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亚氨基糖作为糖基转移酶抑制剂。

Iminosugars as glycosyltransferase inhibitors.

机构信息

Institut des Biomolécules Max Mousseron (IBMM), UMR 5247, CNRS, Université de Montpellier, Ecole Nationale Supérieure de Chimie de Montpellier, 8 Rue de l'Ecole Normale, 34296 Montpellier cedex 5, France.

出版信息

Org Biomol Chem. 2021 Jun 30;19(25):5439-5475. doi: 10.1039/d1ob00382h.

Abstract

Iminosugars are naturally occurring carbohydrate analogues known since 1967. These natural compounds and hundreds of their synthetic derivatives prepared over five decades have been mainly exploited to inhibit the glycosidases, the enzymes catalysing the glycosidic bond cleavage, in order to find new drugs for the treatment of type 2 diabetes and other diseases. However, iminosugars are also inhibitors of glycosyltransferases, the enzymes responsible for the synthesis of oligosaccharides and glycoconjugates. The selective inhibition of specific glycosyltransferases involved in cancer or bacterial infections could lead to innovative therapeutic agents. The synthesis and biological properties of all the iminosugars assayed to date as glycosyltransferase inhibitors are reviewed in the present article.

摘要

亚氨基糖是自 1967 年以来已知的天然存在的碳水化合物类似物。这些天然化合物及其在过去五十年中制备的数百种合成衍生物主要被用于抑制糖苷酶,即催化糖苷键断裂的酶,以寻找治疗 2 型糖尿病和其他疾病的新药。然而,亚氨基糖也是糖基转移酶的抑制剂,糖基转移酶负责寡糖和糖缀合物的合成。特异性抑制参与癌症或细菌感染的特定糖基转移酶可能会导致创新的治疗药物。本文综述了迄今为止作为糖基转移酶抑制剂进行测试的所有亚氨基糖的合成和生物学特性。

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