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作为重复的d-GlcN-α-1,4-d-GlcA硫酸乙酰肝素二糖模拟物的β-糖苷构建块的合成。

Synthesis of -Glycoside Building Blocks as Mimetics of the Repeating d-GlcN-α-1,4-d-GlcA Heparan Sulfate Disaccharide.

作者信息

O'Shea Conor, Miller Gavin J

机构信息

School of Chemical and Physical Sciences and Centre for Glycoscience, Keele University, Keele, Staffordshire ST5 5BG, UK.

出版信息

Molecules. 2024 Dec 9;29(23):5809. doi: 10.3390/molecules29235809.

Abstract

Heparan sulfate (HS), a sulfated linear carbohydrate that decorates the cell surface and extracellular matrix, is a key regulator of biological processes. Owing to the inherent structural complexity of HS, structure-to-function studies with its ligands are required, and materials to improve the understanding of such interactions are therefore of high importance. Herein, the synthesis of novel -linked GlcN-α(1→4)-GlcA disaccharide building blocks is detailed. Initial attempts at constructing the desired disaccharide using d-GlcN donors and d-Glc/GlcA acceptors via an -glycosylation failed. Reversing the reactivity polarity of the monosaccharide building blocks enabled successful S2 coupling using α-d-GlcN thiohemiacetals and d-galactosyl triflates. Subsequent C6-oxidation furnished the desired -linked GlcN-α(1→4)-GlcA disaccharide building blocks on a gram scale. Such disaccharides offer potential for incorporation into wider synthetic HS sequences to provide glycomimetic tools.

摘要

硫酸乙酰肝素(HS)是一种修饰细胞表面和细胞外基质的硫酸化线性碳水化合物,是生物过程的关键调节因子。由于HS固有的结构复杂性,需要对其与配体进行结构与功能研究,因此有助于增进对此类相互作用理解的材料具有高度重要性。本文详细介绍了新型β-连接的GlcN-α(1→4)-GlcA二糖结构单元的合成。最初尝试通过β-糖基化反应,使用d-GlcN供体和d-Glc/GlcA受体构建所需二糖,但未成功。通过反转单糖结构单元的反应活性极性,使用α-d-GlcN硫代半缩醛和d-半乳糖基三氟甲磺酸酯实现了成功的S2偶联。随后的C6氧化反应以克级规模提供了所需的β-连接的GlcN-α(1→4)-GlcA二糖结构单元。此类二糖具有被纳入更广泛的合成HS序列以提供糖模拟工具的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/283f/11643514/e2651e7b0be3/molecules-29-05809-g001.jpg

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