Busca Patricia, Piller Véronique, Piller Friedrich, Martin Olivier R
Institut de Chimie Organique et Analytique, Université d'Orléans, BP 6759, 45067 Orléans, France.
Bioorg Med Chem Lett. 2003 Jun 2;13(11):1853-6. doi: 10.1016/s0960-894x(03)00287-7.
A series of three O-methylated UDP-GalNAc analogues have been synthesised using a divergent strategy from a 3,6-di-O-pivaloyl GlcNAc derivative. The biological activity of these probes toward polypeptide-alpha-GalNAc-transferase T1 has been investigated. This study shows that this glycosyltransferase exhibits a very high substrate specificity.
使用一种从3,6-二-O-新戊酰基GlcNAc衍生物出发的发散策略合成了一系列三种O-甲基化的UDP-GalNAc类似物。已经研究了这些探针对多肽-α-GalNAc转移酶T1的生物活性。这项研究表明,这种糖基转移酶表现出非常高的底物特异性。