Synthesis of hyaluronic-acid-related oligosaccharides and analogues, as their 4-methoxyphenyl glycosides, having N-acetyl-β-D-glucosamine at the reducing end

被引:20
作者
Halkes, KM
Slaghek, TM
Hyppönen, TK
Kruiskamp, PH
Ogawa, T
Kamerling, JP
Vliegenthart, JFG
机构
[1] Univ Utrecht, Bijvoet Ctr, Dept Bioorgan Chem, NL-3508 TB Utrecht, Netherlands
[2] DLO, Agrotechnol Res Inst, ATO, NL-6700 AA Wageningen, Netherlands
[3] RIKEN, Inst Phys & Chem Res, Wako, Saitama 35001, Japan
关键词
oxidation; hyaluronic acid oligosaccharides; hyaluronic acid sulfated analogues;
D O I
10.1016/S0008-6215(98)00116-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To contribute to the possibilities to study the ability of oligosaccharide fragments of hyaluronic acid to induce angiogenesis, several hyaluronic-acid-related oligosaccharides and their 6-0-sulfated analogues were synthesised as their 4-methoxyphenyl glycosides having 2-acetamido-2-deoxy-D-glucopyranose at the reducing end. In all syntheses described, the D-glucopyranosyluronic acid residue was obtained by oxidation at C-6 of a corresponding D-glucopyranosyl residue after construction of the oligosaccharide backbone, using pyridinium dichromate and acetic anhydride. (C) 1998 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:161 / 174
页数:14
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