| Literature DB >> 1910090 |
H A Albrecht1, G Beskid, J G Christenson, N H Georgopapadakou, D D Keith, F M Konzelmann, D L Pruess, P L Rossman, C C Wei.
Abstract
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.Entities:
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Year: 1991 PMID: 1910090 DOI: 10.1021/jm00113a026
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446