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Inhibition of Acinetobacter baumannii, Staphylococcus aureus and Pseudomonas aeruginosa biofilm formation with a class of TAGE-triazole conjugates
Huigens, Robert W., III Rogers, Steven A. Steinhauer, Andrew T. Melander, Christian
Huigens, Robert W., III
Rogers, Steven A.
Steinhauer, Andrew T.
Melander, Christian
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Abstract
A 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.
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This is the published version. Copyright Royal Society of Chemistry
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2009-01-12
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Royal Society of Chemistry
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Iii, 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/B817926C