奎宁酸二咖啡酯和二烯丙酯抗hsv -1及抗氧化活性

Celso O. Rezende Jr. , Caroline Rigotto , Wiliam Caneschi , Carlos A.M. Rezende , Mireille Le Hyaric , Mara R.C. Couri , Cláudia M.O. Simões , Mauro V. de Almeida
{"title":"奎宁酸二咖啡酯和二烯丙酯抗hsv -1及抗氧化活性","authors":"Celso O. Rezende Jr. ,&nbsp;Caroline Rigotto ,&nbsp;Wiliam Caneschi ,&nbsp;Carlos A.M. Rezende ,&nbsp;Mireille Le Hyaric ,&nbsp;Mara R.C. Couri ,&nbsp;Cláudia M.O. Simões ,&nbsp;Mauro V. de Almeida","doi":"10.1016/j.bionut.2013.09.007","DOIUrl":null,"url":null,"abstract":"<div><p><span><span>Nine caffeic and gallic acids derivatives were synthesized and evaluated for their antioxidant activity using the </span>DPPH radical scavenging activity assay and for their antiherpes activity against HSV-1. All compounds displayed higher antioxidant activities than α-tocopherol. The most active antioxidant was compound </span><strong>8</strong> (IC<sub>50</sub> <!-->=<!--> <!-->177<!--> <!-->μM). Five compounds (<strong>7, 10, 11, 12</strong> and <strong>14</strong><span>) were found to possess anti-HSV-1 activity with selectivity indices values ranging from 7.0 to 27.1. The most active was compound </span><strong>10</strong> (IC<sub>50</sub> <!-->=<!--> <!-->15.2<!--> <!-->μM; SI<!--> <!-->=<!--> <!-->27.1).</p></div>","PeriodicalId":100182,"journal":{"name":"Biomedicine & Preventive Nutrition","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.bionut.2013.09.007","citationCount":"9","resultStr":"{\"title\":\"Anti-HSV-1 and antioxidant activities of dicaffeoyl and digalloyl esters of quinic acid\",\"authors\":\"Celso O. Rezende Jr. ,&nbsp;Caroline Rigotto ,&nbsp;Wiliam Caneschi ,&nbsp;Carlos A.M. Rezende ,&nbsp;Mireille Le Hyaric ,&nbsp;Mara R.C. Couri ,&nbsp;Cláudia M.O. Simões ,&nbsp;Mauro V. de Almeida\",\"doi\":\"10.1016/j.bionut.2013.09.007\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><span><span>Nine caffeic and gallic acids derivatives were synthesized and evaluated for their antioxidant activity using the </span>DPPH radical scavenging activity assay and for their antiherpes activity against HSV-1. All compounds displayed higher antioxidant activities than α-tocopherol. The most active antioxidant was compound </span><strong>8</strong> (IC<sub>50</sub> <!-->=<!--> <!-->177<!--> <!-->μM). Five compounds (<strong>7, 10, 11, 12</strong> and <strong>14</strong><span>) were found to possess anti-HSV-1 activity with selectivity indices values ranging from 7.0 to 27.1. The most active was compound </span><strong>10</strong> (IC<sub>50</sub> <!-->=<!--> <!-->15.2<!--> <!-->μM; SI<!--> <!-->=<!--> <!-->27.1).</p></div>\",\"PeriodicalId\":100182,\"journal\":{\"name\":\"Biomedicine & Preventive Nutrition\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2014-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.bionut.2013.09.007\",\"citationCount\":\"9\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biomedicine & Preventive Nutrition\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2210523913000639\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomedicine & Preventive Nutrition","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2210523913000639","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 9

摘要

合成了9种咖啡酸和没食子酸衍生物,并利用DPPH自由基清除活性测定法评估了它们的抗氧化活性和对HSV-1的抗疱疹活性。所有化合物的抗氧化活性均高于α-生育酚。化合物8的抗氧化活性最高(IC50 = 177 μM)。5个化合物(7、10、11、12和14)具有抗hsv -1活性,选择性指数在7.0 ~ 27.1之间。活性最高的是化合物10 (IC50 = 15.2 μM;si = 27.1)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anti-HSV-1 and antioxidant activities of dicaffeoyl and digalloyl esters of quinic acid

Nine caffeic and gallic acids derivatives were synthesized and evaluated for their antioxidant activity using the DPPH radical scavenging activity assay and for their antiherpes activity against HSV-1. All compounds displayed higher antioxidant activities than α-tocopherol. The most active antioxidant was compound 8 (IC50 = 177 μM). Five compounds (7, 10, 11, 12 and 14) were found to possess anti-HSV-1 activity with selectivity indices values ranging from 7.0 to 27.1. The most active was compound 10 (IC50 = 15.2 μM; SI = 27.1).

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