• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

4'-硫代-5-乙基-2'-脱氧尿苷(TEDU)及其衍生物对单纯疱疹病毒所致小鼠实验性感染的疗效

[Efficacy of 4'-thio-5-ethyl-2'-deoxyuridine (TEDU) and its derivatives in experimental infection in mice caused by herpes simplex virus].

作者信息

Andronova V L, Aleksandrova L A, Karpenko I L, Skoblov Iu S

机构信息

D. I. Ivanovsky Institute of Virology, Russian Academy of Medical Sciences, Moscow.

出版信息

Antibiot Khimioter. 2003;48(5):3-6.

PMID:12968461
Abstract

It was demonstrated that several 5'-phosphonates of 4'-thio-5-ethyl-2'-deoxyuridine possessed antiviral activity in vitro and in the murine model of herpes simplex virus type 1 infection. It was shown that the derivatives after intraabdominal administration penetrated effectively into the brain tissue. The agents provided statistically significant increase of the average life span, lower virus titre in the brain and lower lethality when compared to the control group of the animals. It is emphasized that the derivatives were less toxic than the original compound.

摘要

已证明,4'-硫代-5-乙基-2'-脱氧尿苷的几种5'-膦酸酯在体外以及在单纯疱疹病毒1型感染的小鼠模型中具有抗病毒活性。结果表明,腹腔给药后的衍生物能有效渗透到脑组织中。与动物对照组相比,这些药物使平均寿命有统计学意义的增加,降低了脑中的病毒滴度并降低了致死率。需要强调的是,这些衍生物的毒性低于原始化合物。

相似文献

1
[Efficacy of 4'-thio-5-ethyl-2'-deoxyuridine (TEDU) and its derivatives in experimental infection in mice caused by herpes simplex virus].4'-硫代-5-乙基-2'-脱氧尿苷(TEDU)及其衍生物对单纯疱疹病毒所致小鼠实验性感染的疗效
Antibiot Khimioter. 2003;48(5):3-6.
2
[4'-Thio-5-ethyl-2'-deoxyuridine 5'-phosphonates: synthesis and antiviral activity].
Bioorg Khim. 2002 Sep-Oct;28(5):455-61. doi: 10.1023/a:1020476212905.
3
[Antiherpesviral activity of acycloguanosine H-phosphonate in experiments using laboratory animals].
Vopr Virusol. 2011 Sep-Oct;56(5):37-40.
4
DNA polymerase mutations in drug-resistant herpes simplex virus mutants determine in vivo neurovirulence and drug-enzyme interactions.耐药性单纯疱疹病毒突变体中的DNA聚合酶突变决定体内神经毒性和药物-酶相互作用。
Antivir Ther. 2007;12(5):719-32.
5
[Antiherpetic activity of netropsin derivatives as tested in experiments in laboratory animals].[在实验动物实验中测试的纺锤菌素衍生物的抗疱疹活性]
Vopr Virusol. 2012 Jul-Aug;57(4):24-6.
6
[In vitro acyclovir and cidofovir susceptibilities of human herpesvirus type 1 clinical isolates].[人疱疹病毒1型临床分离株的体外阿昔洛韦和西多福韦敏感性]
Med Dosw Mikrobiol. 2008;60(2):163-8.
7
Inhibition of herpes simplex virus type 1 by thymol-related monoterpenoids.香芹酚相关单萜对单纯疱疹病毒 1 的抑制作用。
Planta Med. 2012 Oct;78(15):1636-8. doi: 10.1055/s-0032-1315208. Epub 2012 Aug 13.
8
Antiviral activities against herpes simplex virus type 1 by HPH derivatives and their structure-activity relationships.HPH衍生物对单纯疱疹病毒1型的抗病毒活性及其构效关系。
Bioorg Med Chem Lett. 2008 Jan 1;18(1):371-4. doi: 10.1016/j.bmcl.2007.10.065. Epub 2007 Oct 24.
9
1,2,4-Triazoloazine derivatives as a new type of herpes simplex virus inhibitors.1,2,4-三唑嗪衍生物作为一种新型单纯疱疹病毒抑制剂。
Bioorg Chem. 2010 Dec;38(6):265-70. doi: 10.1016/j.bioorg.2010.09.002. Epub 2010 Sep 22.
10
Phosphoramidate derivatives of acyclovir: synthesis and antiviral activity in HIV-1 and HSV-1 models in vitro.阿昔洛韦的磷酰胺酯衍生物:在 HIV-1 和 HSV-1 模型中的体外抗病毒活性和合成。
Bioorg Med Chem. 2012 Oct 1;20(19):5802-9. doi: 10.1016/j.bmc.2012.08.008. Epub 2012 Aug 17.