Synthesis and anti-HCV activity of 2',5'-deoxy-5'-phenacyladenosine analogs.

Masahiro Ikejiri, Takayuki Ohshima, Akemi Fukushima, Kunitada Shimotohno, Tokumi Maruyama
{"title":"Synthesis and anti-HCV activity of 2',5'-deoxy-5'-phenacyladenosine analogs.","authors":"Masahiro Ikejiri,&nbsp;Takayuki Ohshima,&nbsp;Akemi Fukushima,&nbsp;Kunitada Shimotohno,&nbsp;Tokumi Maruyama","doi":"10.1093/nass/nrp052","DOIUrl":null,"url":null,"abstract":"<p><p>Several nucleoside analogs containing a methylene group instead of a 5'-O atom were synthesized to study the effect of the 5'-modification of nucleoside analogs on their anti-HCV activity. Among the analogs, a 5'-phenacyl analog exhibited good anti-HCV activity with an EC(50) of 15.1 muM. This compound is hypothesized to function via a novel type of mechanism that does not involve the conventional 5'-O-triphosphorylation process.</p>","PeriodicalId":87448,"journal":{"name":"Nucleic acids symposium series (2004)","volume":" 53","pages":"103-4"},"PeriodicalIF":0.0000,"publicationDate":"2009-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1093/nass/nrp052","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nucleic acids symposium series (2004)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/nass/nrp052","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Several nucleoside analogs containing a methylene group instead of a 5'-O atom were synthesized to study the effect of the 5'-modification of nucleoside analogs on their anti-HCV activity. Among the analogs, a 5'-phenacyl analog exhibited good anti-HCV activity with an EC(50) of 15.1 muM. This compound is hypothesized to function via a novel type of mechanism that does not involve the conventional 5'-O-triphosphorylation process.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
2',5'-脱氧-5'-苯丙基腺苷类似物的合成及抗hcv活性研究
合成了几种含有亚甲基而非5′-O原子的核苷类似物,研究了核苷类似物的5′修饰对其抗hcv活性的影响。在这些类似物中,5'-phenacyl类似物具有良好的抗hcv活性,EC(50)为15.1 muM。该化合物被假设通过一种不涉及传统5'- o -三磷酸化过程的新型机制起作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Chemical methods to study protein-nucleic acid interactions. Development of novel chemical probes to detect abasic sites in DNA. Assessment of the DNA damage using the fluorescence microscope. Exciton-controlled fluorescence: application to hybridization-sensitive fluorescent DNA probe. Multiple activities of c-di-GMP in Pseudomonas aeruginosa.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1