SYNTHESES OF 5'-SUBSTITUTED ANALOGS OF CARBOCYCLIC 3-DEAZAADENOSINE AS POTENTIAL ANTIVIRALS

被引:8
|
作者
SECRIST, JA
COMBER, RN
GRAY, RJ
GILROY, RB
MONTGOMERY, JA
机构
[1] Organic Chemistry Department, Southern Research Institute, Birmingham, Alabama 35255-5305
关键词
D O I
10.1021/jm00067a008
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Various 5'-substituted derivatives (2,3,6a, 6b, 9a, 9b, 12,13b, and 15) of carbocyclic 3-deazaadenosine (3-deaza CAdo, 1) were prepared from 3-deaza CAdo (1) and evaluated as antiviral agents against a number of viruses, including HIV-1. Several of the compounds had moderate to good antiviral activity against vaccinia (VV) and vesicular stomatitis (VSV) viruses; however, the antiviral activity of the analogues did not exceed that of the parent compound. No anti-HIV activity was detected.
引用
收藏
页码:2102 / 2106
页数:5
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