Fluorescent bicyclic furo pyrimidine deoxynucleoside analogs as potent and selective inhibitors of VZV and potential future drugs for the treatment of chickenpox and shingles

被引：35

作者：

McGuigan, C ^{[1
]}

Brancale, A ^{[1
]}

Barucki, H ^{[1
]}

Srinivasan, S ^{[1
]}

Jones, G ^{[1
]}

Pathirana, R ^{[1
]}

Blewett, S ^{[1
]}

Alvarez, R ^{[1
]}

Yarnold, CJ ^{[1
]}

Carangio, A ^{[1
]}

Velázquez, S ^{[1
]}

Andrei, G ^{[1
]}

Snoeck, R ^{[1
]}

De Clercq, E ^{[1
]}

Balzarini, J ^{[1
]}

机构：

[1] Cardiff Univ, Welsh Sch Pharm, Cardiff CF10 3XF, S Glam, Wales

来源：

DRUGS OF THE FUTURE | 2000年 / 25卷 / 11期

关键词：

D O I：

10.1358/dof.2000.025.11.858698

中图分类号：

R9 [药学];

学科分类号：

1007 ;

摘要：

[No abstract available]

引用

页码：1151 / 1161

页数：11

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[45] G/C-modified oligodeoxynucleotides with selective complementarity: Synthesis and hybridization properties [J].

Woo, JS ;

Meyer, RB ;

Gamper, HB .

NUCLEIC ACIDS RESEARCH, 1996, 24 (13) :2470-2475

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