期刊
JOURNAL OF HETEROCYCLIC CHEMISTRY
卷 55, 期 10, 页码 2434-2440出版社
WILEY
DOI: 10.1002/jhet.3279
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A series of 8-methoxyl ciprofloxacin (8-OMe CPFX)-isatin hybrids 3a-f and 4a-f tethered through propylene were designed, synthesized, and examined for their in vitro antibacterial activities against a panel of Gram-positive and Gram-negative pathogens including drug-resistant bacteria. All the synthesized hybrids (minimum inhibitory concentration: 0.03-64g/mL) exhibited considerable activities against the tested strains, especially against the Gram-negative pathogens. Among them, hybrid 3b was no inferior to the parent 8-OMe CPFX that could act as a starting point for further optimization.
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