Synthesis of 2′-C-methylcytidine and 2′-C-methyluridine derivatives modified in the 3′-position as potential antiviral agents

被引:13
|
作者
Pierra, Claire
Amador, Agnes
Badaroux, Eric
Storer, Richard
Gosselin, Gilles
机构
[1] Univ Montpellier 2, CNRS, Lab Cooperatif Idenix, F-34095 Montpellier 5, France
[2] Labs Idenix SARL, Lab Chim Med, Cap Gamma, F-34189 Montpellier, France
关键词
pyrimidines; antivirals; hepatitis C virus; 2 '-C-methyl branched ribonucleosides; deoxygenation; fluorination; RNA viruses; nucleosides;
D O I
10.1135/cccc20060991
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
As part of our anti-hepatitis C program, we recently discovered 2'-C-methylcytidine ( 1) and 2'-C-methyluridine ( 2), which are potent inhibitors in cell culture of several viruses ( bovine viral diarrhea virus ( BVDV), yellow fever virus (YFV)) closely related to HCV. In order to characterize structure - activity relationships, we introduced some structural and functional modifications into the 3'-position of 2'-C-methylcytidine and 2'-C-methyluridine. All these hitherto unknown compounds thus synthesized were tested for the activity against a wide range of viruses and found to be inactive.
引用
收藏
页码:991 / 1010
页数:20
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