| Literature DB >> 19719234 |
Justin J Richards1, Samuel Reyes, Sean D Stowe, Ashley T Tucker, T Eric Ballard, Laura D Mathies, John Cavanagh, Christian Melander.
Abstract
The synthesis and antibiofilm activities of sulfonamide, urea, and thiourea oroidin analogues are described. The most active derivative was able to selectively inhibit P. aeruginosa biofilm development and is also shown to be nontoxic upward of 1 mM to the development of C. elegans in comparison to other similar isosteric analogues and the natural product oroidin.Entities:
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Year: 2009 PMID: 19719234 PMCID: PMC2739084 DOI: 10.1021/jm900378s
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446