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Updated: May 18, 2026

An Efficient Method for the Synthesis of Peptoids with Mixed Lysine-type/Arginine-type Monomers and Evaluation of Their Anti-leishmanial Activity
Published on: November 2, 2016
Binaphthyl-anchored antibacterial tripeptide derivatives with hydrophobic C-terminal amino acid variations
John B Bremner1, Paul A Keller, Stephen G Pyne
1School of Chemistry, University of Wollongong, Wollongong, NSW 2522, Australia.
Abstract:
The facile synthesis of seven new dicationic tripeptide benzyl ester derivatives, with hydrophobic group variations in the C-terminal amino acid component, is described. Moderate to good activity was seen against Gram-positive bacteria in vitro. One cyclohexyl-substituted compound 2c was tested more widely and showed good potency (MIC values ranging from 2-4 μg/mL) against antibiotic-resistant strains of Staphylococcus aureus and Enterococci (VRE, VSE), and against Staphylococcus epidermidis.
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