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Syntheses of Sulfo-Glycodendrimers Using Click Chemistry and Their Biological Evaluation
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-termina...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268394/ https://www.ncbi.nlm.nih.gov/pubmed/23047486 http://dx.doi.org/10.3390/molecules171011877 |
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author | Miura, Yoshiko Onogi, Shunsuke Fukuda, Tomohiro |
author_facet | Miura, Yoshiko Onogi, Shunsuke Fukuda, Tomohiro |
author_sort | Miura, Yoshiko |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6268394 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62683942018-12-12 Syntheses of Sulfo-Glycodendrimers Using Click Chemistry and Their Biological Evaluation Miura, Yoshiko Onogi, Shunsuke Fukuda, Tomohiro Molecules Article 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. MDPI 2012-10-09 /pmc/articles/PMC6268394/ /pubmed/23047486 http://dx.doi.org/10.3390/molecules171011877 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Miura, Yoshiko Onogi, Shunsuke Fukuda, Tomohiro Syntheses of Sulfo-Glycodendrimers Using Click Chemistry and Their Biological Evaluation |
title | Syntheses of Sulfo-Glycodendrimers Using Click Chemistry and Their Biological Evaluation |
title_full | Syntheses of Sulfo-Glycodendrimers Using Click Chemistry and Their Biological Evaluation |
title_fullStr | Syntheses of Sulfo-Glycodendrimers Using Click Chemistry and Their Biological Evaluation |
title_full_unstemmed | Syntheses of Sulfo-Glycodendrimers Using Click Chemistry and Their Biological Evaluation |
title_short | Syntheses of Sulfo-Glycodendrimers Using Click Chemistry and Their Biological Evaluation |
title_sort | syntheses of sulfo-glycodendrimers using click chemistry and their biological evaluation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268394/ https://www.ncbi.nlm.nih.gov/pubmed/23047486 http://dx.doi.org/10.3390/molecules171011877 |
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