Pyrazolo [4,3-c] quinolines synthesis and specific inhibition of benzodiazepine receptor binding. (Note I)

Abstract

A series of 2-arylpyrazolo[4,3-c] quinolin-3-one derivatives, bearing different substituents in the two aromatic rings, were prepared and tested for their ability to displace [3H] flunitrazepam from rat brain membranes. Some compounds have shown an affinity for receptors comparable and sometimes higher than that of CGS series.