Pyridazine N-oxides. III. Synthesis and "in vitro" antimicrobial properties of N-oxide derivatives based on tricyclic indeno[2,1-c]pyridazine and benzo[f]cinnoline systems

Arch Pharm (Weinheim). 2000 Oct;333(10):341-6. doi: 10.1002/1521-4184(200010)333:10<341::aid-ardp341>3.0.co;2-u.

Abstract

A number of 9H-indeno[2,1-c]pyridazine N-oxides (3a-c) and benzo[f]cinnoline N-oxides (4,5a-c) have been synthesized and tested for antimicrobial activity. All new products were inactive against Gram negative bacteria and fungi. In contrast, among the compounds synthesized, 3b, 4b and 5b showed a moderate activity against Gram positive Staphylococcus aureus and Staphylococcus epidermidis. Of the present series, the 9-nitro-benzo[f]cinnoline N-oxide 5b possessed the highest activity especially against Trichomonas vaginalis (MIC = 3.9 micrograms/ml).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents / chemical synthesis*
  • Phenanthrenes / chemical synthesis*
  • Phenanthrenes / pharmacology
  • Pyridazines / chemical synthesis*
  • Pyridazines / pharmacology

Substances

  • Anti-Bacterial Agents
  • Phenanthrenes
  • Pyridazines
  • benzo(c)cinnoline