期刊
CHEMISTRY & BIODIVERSITY
卷 15, 期 10, 页码 -出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/cbdv.201800273
关键词
ciprofloxacin; dithiocarbamate; docking study; antibacterial activity; BIODS
资金
- research council of TUMS (Tehran University of Medical Sciences)
A novel series of ciprofloxacin-dithiocarbamate hybrids 7a-7l were designed, synthesized, and evaluated against Gram-positive and Gram-negative bacteria. A significant part of the title compounds showed considerable antibacterial activity against Gram-positive species. The most potent compound against Gram-positive bacteria was 2-chloro derivative 7h and the most potent derivative against Gram-negative bacteria was 3-chloro compound 7i. Invitro antibacterial evaluation of compound 7h against clinically isolated bacteria methicillin-resistant Staphylococcus aureus (MRSA) and methicillin-sensitive Staphylococcus aureus (MSSA) showed that this compound acted better than ciprofloxacin against the latter bacteria. Docking study of compound 7h in the active site of S.aureus DNA gyrase revealed that this ciprofloxacin-dithiocarbamate derivative interacted with the main components of the active site of the enzyme.
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