Homo-N-nucleosides: Incorporation into oligonucleotides and antiviral activity.

被引:18
作者
Hossain, N [1 ]
Hendrix, C [1 ]
Lescrinier, E [1 ]
VanAerschot, A [1 ]
Busson, R [1 ]
DeClercq, E [1 ]
Herdewijn, P [1 ]
机构
[1] KATHOLIEKE UNIV LEUVEN,REGA INST MED RES,B-3000 LOUVAIN,BELGIUM
关键词
D O I
10.1016/S0960-894X(96)00254-5
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Homo-N-nucleosides can be efficiently synthesized from 2-deoxyribose. When incorporated in an oligonucleotide, the compounds have a detrimental influence on duplex stability and on the catalytic activity of hammerhead ribozymes. However, homo-N-nucleosides with a guanine or adenine base moiety do exhibit selective antiviral activity against herpes simplex virus (HSV-1 and HSV-2). Copyright (C) 1996 Elsevier Science Ltd
引用
收藏
页码:1465 / 1468
页数:4
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