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dc.contributor.authorHuigens, Robert W., III
dc.contributor.authorRogers, Steven A.
dc.contributor.authorSteinhauer, Andrew T.
dc.contributor.authorMelander, Christian
dc.date.accessioned2015-11-20T23:05:36Z
dc.date.available2015-11-20T23:05:36Z
dc.date.issued2009-01-12
dc.identifier.citationIii, Robert W. Huigens, Steven A. Rogers, Andrew T. Steinhauer, and Christian Melander. "Inhibition of Acinetobacter Baumannii, Staphylococcus Aureus and Pseudomonas Aeruginosa Biofilm Formation with a Class of TAGE-triazole Conjugates." Organic & Biomolecular Chemistry Org. Biomol. Chem. 7.4 (2009): 794. DOI:10.1039/B817926Cen_US
dc.identifier.urihttp://hdl.handle.net/1808/18972
dc.descriptionThis is the published version. Copyright Royal Society of Chemistryen_US
dc.description.abstractA chemically diverse library of TAGE-triazole conjugates was synthesized utilizing click chemistry on the TAGE scaffold. This library of small molecules was screened for anti-biofilm activity and found to possess the ability of inhibiting biofilm formation against Acinetobacter baumannii, Staphylococcus aureus and Pseudomonas aeruginosa. One such compound in this library demonstrated the most potent inhibitory effect against Staphylococcus aureus biofilm formation that has been displayed by any 2-aminoimidazole derivative.en_US
dc.publisherRoyal Society of Chemistryen_US
dc.titleInhibition of Acinetobacter baumannii, Staphylococcus aureus and Pseudomonas aeruginosa biofilm formation with a class of TAGE-triazole conjugatesen_US
dc.typeArticle
kusw.kuauthorRogers, Steven A.
kusw.kudepartmentChemistryen_US
dc.identifier.doi10.1039/B817926C
kusw.oaversionScholarly/refereed, publisher version
kusw.oapolicyThis item meets KU Open Access policy criteria.
dc.rights.accessrightsopenAccess


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