| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1256236 | Chinese Chemical Letters | 2007 | 4 Pages |
Abstract
Several 6,8-dichloroquinolone analogues were synthesized from the key intermediate compound of 2,3,4,5-tetrachlorobenzene carbonyl chloride, which was obtained from the starting material of tetrachlorophthalic anhydride. Their in vitro antibacterial activities were evaluated. As a result of this study, compounds 21c and 21d were twofold more potent than ciprofloxacin (CPFX) and norfloxacin (NFLX) against Staphylococcus aureus-9, and with the same potent as CPFX and NFLX while against Escherichia coli-2, but were less potent than references in against Pseudomonas aeruginosa-17.
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Physical Sciences and Engineering
Chemistry
Chemistry (General)
Authors
Yun Xu Yang, Hui Yuan Guo,