Synthesis and antitumor activities of glucan derivatives

被引:17
作者
Du, YG [1 ]
Gu, GF
Hua, YX
Wei, GH
Ye, XS
Yu, GL
机构
[1] Chinese Acad Sci, Ecoenvironm Sci Res Ctr, Beijing 100085, Peoples R China
[2] Peking Univ, Sch Pharmaceut Sci, State Key Lab Nat & Biomimet Drug, Beijing 100083, Peoples R China
[3] Ocean Univ China, Inst Marine Drug & Food, Qingdao 266003, Peoples R China
基金
中国国家自然科学基金;
关键词
carbohydrates; glycosylations; antitumor agents; glycodendrimers; oligosaccharides;
D O I
10.1016/j.tet.2004.05.086
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A highly efficient and practical method for the preparation of beta-D-Glc-(1-->6)-[beta-D-Glc-(1-->3)]-beta-D-Glc-(1-->6)-beta-D-Glc-(1-->6)-[beta-D-Glc-(1-->3)]-D-Glc-OMe was described. A dendritic nonasaccharide was also synthesized. The antitumor activities of hexasaccharide, the dendrimer, their sulfated derivatives, together with the natural glucan-protein and the corresponding polysaccharide isolated from barmy mycelium of Grifola frondosa, were preliminarily investigated based on Sarcoma-180 studies in mice tests. Our results suggest that the sulfated branching oligosaccharide and natural glycoprotein have better antitumor activities comparing to the parent sugar residue (oligosaccharide or polysaccharide). (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6345 / 6351
页数:7
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