• 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

新型δ2-1,2,4-恶二唑啉衍生物的合成及其体外抗HIV活性

Synthesis and in vitro anti-HIV activity of novel delta 2-1,2,4-oxadiazoline derivatives.

作者信息

Chimirri A, Grasso S, Monforte A M, Monforte P, Zappalà M, Carotti A

机构信息

Dipartimento Farmaco-Chimico, Università di Messina, Italy.

出版信息

Farmaco. 1994 Jul-Aug;49(7-8):509-11.

PMID:7945718
Abstract

The synthesis of 4-adamantyl-5-aryl-3-phenyl-delta 2-1,2,4-oxadiazolines, involving an 1,3-dipolar cycloaddition reaction between 1-[(arylidene)amino]adamantanes and benzonitriloxide, is described. The evaluation of in vitro antiviral activity against human immunodeficiency virus (HIV) of the compounds obtained is also reported.

摘要

描述了4-金刚烷基-5-芳基-3-苯基-Δ2-1,2,4-恶二唑啉的合成,该合成涉及1-[(亚芳基)氨基]金刚烷与苯甲腈氧化物之间的1,3-偶极环加成反应。还报道了所获得化合物对人类免疫缺陷病毒(HIV)的体外抗病毒活性评估。

相似文献

1
Synthesis and in vitro anti-HIV activity of novel delta 2-1,2,4-oxadiazoline derivatives.新型δ2-1,2,4-恶二唑啉衍生物的合成及其体外抗HIV活性
Farmaco. 1994 Jul-Aug;49(7-8):509-11.
2
Synthesis, antimicrobial, and anti-HIV-1 activity of certain 5-(1-adamantyl)-2-substituted thio-1,3,4-oxadiazoles and 5-(1-adamantyl)-3-substituted aminomethyl-1,3,4-oxadiazoline-2-thiones.某些5-(1-金刚烷基)-2-取代硫代-1,3,4-恶二唑和5-(1-金刚烷基)-3-取代氨甲基-1,3,4-恶二唑啉-2-硫酮的合成、抗菌及抗HIV-1活性
Bioorg Med Chem. 2004 Oct 1;12(19):5107-13. doi: 10.1016/j.bmc.2004.07.033.
3
Synthesis and antiviral evaluation of some sugar arylglycinoylhydrazones and their oxadiazoline derivatives.某些糖芳基甘氨酰腙及其恶二唑啉衍生物的合成与抗病毒活性评价
Arch Pharm (Weinheim). 2006 Dec;339(12):656-63. doi: 10.1002/ardp.200600100.
4
2-(4-Pyridyl)-delta 2-1,3,4-oxadiazolines from isonicotinoylhydrazones and diazomethane as potential antimycobacterial and anti-HIV agents. V.由异烟酰腙和重氮甲烷制备的2-(4-吡啶基)-δ2-1,3,4-恶二唑啉作为潜在的抗分枝杆菌和抗HIV药物。V.
Farmaco. 1995 Nov;50(11):783-6.
5
Synthesis and antitumor activity evaluation of Delta2-1,2,4-oxadiazoline derivatives.Δ2-1,2,4-恶二唑啉衍生物的合成与抗肿瘤活性评价
Farmaco. 1996 Feb;51(2):125-9.
6
Anti-HIV agents. I: Synthesis and in vitro anti-HIV evaluation of novel 1H,3H-thiazolo[3,4-a]benzimidazoles.抗HIV药物。I:新型1H,3H-噻唑并[3,4-a]苯并咪唑的合成及体外抗HIV活性评价
Farmaco. 1991 Jun;46(6):817-23.
7
Anti-HIV agents. III. Synthesis and in vitro anti-HIV activity of novel 1H,3H-thiazolo[3,4-a]imidazo[4,5-b]pyridines.抗艾滋病病毒药物。III. 新型1H,3H-噻唑并[3,4-a]咪唑并[4,5-b]吡啶的合成及体外抗艾滋病病毒活性
Farmaco. 1994 May;49(5):345-8.
8
Halogenated isoniazid derivatives as possible antimycobacterial and anti-HIV agents--III.卤代异烟肼衍生物作为潜在的抗分枝杆菌和抗艾滋病毒药物——III。
Farmaco. 1994 Dec;49(12):775-81.
9
Synthesis and anti-HIV activity of 10,11-dihydropyrrolo [1,2-b][1,2,5]benzothiadiazepine-11-acetic acid 5,5-dioxide derivatives and related compounds.10,11 - 二氢吡咯并[1,2 - b][1,2,5]苯并噻二氮杂卓 - 11 - 乙酸5,5 - 二氧化物衍生物及相关化合物的合成与抗HIV活性
Farmaco. 1996 Jun;51(6):425-30.
10
Synthesis, QSAR and anti-HIV activity of new 5-benzylthio-1,3,4-oxadiazoles derived from α-amino acids.新型 5-苄基硫代-1,3,4-恶二唑的合成、定量构效关系和抗 HIV 活性研究,这些化合物均来源于α-氨基酸。
J Enzyme Inhib Med Chem. 2011 Oct;26(5):668-80. doi: 10.3109/14756366.2010.546792. Epub 2011 Jan 21.

引用本文的文献

1
Synthesis, antimicrobial and antiviral testing of some new 1-adamantyl analogues.一些新金刚烷类似物的合成、抗菌和抗病毒测试。
Saudi Pharm J. 2010 Jul;18(3):123-8. doi: 10.1016/j.jsps.2010.05.004. Epub 2010 May 31.
2
2-[3-Acetyl-5-(2-chloro-3-pyrid-yl)-2-methyl-2,3-dihydro-1,3,4-oxadiazol-2-yl]-4-fluoro-phenyl acetate.2-[3-乙酰基-5-(2-氯-3-吡啶基)-2-甲基-2,3-二氢-1,3,4-恶二唑-2-基]-4-氟苯基乙酸酯
Acta Crystallogr Sect E Struct Rep Online. 2009 Apr 30;65(Pt 5):o1181. doi: 10.1107/S1600536809015323.