Issue 4, 2009

Inhibition of Acinetobacter baumannii, Staphylococcus aureus and Pseudomonas aeruginosabiofilm formation with a class of TAGE-triazole conjugates

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.

Graphical abstract: Inhibition of Acinetobacter baumannii, Staphylococcus aureus and Pseudomonas aeruginosa biofilm formation with a class of TAGE-triazole conjugates

Supplementary files

Article information

Article type
Paper
Submitted
13 Oct 2008
Accepted
20 Nov 2008
First published
12 Jan 2009

Org. Biomol. Chem., 2009,7, 794-802

Inhibition of Acinetobacter baumannii, Staphylococcus aureus and Pseudomonas aeruginosa biofilm formation with a class of TAGE-triazole conjugates

R. W. Huigens III, S. A. Rogers, A. T. Steinhauer and C. Melander, Org. Biomol. Chem., 2009, 7, 794 DOI: 10.1039/B817926C

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