STRUCTURE-ACTIVITY-RELATIONSHIPS OF SIALYL-LEWIS X-CONTAINING OLIGOSACCHARIDES .1. EFFECT OF MODIFICATIONS OF THE FUCOSE MOIETY

被引:90
作者
RAMPHAL, JY [1 ]
ZHENG, ZL [1 ]
PEREZ, C [1 ]
WALKER, LE [1 ]
DEFREES, SA [1 ]
GAETA, FCA [1 ]
机构
[1] CYTEL CORP,DEPT CHEM,SAN DIEGO,CA 92121
关键词
D O I
10.1021/jm00047a003
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Leukocyte adhesion to the vasculature is mediated by E-, P-, and L-selectins. The natural ligands for E- and P-selectins have not been fully characterized but have been shown to contain the tetrasaccharide sialyl Lewis x structure (Sle(x)). To determine the importance of he fucose moiety of SLe(x), various analogs of SLe(x) containing modifications thereof were prepared and tested as inhibitors of E-selectin-mediated cell adhesion. Cellular experiments indicate that replacement of the hydroxyl groups of fucose by hydrogen abrogated E-selectin binding. However, the arabinose analog of fucose (CH3 Delta H) inhibited cell adhesion but was 5-fold less potent than native SLe(x). This data suggests that modifications of fucose on SLe(x) are generally deleterious toward E-selectin binding.
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页码:3459 / 3463
页数:5
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