Publication | Open Access
In vitro activity of DR-3355, an optically active ofloxacin
144
Citations
12
References
1988
Year
Human UrinePharmaceutical ScienceAntimicrobial SusceptibilityActive OfloxacinAntibioticsHealth SciencesMedicineAntibiotic AdjuvantDifferent MediaSelective ToxicityAntimicrobial ChemotherapyMicrobiologyHuman SerumPharmacologyClinical MicrobiologyAntimicrobial ResistanceDrug DiscoveryDrug Resistance
DR-3355, the S-(-)-isomer of ofloxacin, was generally twice as potent as ofloxacin against a variety of gram-positive and gram-negative pathogens, and its action was bactericidal. The compound was characterized by having the highest level of activity against staphylococci, Bacteroides fragilis, and Peptococcus spp. of the fluorinated quinolones tested, including ofloxacin, ciprofloxacin, fleroxacin, and NY-198. The activity of DR-3355 was not affected by different media, inoculum size, or human serum, but decreased under acidic conditions at pH 5.0 or in human urine.
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