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Binaphthyl-anchored antibacterial tripeptide derivatives with hydrophobic C-terminal amino acid variations

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posted on 2024-11-14, 14:33 authored by John BremnerJohn Bremner, Paul KellerPaul Keller, Stephen PyneStephen Pyne, Mark Robertson, Kandasamy Sakthivel, Kittiya Somphol, Dean Baylis, Jonathon A Coates, John Deadman, Dharshini Jeevarajah, David Rhodes
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.

History

Citation

Bremner, J., Keller, P., Pyne, S., Robertson, M., Sakthivel, K., Somphol, K., Baylis, D., Coates, J., Deadman, J., Jeevarajah, D., Rhodes, D. (2012). Binaphthyl-anchored antibacterial tripeptide derivatives with hydrophobic C-terminal amino acid variations. Beilstein Journal of Organic Chemistry, 8 1265-1270.

Journal title

Beilstein Journal of Organic Chemistry

Volume

8

Pagination

1265-1270

Language

English

RIS ID

63630

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