Tricyclic heteroaromatic systems. Synthesis and benzodiazepine binding activity of 1-substituted-3-methyl- and 3-phenylpyrazolo[4,5-c]quinolin-4-ones

Drug Des Discov. 1992 Jul;8(4):325-39.

Abstract

The synthesis and the benzodiazepine binding activity of some 3-methyl- and 3-phenylpyrazolo[4,5-c]quinolin-4-ones bearing a heterocyclic or a substituent which is different from an aryl moiety at position-1 are reported. Molecular modelling is used to correlate the binding affinity to the chemical features and to justify the reduced receptor affinities of the reported compounds with respect to that of CGS 8216 which is taken as the lead compound.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cattle
  • In Vitro Techniques
  • Mice
  • Models, Molecular
  • Quinolones / chemical synthesis*
  • Quinolones / chemistry
  • Quinolones / metabolism
  • Receptors, GABA-A / metabolism*
  • Structure-Activity Relationship

Substances

  • Quinolones
  • Receptors, GABA-A