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 , Shalom P. De Oliveira, Rajendra M. Srivastava, 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> <!-->><!--> <!-->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 , Shalom P. De Oliveira, Rajendra M. Srivastava, 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> <!-->><!--> <!-->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。
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.