Publication | Open Access
Inhibition of Acinetobacter baumannii, Staphylococcus aureus and Pseudomonas aeruginosa biofilm formation with a class of TAGE-triazole conjugates
58
Citations
20
References
2009
Year
Bioorganic ChemistryStaphylococcus AureusAntimicrobial ChemotherapyClick ChemistryPharmaceutical ChemistryDrug ResistanceMedicinal ChemistryBiofilm FormationInfection ControlAntimicrobial ResistanceHealth SciencesTage-triazole ConjugatesTage ScaffoldAntibacterial AgentAntimicrobial CompoundPharmacologyClinical MicrobiologyAntimicrobial SusceptibilityAntibioticsMicrobiologyMedicineDrug Discovery
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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