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Title: Synthesis and antibacterial activity of quinolone-based compounds containing a coumarin moiety. Author: Emami S, Foroumadi A, Faramarzi MA, Samadi N. Journal: Arch Pharm (Weinheim); 2008 Jan; 341(1):42-8. PubMed ID: 18072241. Abstract: A new series of quinolone-based compounds containing a coumarin moiety have been synthesized and studied for their antibacterial activity against a panel of gram-positive and gram-negative bacteria, including methicillin-resistant Staphylococcus aureus (MRSA). The results of the antibacterial evaluation of N-[2-(coumarin-3-yl)ethyl]piperazinyl quinolone derivatives in comparison with parent quinolones (norfloxacin, ciprofloxacin, and enoxacin) indicated that N-[2-(coumarin-3-yl)-2-oxoethyl]ciprofloxacin derivative (compound 8b) showed comparable or more potent antibacterial activity with respect to the reference drugs against the test strains. Generally, in both gram-positive and gram-negative bacteria, better results are obtained with cyclopropyl at the N-1 position of the quinolone ring and 2-oxo- on the ethyl spacer of coumarin and piperazine rings.[Abstract] [Full Text] [Related] [New Search]