具有抗炎和抗肿瘤性质的3-芳基-5-十戊基-1,2,4-恶二唑的合成

Natércia M. Miranda Bezerra , Shalom P. De Oliveira, Rajendra M. Srivastava, Joel R. Da Silva
{"title":"具有抗炎和抗肿瘤性质的3-芳基-5-十戊基-1,2,4-恶二唑的合成","authors":"Natércia M. Miranda Bezerra ,&nbsp;Shalom P. De Oliveira,&nbsp;Rajendra M. Srivastava,&nbsp;Joel R. Da Silva","doi":"10.1016/j.farmac.2005.08.003","DOIUrl":null,"url":null,"abstract":"<div><p>A simple, convenient and straightforward synthesis of 3-aryl-1,2,4-oxadiazoles <strong>4a–f</strong> from arylamidoximes <strong>1a–f</strong><span> and palmitic acid </span><strong>2</strong> is described. Compounds <strong>4a–f</strong> are non-lethal in mice at four times the therapeutic dose (i.p., LD<sub>50</sub> <!-->&gt;<!--> <!-->1 g kg<sup>–1</sup><span> of the animals' body weight). These heterocycles have been found to possess antiinflammatory property similar to aspirin and ibuprofen. Three compounds, viz., </span><strong>4a</strong>, <strong>d</strong>, <strong>e</strong><span> have also been evaluated for antitumor activity, where </span><strong>4d</strong><span> exhibited an excellent activity comparable to lapachol.</span></p></div>","PeriodicalId":77128,"journal":{"name":"Farmaco (Societa chimica italiana : 1989)","volume":"60 11","pages":"Pages 955-960"},"PeriodicalIF":0.0000,"publicationDate":"2005-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.farmac.2005.08.003","citationCount":"48","resultStr":"{\"title\":\"Synthesis of 3-aryl-5-decapentyl-1,2,4-oxadiazoles possessing antiinflammatory and antitumor properties\",\"authors\":\"Natércia M. Miranda Bezerra ,&nbsp;Shalom P. De Oliveira,&nbsp;Rajendra M. Srivastava,&nbsp;Joel R. Da Silva\",\"doi\":\"10.1016/j.farmac.2005.08.003\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>A simple, convenient and straightforward synthesis of 3-aryl-1,2,4-oxadiazoles <strong>4a–f</strong> from arylamidoximes <strong>1a–f</strong><span> and palmitic acid </span><strong>2</strong> is described. Compounds <strong>4a–f</strong> are non-lethal in mice at four times the therapeutic dose (i.p., LD<sub>50</sub> <!-->&gt;<!--> <!-->1 g kg<sup>–1</sup><span> of the animals' body weight). These heterocycles have been found to possess antiinflammatory property similar to aspirin and ibuprofen. Three compounds, viz., </span><strong>4a</strong>, <strong>d</strong>, <strong>e</strong><span> have also been evaluated for antitumor activity, where </span><strong>4d</strong><span> exhibited an excellent activity comparable to lapachol.</span></p></div>\",\"PeriodicalId\":77128,\"journal\":{\"name\":\"Farmaco (Societa chimica italiana : 1989)\",\"volume\":\"60 11\",\"pages\":\"Pages 955-960\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2005-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.farmac.2005.08.003\",\"citationCount\":\"48\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Farmaco (Societa chimica italiana : 1989)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0014827X05001758\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Farmaco (Societa chimica italiana : 1989)","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0014827X05001758","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 48

摘要

介绍了一种简单、方便、直接的由芳胺酰肟和棕榈酸2合成3-芳基-1,2,4-恶二唑的方法。化合物4a-f在4倍于治疗剂量时对小鼠无致死性(LD50 >1 g kg(动物体重的1倍)。这些杂环化合物被发现具有类似于阿司匹林和布洛芬的抗炎特性。3种化合物,即4a, d, e也被评估为抗肿瘤活性,其中4d表现出与lapachol相当的优异活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis of 3-aryl-5-decapentyl-1,2,4-oxadiazoles possessing antiinflammatory and antitumor properties

A simple, convenient and straightforward synthesis of 3-aryl-1,2,4-oxadiazoles 4a–f from arylamidoximes 1a–f and palmitic acid 2 is described. Compounds 4a–f are non-lethal in mice at four times the therapeutic dose (i.p., LD50 > 1 g kg–1 of the animals' body weight). These heterocycles have been found to possess antiinflammatory property similar to aspirin and ibuprofen. Three compounds, viz., 4a, d, e have also been evaluated for antitumor activity, where 4d exhibited an excellent activity comparable to lapachol.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信