| Literature DB >> 18187325 |
T Kline1, M S Trent, C M Stead, M S Lee, M C Sousa, H B Felise, H V Nguyen, S I Miller.
Abstract
Three sets of novel 4-deoxy-l-arabinose analogs were synthesized and evaluated as potential inhibitors of the bacterial resistance mechanism in which lipid A, on the outer membrane, is modified with 4-amino-4-deoxy-l-arabinose (l-Ara4N). One compound diminished the transfer of l-Ara4N onto lipid A. These results suggest that small molecules might be designed that would effect the same reversal of bacterial resistance observed in genetic knockouts.Entities:
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Year: 2007 PMID: 18187325 PMCID: PMC2516481 DOI: 10.1016/j.bmcl.2007.12.061
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823