Dual-action cephalosporins: cephalosporin 3'-quinolone carbamates

A series of cephalosporins has been prepared in which the 3'-position was linked to the nitrogen of the antibacterial quinolone ciprofloxacin through a carbamate function. Like the ester-linked and quaternary-linked dual-action cephalosporins reported earlier, these carbamate-linked compounds e...

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Veröffentlicht in:Journal of medicinal chemistry 1991-09, Vol.34 (9), p.2857-2864
Hauptverfasser: Albrecht, Harry A, Beskid, George, Georgopapadakou, Nafsika H, Keith, Dennis D, Konzelmann, Frederick M, Pruess, David L, Rossman, Pamela L, Wei, Chung Chen, Christenson, James G
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Sprache:eng
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Zusammenfassung:A series of cephalosporins has been prepared in which the 3'-position was linked to the nitrogen of the antibacterial quinolone ciprofloxacin through a carbamate function. Like the ester-linked and quaternary-linked dual-action cephalosporins reported earlier, these carbamate-linked compounds exhibited a broad antibacterial spectrum derived from both cephalosporin-like and quinolone-like activities, suggesting a dual mode of action. Studies to elucidate details of the mechanism of action have been inconclusive. Ciprofloxacin liberated as a consequence of bacterial enzyme-mediated reactions may contribute to the second mode of action, although some evidence indicates that the intact carbamate-linked bifunctional molecules may possess intrinsically both beta-lactam and quinolone activities.
ISSN:0022-2623
1520-4804
DOI:10.1021/jm00113a026