In vitro antibacterial activity of AM-1155, a novel 6-fluoro-8-methoxy quinolone
Author(s) -
E. Wakabayashi,
S Mitsuhashi
Publication year - 1994
Publication title -
antimicrobial agents and chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.07
H-Index - 259
eISSN - 1070-6283
pISSN - 0066-4804
DOI - 10.1128/aac.38.3.594
Subject(s) - sparfloxacin , enterococcus faecalis , microbiology and biotechnology , staphylococcus aureus , antibacterial activity , pseudomonas aeruginosa , streptococcus pneumoniae , quinolone , minimum inhibitory concentration , broth microdilution , antibacterial agent , enterococcus , escherichia coli , enterobacteriaceae , bacteria , biology , chemistry , antibiotics , ofloxacin , ciprofloxacin , biochemistry , genetics , gene
The in vitro antibacterial activity of AM-1155 against a wide variety of clinical isolates was compared with those of other fluoroquinolones. The MICs of AM-1155 for 90% of Staphylococcus aureus, Streptococcus pneumoniae, and Enterococcus faecalis isolates tested were 0.10, 0.39, and 0.78 microgram/ml, respectively. The antibacterial activity of AM-1155 against gram-positive bacteria and anaerobes was comparable to those of sparfloxacin and tosufloxacin. AM-1155 inhibited 90% of most species of the family Enterobacteriaceae at a concentration of 0.39 microgram/ml. AM-1155 generally had activity comparable to that of sparfloxacin against gram-negative bacteria. AM-1155 showed moderate activity against methicillin- and quinolone-resistant S. aureus. AM-1155 demonstrated bactericidal activity at the MIC. The frequency of occurrence of spontaneous mutants resistant to four times the MIC of AM-1155 was < 1 x 10(9) for S. aureus, Escherichia coli, and Pseudomonas aeruginosa. AM-1155 strongly inhibited the supercoiling activities of DNA gyrases purified from E. coli and S. aureus.
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