Pyrimido[1,6-a]benzimidazoles: a new class of DNA gyrase inhibitors

J Med Chem. 1992 Apr 17;35(8):1385-92. doi: 10.1021/jm00086a006.

Abstract

Substituted 4-quinolone- (1, A = CH) and 1,8-naphthyrid-4-one- (1, A = N) 3-carboxylic acids are currently the only classes of clinically useful antibacterial agents exerting their activity by inhibiting the subunit A of DNA gyrase. Pyrimido[1,6-alpha]benzimidazoles 11 have been found to be a new class of inhibitors of this enzyme. The design, synthesis, and biological activity of these compounds are reported.

MeSH terms

  • Benzimidazoles / chemical synthesis*
  • Benzimidazoles / chemistry
  • Benzimidazoles / pharmacology
  • Enzyme Inhibitors / chemical synthesis
  • Pyrimidinones / chemical synthesis*
  • Pyrimidinones / chemistry
  • Pyrimidinones / pharmacology
  • Structure-Activity Relationship
  • Topoisomerase II Inhibitors*

Substances

  • Benzimidazoles
  • Enzyme Inhibitors
  • Pyrimidinones
  • Topoisomerase II Inhibitors