NEW 8-(TRIFLUOROMETHYL)-SUBSTITUTED QUINOLONES - THE BENEFITS OF THE 8-FLUORO GROUP WITH REDUCED PHOTOTOXIC RISK

被引:31
作者
SANCHEZ, JP
BRIDGES, AJ
BUCSH, R
DOMAGALA, JM
GOGLIOTTI, RD
HAGEN, SE
HEIFETZ, CL
JOANNIDES, ET
SESNIE, JC
SHAPIRO, MA
SZOTEK, DL
机构
[1] Parke-Davis Pharmaceutical Research Division, Warner-Lambert Company, Ann Arbor
关键词
D O I
10.1021/jm00080a023
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of 8-(trifluoromethyl)-substituted quinolones has been prepared and evaluated for in vitro and in vivo antibacterial activity, and phototolerance in a mouse phototolerance assay. These analogues were compared to the corresponding series of 6,8-difluoro- and 6-fluoro-8H-quinolones (ciprofloxacin type). Although their in vitro antibacterial activities are less than the 6,8-difluoro analogues, the 8-(trifluoromethyl)quinolones are generally equivalent to their 8H analogues. In vivo, they are comparable to the 6,8-difluoro series and show up to 10-fold improvement in efficacy when compared to their ciprofloxacin counterparts vs Streptococcus pyogenes and Streptococcus pneumonia. In the phototolerance model, the 8-(trifluoromethyl)quinolones are comparable to the 8H-quinolones. Both of these series display much higher no effect doses (greater tolerance) than the corresponding 6,8-difluoroquinolones.
引用
收藏
页码:361 / 367
页数:7
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