Expeditive synthesis of trithiotriazine-cored glycoclusters and inhibition of Pseudomonas aeruginosa biofilm formation

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Abstract

Readily accessible, low-valency glycoclusters based on a triazine core bearing D-galactose and L-fucose epitopes are able to inhibit biofilm formation by Pseudomonas aeruginosa. These multivalent ligands are simple to synthesize, are highly soluble, and can be either homofunctional or heterofunctional. The galactose-decorated cluster shows good affinity for Pseudomonas aeruginosa lectin lecA. They are convenient biological probes for investigating the roles of lecA and lecB in biofilm formation. © 2014 Smadhi et al; licensee Beilstein-Institut.

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Smadhi, M., De Bentzmann, S., Imberty, A., Gingras, M., Abderrahim, R., & Goekjian, P. G. (2014). Expeditive synthesis of trithiotriazine-cored glycoclusters and inhibition of Pseudomonas aeruginosa biofilm formation. Beilstein Journal of Organic Chemistry, 10, 1981–1990. https://doi.org/10.3762/bjoc.10.206

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