Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5230022 | Tetrahedron | 2007 | 10 Pages |
Abstract
Two types of aminodisaccharide-nucleoside conjugates were synthesized by the condensation of azidodisaccharide and nucleoside using aliphatic diamine as a linker. The corresponding azidodisaccharides could be yielded from neamine in good yield. The binding properties to 16S RNA of these conjugates were evaluated by SPR. It was found that the nucleobase played a significant role in the binding of these conjugates to 16S RNA and a shorter linker between the aminodisaccharide and nucleoside was favorable for 16S RNA binding.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Li Cai, Qin Li, Bo Ren, Zhen-Jun Yang, Liang-Ren Zhang, Li-He Zhang,