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Nucleoside Diphosphate Sugar Analogues that Target Glycosyltransferases

机译:靶向糖基转移酶的核苷二磷酸糖类似物

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摘要

Glycosyltransferases (GTs) are enzymes that transfer carbohydrates to a range of substrates and they play a fundamental role in the recognition processes associated with several diseases. The design of glycomimetics of nucleoside diphosphate (NDP) sugarsthe natural substrates that act as inhibitors or modulators of GTsis not only necessary for the development of glycan-based therapeutic drugs, but is also a crucial tool for understanding their mechanisms of action. Whilst a large number of inhibitors that consist of modifications of the carbohydrate unit and the pyrophosphate linkage have been designed, less attention has been paid to modifications at the ribose moiety and the nucleobase. However, in recent years, promising results have been obtained through such variations, which were prompted by the initial interest in the photolabeling of enzymes to study their structure. In this Focus Review, we survey recent progress in the synthesis of NDP-sugar analogues that are modified at the ribose moiety or at the heterocyclic base.
机译:糖基转移酶(GTs)是将碳水化合物转移到一系列底物上的酶,它们在与几种疾病相关的识别过程中起着基本作用。核苷二磷酸(NDP)糖模拟物的设计是天然底物,它们作为GTsis的抑制剂或调节剂,不仅是开发基于聚糖的治疗药物所必需的,而且还是理解其作用机理的关键工具。尽管已经设计了许多由碳水化合物单元和焦磷酸酯键的修饰组成的抑制剂,但是对核糖部分和核碱基的修饰的关注较少。然而,近年来,通过这种变化已经获得了令人鼓舞的结果,这是由于人们最初对酶的光标记感兴趣以研究其结构而引起的。在本重点综述中,我们调查了在核糖部分或杂环碱基上修饰的NDP糖类似物合成的最新进展。

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