• 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

Synthesis, antiviral and antiproliferative activity of a new class of 5-(alkyl or arylthio)-6-vinyl uracils.

作者信息

Baraldi P G, Cacciari B, Romagnoli R, Spalluto G, Garuti L, Roberti M, Pani A, Perra G, Scintu F, Pinna N, Musiu C, La Colla P

出版信息

Anticancer Drug Des. 1996 Dec;11(8):597-609.

PMID:9022748
Abstract

Uracil derivatives bearing substituted or unsubstituted vinyl groups at position C6 and alkyl- or arylthio groups at position C5 were synthesized and tested in vitro for antiviral and antiproliferative activity. None of the compounds were active against HIV-1. However, some of them inhibited the proliferation of leukemia, lymphoma and solid tumor-derived cell lines at micromolar concentrations. The maximum potency of antiproliferative activity correlates with the presence of unsubstituted vinyl groups and alkyl- or arylthio substituents.

摘要

相似文献

1
Synthesis, antiviral and antiproliferative activity of a new class of 5-(alkyl or arylthio)-6-vinyl uracils.
Anticancer Drug Des. 1996 Dec;11(8):597-609.
2
Synthesis and antiproliferative activity of 2-triazenothiophenes.2-三氮烯基噻吩的合成及其抗增殖活性
Anticancer Res. 1999 May-Jun;19(3A):2127-31.
3
Synthesis and anti-HIV-1 activity of a series of 1-alkoxy-5-alkyl-6-(arylthio)uracils.一系列1-烷氧基-5-烷基-6-(芳硫基)尿嘧啶的合成及其抗HIV-1活性
J Med Chem. 1997 Jul 18;40(15):2363-73. doi: 10.1021/jm9607921.
4
1,5-Benzodiazepines XIV. Synthesis of new substituted 9H-bis-[1,2,4]triazolo[4,3-a:3',4'-d] [1,5]benzodiazepines and relate compounds endowed with in vitro cytotoxic properties.1,5-苯并二氮杂䓬十四。新型取代的9H-双-[1,2,4]三唑并[4,3-a:3',4'-d][1,5]苯并二氮杂䓬及具有体外细胞毒性特性的相关化合物的合成。
Farmaco. 2005 Feb;60(2):113-25. doi: 10.1016/j.farmac.2004.12.005.
5
Synthesis and antiproliferative activity of some N-sulphonated-2-substituted benzimidazoles and imidazo[4,5-b]pyridines.一些N-磺化-2-取代苯并咪唑和咪唑并[4,5-b]吡啶的合成及其抗增殖活性
Anticancer Drug Des. 1998 Dec;13(8):969-80.
6
Synthesis of novel uracil non-nucleoside derivatives as potential reverse transcriptase inhibitors of HIV-1.合成新型尿嘧啶非核苷衍生物作为 HIV-1 逆转录酶抑制剂的研究。
Arch Pharm (Weinheim). 2009 Nov;342(11):663-70. doi: 10.1002/ardp.200900139.
7
Synthesis of a series of Homopterocarpane derivatives with potential antitumor and anti-AIDS activity.一系列具有潜在抗肿瘤和抗艾滋病活性的高异羽扇豆烷衍生物的合成。
Farmaco. 1997 Jan;52(1):13-9.
8
Synthesis and antiviral activity of 1-substituted 3-(3,5-dimethylbenzyl)uracil against HIV-1.1-取代-3-(3,5-二甲基苄基)尿嘧啶对HIV-1的合成及抗病毒活性
Nucleic Acids Symp Ser (Oxf). 2004(48):3-4. doi: 10.1093/nass/48.1.3.
9
In-vitro anti-HIV and antitumor activity of new 3,6-disubstituted [1,2,4]triazolo[3,4-b][1,3,4]thiadiazoles and thiadiazine analogues.新型3,6-二取代[1,2,4]三唑并[3,4-b][1,3,4]噻二唑及噻二嗪类似物的体外抗HIV和抗肿瘤活性
Arch Pharm (Weinheim). 2008 Jun;341(6):365-9. doi: 10.1002/ardp.200700272.
10
Geometrically and conformationally restrained cinnamoyl compounds as inhibitors of HIV-1 integrase: synthesis, biological evaluation, and molecular modeling.作为HIV-1整合酶抑制剂的几何和构象受限肉桂酰化合物:合成、生物学评价及分子模拟
J Med Chem. 1998 Oct 8;41(21):3948-60. doi: 10.1021/jm9707232.