In vitro activity of six quinolone derivatives against Neisseria gonorrhoeae.

@article{Lefevre1988InVA,
  title={In vitro activity of six quinolone derivatives against Neisseria gonorrhoeae.},
  author={Jonathan Lefevre and M C Tempesta and E Gaubert and M B Lareng},
  journal={Chemotherapy},
  year={1988},
  volume={34 4},
  pages={315-7}
}
The in vitro activities of six quinolone derivatives, rosoxacin, pefloxacin, ofloxacin, ciprofloxacin, A-56619 and A-56620, were compared with those of penicillin, cefotaxime, spectinomycin, chloramphenicol, tetracycline and erythromycin against 50 nonpenicillinase-producing and 15 penicillinase-producing Neisseria gonorrhoeae strains. Ciprofloxacin was the most active compound in vitro (MIC50, 0.004 mg/l) followed by ofloxacin and A-56620 (MIC50, 0.008 mg/l), A-56619 and cefotaxime (MIC50, 0… CONTINUE READING

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