Tricyclic heteroaromatic systems. Pyrazolo[3,4-c]quinolin-4-ones and pyrazolo[3,4-c]quinoline-1,4-diones: synthesis and benzodiazepine receptor activity

Arch Pharm (Weinheim). 1997 Dec;330(12):383-6. doi: 10.1002/ardp.19973301205.

Abstract

Some pyrazolo[3,4-c]quinoline-4-ones 1-14 and pyrazolo[3,4-c]-quinoline-1,4-diones 15-17 were prepared and biologically evaluated for their binding at the benzodiazepine receptor (BZR) in rat cortical membranes. The moderate binding activity of 1-5, 7, 9-10, 13 is attributable to the lack of the optional proton acceptor at position-1, while the inactivity of the 1,4-dione derivatives 15-17 is due to the lack of the essential proton acceptor at position-3. These conclusions confirm the validity of our proposed pharmacophoric model.

MeSH terms

  • Animals
  • Male
  • Pyrazoles / chemical synthesis
  • Pyrazoles / metabolism*
  • Quinolines / chemical synthesis
  • Quinolines / metabolism*
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, GABA-A / metabolism*
  • Structure-Activity Relationship

Substances

  • Pyrazoles
  • Quinolines
  • Receptors, GABA-A