Novel polyamide based nucleic acid analogs - Synthesis of oligomers and RNA-binding properties

被引:13
作者
GarciaEcheverria, C
Husken, D
Chiesi, CS
Altmann, KH
机构
[1] CIBA, CENT RES LABS, FRIBOURG, SWITZERLAND
[2] CIBA, DEPT ONCOL, FRIBOURG, SWITZERLAND
关键词
D O I
10.1016/S0960-894X(97)00173-X
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The synthesis of never polyamide based nucleic acid analogs incorporating monomer units of type I - III has been accomplished using solid-phase strategies based on N-delta-Fmoc protected building blocks. An oligomer composed of monomer units I exhibited weak, but sequence-specific RNA binding. Improved RNA-binding affinity was observed for analogs incorporating building blocks of type III with 2-(R) stereochemistry, but nor in the case of the 2-(S) isomers. (C) 1997 Elsevier Science Ltd.
引用
收藏
页码:1123 / 1126
页数:4
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