Inhibition of Acinetobacter baumannii, Staphylococcus aureus and Pseudomonas aeruginosa biofilm formation with a class of TAGE-triazole conjugates
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Issue Date
2009-01-12Author
Huigens, Robert W., III
Rogers, Steven A.
Steinhauer, Andrew T.
Melander, Christian
Publisher
Royal Society of Chemistry
Type
Article
Article Version
Scholarly/refereed, publisher version
Metadata
Show full item recordAbstract
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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Citation
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
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