2-Substituted methyl α-d-galactopyranosides: Synthesis and binding affinity for the A and B subunits of the Griffonia simplicifolia I isolectins
作者:Rokuro Kaifu、Lisa C. Plantefaber、Irwin J. Goldstein
DOI:10.1016/0008-6215(85)85047-3
日期:1985.7
The binding affinities of the N-acetyl, N-trifluoroacetyl, N-propionyl, N-formyl, N-benzoyl, N-p-nitrobenzoyl, N-p-aminobenzoyl, and N-methyl derivatives of methyl 2-amino-2-deoxy-alpha-D-galactopyranoside and the 2-O-acetyl, -benzoyl, -benzyl, and -methyl derivatives of methyl alpha-D-galactopyranoside for the A and B subunits of the Griffonia simplicifolia I isolectins have been determined by hapten
N-乙酰基,N-三氟乙酰基,N-丙酰基,N-甲酰基,N-苯甲酰基,Np-硝基苯甲酰基,Np-氨基苯甲酰基和甲基-2-氨基-2-脱氧-α-甲基的N-甲基衍生物的结合亲和力已通过半乳甘露聚糖的半抗原抑制分析确定了D-半乳糖吡喃糖苷和Griffonia simplicifolia I isolectins的A和B亚基的甲基α-D-半乳糖吡喃糖苷的2-O-乙酰基,-苯甲酰基,-苄基和-甲基衍生物-isolectin沉淀系统。这些糖-蛋白质相互作用的模型与基于电子和空间效应的结果解释一起提供。