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Synthesis and antitumor activities of glucan derivatives

机译:葡聚糖衍生物的合成及其抗肿瘤活性

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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.
机译:一种高效实用的制备β-D-Glc-(1-> 6)-[β-D-Glc-(1-> 3)]-β-D-Glc-(1-描述了> 6)-β-D-Glc-(1→6)-[β-D-Glc-(1→3)]-D-Glc-OMe。还合成了树突状的九糖。根据小鼠肉瘤180的研究,初步研究了六糖,树状大分子,其硫酸化衍生物以及天然葡聚糖蛋白和从灰树花的菌丝体中分离出的相应多糖的抗肿瘤活性。我们的结果表明,与母体糖残基(寡糖或多糖)相比,硫酸化的分支寡糖和天然糖蛋白具有更好的抗肿瘤活性。 (C)2004 Elsevier Ltd.保留所有权利。

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