Comparison of the antibacterial activities of the quinolones Bay 12-8039, gatifloxacin (AM 1155), trovafloxacin, clinafloxacin, levofloxacin and ciprofloxacin

J Antimicrob Chemother. 1997 Nov;40(5):639-51. doi: 10.1093/jac/40.5.639.

Abstract

The in-vitro activities of the quinolones Bay 12-8039, gatifloxacin (AM 1155), trovafloxacin, clinafloxacin, levofloxacin and ciprofloxacin were compared. Gram-positive cocci were most susceptible to Bay 12-8039, clinafloxacin and trovafloxacin; Enterobacteriaceae and fastidious organisms were most susceptible to clinafloxacin [corrected]; Pseudomonas spp. were most susceptible to clinafloxacin and ciprofloxacin; anaerobes, Helicobacter pylori and Campylobacter jejuni were most susceptible to gatifloxacin, clinafloxacin and trovafloxacin. Against gram-positive cocci, the only agents that were more active than ciprofloxacin were those carrying an azabicyclo (trovafloxacin, Bay 12-8039), 3-amino-pyrrolidinyl (clinafloxacin) or 3-methyl-piperazinyl (gatifloxacin) moiety at position C7.

Publication types

  • Comparative Study

MeSH terms

  • Anti-Infective Agents / pharmacology*
  • Aza Compounds*
  • Bacteria / drug effects*
  • Ciprofloxacin / pharmacology
  • Enterobacteriaceae / drug effects
  • Fluoroquinolones*
  • Gatifloxacin
  • Levofloxacin
  • Microbial Sensitivity Tests
  • Moxifloxacin
  • Naphthyridines / pharmacology
  • Ofloxacin / pharmacology
  • Piperazines / pharmacology
  • Quinolines*
  • Quinolones / pharmacology
  • Staphylococcus aureus / drug effects

Substances

  • Anti-Infective Agents
  • Aza Compounds
  • Fluoroquinolones
  • Naphthyridines
  • Piperazines
  • Quinolines
  • Quinolones
  • Ciprofloxacin
  • Levofloxacin
  • clinafloxacin
  • trovafloxacin
  • Ofloxacin
  • Gatifloxacin
  • Moxifloxacin