Syntheses of sulfo-glycodendrimers using click chemistry and their biological evaluation

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Abstract

A series of novel glycol-clusters containing sulfonated N-acetyl-D-glucosamine (GlcNAc) have been synthesized using click chemistry. Three dendrimers with aromatic dendrons were synthesized using chlorination, azidation and click chemistries. The resulting dendrimers were modified with azide-terminated sulfonated GlcNAc using click chemistry. The sulfonated dendrimers showed affinity for proteins, including the lectin wheat germ agglutinin and amyloid beta peptide (1-42). The dendrimers of G1 and G2 in particular showed the largest affinity for the proteins. The addition of the sulfonated GlcNAc dendrimers of G1 and G2 exhibited an inhibition effect on the aggregation of the amyloid beta peptide, reduced the β-sheet conformation, and led to a reduction in the level of nanofiber formation. © 2012 by the authors; licensee MDPI, Basel, Switzerland.

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Miura, Y., Onogi, S., & Fukuda, T. (2012). Syntheses of sulfo-glycodendrimers using click chemistry and their biological evaluation. Molecules, 17(10), 11877–11896. https://doi.org/10.3390/molecules171011877

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