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抗病毒药物掺入病毒DNA的物理和生物学后果。

Physical and biological consequences of incorporation of antiviral agents into virus DNA.

作者信息

Prusoff W H, Mancini W R, Lin T S, Lee J J, Siegel S A, Otto M J

出版信息

Antiviral Res. 1984 Dec;4(6):303-15. doi: 10.1016/0166-3542(84)90001-9.

Abstract

The molecular basis for the antiviral activity is discussed for a variety of nucleoside compounds approved for clinical use in the U.S.A. (5-iodo-2'-deoxyuridine, 5-trifluoromethyl-2'-deoxyuridine, 9-beta-D-arabinofuranosyladenine, 9-(2-hydroxyethoxymethyl)guanine), or in clinical trial (E-5-(2-bromovinyl)-2'-deoxyuridine, 1-(2-deoxy-2-fluoro-beta-D-arabinosyl)-5-iodocytosine, 1-beta-D-ribofuranosyl-1,2,4-triazole-3-carboxamide), or of specific interest to our laboratory (5-iodo-5'-amino-2',5'-dideoxyuridine, 5'-amino-5'-deoxythymidine). The consequence of incorporation of idoxuridine, the 5'-amino analog of thymidine or the 5'-amino analog of idoxuridine into the DNA of herpes simplex virus type 1 on transcription and translation is emphasized.

摘要

本文讨论了多种已获美国批准用于临床(5-碘-2'-脱氧尿苷、5-三氟甲基-2'-脱氧尿苷、9-β-D-阿拉伯呋喃糖基腺嘌呤、9-(2-羟乙氧基甲基)鸟嘌呤)、或正处于临床试验阶段(E-5-(2-溴乙烯基)-2'-脱氧尿苷、1-(2-脱氧-2-氟-β-D-阿拉伯呋喃糖基)-5-碘胞嘧啶、1-β-D-呋喃核糖基-1,2,4-三唑-3-甲酰胺)、或本实验室特别感兴趣的核苷化合物(5-碘-5'-氨基-2',5'-二脱氧尿苷、5'-氨基-5'-脱氧胸苷)的抗病毒活性的分子基础。文中强调了将碘苷、胸苷的5'-氨基类似物或碘苷的5'-氨基类似物掺入单纯疱疹病毒1型DNA中对转录和翻译的影响。

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