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Synthesis and antimicrobial activity of binaphthyl-based, functionalized oxazole and thiazole peptidomimetics

journal contribution
posted on 2024-11-16, 06:56 authored by Steven Wales, Katherine A Hammer, Kittiya Somphol, Isabell Kemker, David C Schröder, Andrew TagueAndrew Tague, Zinka Brkic, Amy M King, Dena Lyras, Thomas V Riley, John BremnerJohn Bremner, Paul KellerPaul Keller, Stephen PyneStephen Pyne
Thirty two new binaphthyl-based, functionalized oxazole and thiazole peptidomimetics and over thirty five novel leucine-containing intermediate oxazoles and thiazoles were prepared in this study. This includes the first examples of the direct C-5 arylation of an amino acid dipeptide-derived oxazole. Moderate to excellent antibacterial activity was observed for all new compounds across Gram positive isolates with MICs ranging from 1-16 μg mL−1. Results for Gram negative E. coli and A. baumannii were more variable, but MICs as low as 4 μg mL−1 were returned for two examples. Significantly, the in vitro results with a fluoromethyl-oxazole derivative collectively represent the best obtained to date for a member of our binaphthyl peptide antimicrobials.

Funding

The Development Of Novel Antibacterials Targeting Clostridium Difficile Infections

National Health and Medical Research Council

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History

Citation

Wales, S. M., Hammer, K. A., Somphol, K., Kemker, I., Schröder, D. C., Tague, A. J., Brkic, Z., King, A. M., Lyras, D., Riley, T. V., Bremner, J. B., Keller, P. A. & Pyne, S. G. (2015). Synthesis and antimicrobial activity of binaphthyl-based, functionalized oxazole and thiazole peptidomimetics. Organic and Biomolecular Chemistry, 13 (44), 10813-10824.

Journal title

Organic and Biomolecular Chemistry

Volume

13

Issue

44

Pagination

10813-10824

Language

English

RIS ID

103998

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