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三糖甾体皂苷的简明合成及抗肿瘤活性。

Concise synthesis and antitumor activities of trisaccharide steroidal saponins.

机构信息

National Glycoengineering Research Center, Shandong University, Jinan 250100, PR China.

出版信息

Carbohydr Res. 2011 Nov 8;346(15):2406-13. doi: 10.1016/j.carres.2011.08.026. Epub 2011 Sep 1.

Abstract

The naturally derived trisaccharide steroidal saponin 1 and structurally modified derivatives 2 and 3 bearing the same sarsasapogenin aglycon were synthesized concisely via a direct transglycosylation strategy. The antitumor activities of the synthetic trisaccharide saponins 1-3 and their corresponding α-isomers 1a-3a were preliminarily evaluated against human gastric adenocarcinoma cell (MKN-45) and human epithelial cervical cancer cell (HeLa) by CCK-8 assay.

摘要

通过直接糖基化策略,简洁地合成了具有相同薯蓣皂甙元糖苷配基的天然衍生的三糖甾体皂苷 1 及其结构修饰的衍生物 2 和 3。通过 CCK-8 法初步评价了合成的三糖皂苷 1-3 及其相应的α-异构体 1a-3a 对人胃腺癌细胞(MKN-45)和人宫颈癌细胞(HeLa)的抗肿瘤活性。

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