| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 1373072 | Bioorganic & Medicinal Chemistry Letters | 2008 | 4 Pages | 
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.
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													Physical Sciences and Engineering
													Chemistry
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											Authors
												T. Kline, M.S. Trent, C.M. Stead, M.S. Lee, M.C. Sousa, H.B. Felise, H.V. Nguyen, S.I. Miller, 
											