Shaikh Harun A, Sönnichsen Frank D, Lindhorst Thisbe K
Otto Diels Institute of Organic Chemistry, Christiana Albertina University of Kiel, Otto-Hahn-Platz 4, Kiel, Germany.
Carbohydr Res. 2008 Jul 21;343(10-11):1665-74. doi: 10.1016/j.carres.2008.04.015. Epub 2008 Apr 15.
A new type of glycoconjugate mimetic is introduced that combines a glycocluster head group with a peptide part. These 'glycocluster peptides' are designed to serve as mimetics of glycocalyx constituents. A convergent synthetic scheme was followed, consisting of (i) the synthesis of a clustered carbohydrate head group carrying an amino acid at the focal point, and (ii) the solid phase synthesis of the peptide moiety. Finally, peptide coupling on resin furnished two prototype glycocluster peptides, which each exposes three alpha-mannosyl residues in the form of a dendritic wedge, with different conformational features. Extensive purification and NMR studies were necessary to characterize the target compounds and the results of these investigations are reported here together with the synthesis.
引入了一种新型糖缀合物模拟物,它将糖簇头部基团与肽部分结合在一起。这些“糖簇肽”被设计用作糖萼成分的模拟物。采用了一种汇聚合成方案,包括:(i)合成在焦点处带有氨基酸的簇状碳水化合物头部基团,以及(ii)肽部分的固相合成。最后,在树脂上进行肽偶联得到了两种原型糖簇肽,它们各自以树枝状楔形形式暴露三个α-甘露糖基残基,具有不同的构象特征。为了表征目标化合物,进行广泛的纯化和核磁共振研究是必要的,这里报告了这些研究结果以及合成方法。