein, human
  • Pyrazoles
  • Pyrimidines
  • Receptors, G-Protein-Coupled
  • Receptors, Nicotinic
  • Niacin
  • Guanosine 5'-O-(3-Thiotriphosphate)
  • 3-Hydroxybutyric Acid