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通过化学选择性激活糖基化反应,全合成具有神经突生成活性的神经节苷脂 Hp-s1 类似物。

The total synthesis of a ganglioside Hp-s1 analogue possessing neuritogenic activity by chemoselective activation glycosylation.

机构信息

Department of Chemistry, Chung Yuan Christian University, Chung Li 32023, Taiwan.

出版信息

Org Biomol Chem. 2012 Feb 7;10(5):931-4. doi: 10.1039/c2ob06827c. Epub 2011 Dec 19.

Abstract

The total synthesis of ganglioside 2, an analogue of the ganglioside Hp-s1 (1) which displays neuritogenic activity toward the rat pheochromocytoma cell line PC-12 cell in the presence of nerve growth factor (NGF) with an effect (34.0%) greater than that of the mammalian ganglioside GM 1 (25.4%), was accomplished by applying a chemoselective-activation glycosylation strategy. Moreover, we also demonstrate that the synthesized ganglioside 2 exhibited neuritogenic activity toward the human neuroblastoma cell line SH-SY5Y without the presence of NGF.

摘要

神经节苷脂 2 的全合成,其为神经节苷脂 Hp-s1(1)的类似物,在神经生长因子(NGF)存在的情况下,对大鼠嗜铬细胞瘤 PC-12 细胞具有促神经突生成活性,其效果(34.0%)大于哺乳动物神经节苷脂 GM 1(25.4%),通过应用化学选择性激活糖基化策略来实现。此外,我们还证明合成的神经节苷脂 2 在没有 NGF 的情况下对人神经母细胞瘤 SH-SY5Y 细胞具有促神经突生成活性。

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