The utilization of a unified pharmacophore query in the discovery of new antagonists of the adenosine receptor family

Bioorg Med Chem Lett. 2000 Jan 3;10(1):31-4. doi: 10.1016/s0960-894x(99)00583-1.

Abstract

Pharmacophore queries from previously known potent selective A3 antagonists were generated by Chem-X. These queries were used to search a pharmacophore database of diverse compounds (CNS-Set). In vitro assays of 186 'hits' yielded over 30 active compounds, for four adenosine receptor subtypes. This search strategy may also be applicable to the discovery of new ligands via receptor homology data.

MeSH terms

  • Adenosine-5'-(N-ethylcarboxamide) / pharmacology
  • Databases, Factual*
  • Flavonoids / chemistry
  • Flavonoids / pharmacology
  • Guanosine 5'-O-(3-Thiotriphosphate) / metabolism
  • Information Storage and Retrieval*
  • Kinetics
  • Ligands
  • Molecular Conformation
  • Purinergic P1 Receptor Antagonists*
  • Quinazolines / chemistry
  • Quinazolines / pharmacology
  • Receptor, Adenosine A3
  • Receptors, Purinergic P1 / classification
  • Receptors, Purinergic P1 / metabolism
  • Structure-Activity Relationship
  • Triazoles / chemistry
  • Triazoles / pharmacology

Substances

  • 3,6-dichloro-2'-isopropyloxy-4'-methylflavone
  • 9-chloro-2-(2-furyl)-5-phenylacetylamino(1,2,4)triazolo(1,5-c)quinazoline
  • Flavonoids
  • Ligands
  • Purinergic P1 Receptor Antagonists
  • Quinazolines
  • Receptor, Adenosine A3
  • Receptors, Purinergic P1
  • Triazoles
  • Adenosine-5'-(N-ethylcarboxamide)
  • Guanosine 5'-O-(3-Thiotriphosphate)