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Facile Solid-Phase Synthesis of Well-Defined Defect Lysine Dendrimers

[Image: see text] An efficient solid-phase method has been reported to prepare well-defined lysine defect dendrimers. Using orthogonally protected lysine residues, pure G2 to G4 lysine defect dendrimers were prepared with 48–95% yields within 13 h. Remarkably, high-purity products were collected via...

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Autores principales: Liao, Yong, Chan, Yuan-Ting, Molakaseema, Vijayasimha, Selvaraj, Anand, Chen, Hui-Ting, Wang, Yun-Ming, Choo, Yeun-Mun, Kao, Chai-Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9260950/
https://www.ncbi.nlm.nih.gov/pubmed/35811872
http://dx.doi.org/10.1021/acsomega.2c02708
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author Liao, Yong
Chan, Yuan-Ting
Molakaseema, Vijayasimha
Selvaraj, Anand
Chen, Hui-Ting
Wang, Yun-Ming
Choo, Yeun-Mun
Kao, Chai-Lin
author_facet Liao, Yong
Chan, Yuan-Ting
Molakaseema, Vijayasimha
Selvaraj, Anand
Chen, Hui-Ting
Wang, Yun-Ming
Choo, Yeun-Mun
Kao, Chai-Lin
author_sort Liao, Yong
collection PubMed
description [Image: see text] An efficient solid-phase method has been reported to prepare well-defined lysine defect dendrimers. Using orthogonally protected lysine residues, pure G2 to G4 lysine defect dendrimers were prepared with 48–95% yields within 13 h. Remarkably, high-purity products were collected via precipitation without further purification steps. This method was applied to prepare a pair of 4-carboxyphenylboronic acid-decorated defect dendrimers (16 and 17), which possessed the same number of boronic acids. The binding affinity of 16, in which the ε-amines of G1 lysine are fractured, for glucose and sorbitol was 4 times that of 17. This investigation indicated the role of allocation and distribution of peripheries for the dendrimer’s properties and activity.
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spelling pubmed-92609502022-07-08 Facile Solid-Phase Synthesis of Well-Defined Defect Lysine Dendrimers Liao, Yong Chan, Yuan-Ting Molakaseema, Vijayasimha Selvaraj, Anand Chen, Hui-Ting Wang, Yun-Ming Choo, Yeun-Mun Kao, Chai-Lin ACS Omega [Image: see text] An efficient solid-phase method has been reported to prepare well-defined lysine defect dendrimers. Using orthogonally protected lysine residues, pure G2 to G4 lysine defect dendrimers were prepared with 48–95% yields within 13 h. Remarkably, high-purity products were collected via precipitation without further purification steps. This method was applied to prepare a pair of 4-carboxyphenylboronic acid-decorated defect dendrimers (16 and 17), which possessed the same number of boronic acids. The binding affinity of 16, in which the ε-amines of G1 lysine are fractured, for glucose and sorbitol was 4 times that of 17. This investigation indicated the role of allocation and distribution of peripheries for the dendrimer’s properties and activity. American Chemical Society 2022-06-17 /pmc/articles/PMC9260950/ /pubmed/35811872 http://dx.doi.org/10.1021/acsomega.2c02708 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Liao, Yong
Chan, Yuan-Ting
Molakaseema, Vijayasimha
Selvaraj, Anand
Chen, Hui-Ting
Wang, Yun-Ming
Choo, Yeun-Mun
Kao, Chai-Lin
Facile Solid-Phase Synthesis of Well-Defined Defect Lysine Dendrimers
title Facile Solid-Phase Synthesis of Well-Defined Defect Lysine Dendrimers
title_full Facile Solid-Phase Synthesis of Well-Defined Defect Lysine Dendrimers
title_fullStr Facile Solid-Phase Synthesis of Well-Defined Defect Lysine Dendrimers
title_full_unstemmed Facile Solid-Phase Synthesis of Well-Defined Defect Lysine Dendrimers
title_short Facile Solid-Phase Synthesis of Well-Defined Defect Lysine Dendrimers
title_sort facile solid-phase synthesis of well-defined defect lysine dendrimers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9260950/
https://www.ncbi.nlm.nih.gov/pubmed/35811872
http://dx.doi.org/10.1021/acsomega.2c02708
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