SYNTHESIS OF 4-EPI-2-DEOXY-2-H-EQ-N-ACETYLNEURAMINIC ACID AND 2,4-DIDEOXY-2-H-EQ-N-ACETYLNEURAMINIC ACID

被引:4
作者
BANDGAR, BP [1 ]
ZBIRAL, E [1 ]
机构
[1] UNIV VIENNA,INST ORGAN CHEM,A-1090 VIENNA,AUSTRIA
关键词
4-EPI-2-DEOXY-2-H-EQ-N-ACETYLNEURAMINIC ACID 2,4-DIDEOXY-2-H-EQ-N-ACETYLNEURAMINIC ACID;
D O I
10.1016/0008-6215(95)00013-J
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
We have continued our work to develop novel analogues of sialic acid [1-4] that may specifically modulate the interaction between endogenous sialic acid and influenza virus haemagglutinin [3,5,6]. Functional groups of sialic acid that have been implicated for this virus-host recongnition are the glycerol side chain, N-acetyl group and the axially oriented carboxylic acid function [3]. In this report we describe the synthesis of two analogues, namely, 4-epi-2-deoxy-2-H-eq-N-acetylneuraminic acid (4-epi-2-d-2-H-eq-Neu5Ac) and 2,4-dideoxy-2-H-eq-N-acetylneuraminic acid (2,4-d(2)-2-H-eq-Neu5Ac).
引用
收藏
页码:201 / 210
页数:10
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