INDUCERS OF ENDOGENOUS INTERFERON IN THE SERIES OF 6-ARYLAMINO-PYRIMIDINE-2,4(1H,3H)-DIONES: FROM DESIGN TO PRACTICE

Victor I. Krutikov, A. Erkin, Viktor V. Tetz, I. V. Klaptyuk
{"title":"INDUCERS OF ENDOGENOUS INTERFERON IN THE SERIES OF 6-ARYLAMINO-PYRIMIDINE-2,4(1H,3H)-DIONES: FROM DESIGN TO PRACTICE","authors":"Victor I. Krutikov, A. Erkin, Viktor V. Tetz, I. V. Klaptyuk","doi":"10.36807/1998-9849-2022-63-89-51-57","DOIUrl":null,"url":null,"abstract":"A series of 6-arylaminopyrimidine-2,4(1H,3H)-diones were synthesized via transamination of 6-aminouracil. Among the target compounds, 3-(2,6-dioxo-1,2,3,6-tetrahydropyrimidine-4-yl)aminobenzoic acid methyl ester proved to be an effective endogenous interferon inducer. During biological evaluation followed by a patenting procedure, the ester was assigned the ImmuVag international nonproprietary name.","PeriodicalId":9467,"journal":{"name":"Bulletin of the Saint Petersburg State Institute of Technology (Technical University)","volume":"32 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bulletin of the Saint Petersburg State Institute of Technology (Technical University)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.36807/1998-9849-2022-63-89-51-57","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

A series of 6-arylaminopyrimidine-2,4(1H,3H)-diones were synthesized via transamination of 6-aminouracil. Among the target compounds, 3-(2,6-dioxo-1,2,3,6-tetrahydropyrimidine-4-yl)aminobenzoic acid methyl ester proved to be an effective endogenous interferon inducer. During biological evaluation followed by a patenting procedure, the ester was assigned the ImmuVag international nonproprietary name.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
6-芳基氨基-嘧啶-2,4(1h, 3h)-二酮系列内源性干扰素诱导剂:从设计到实践
以6-氨基尿嘧啶为原料,经转氨化反应合成了一系列6-芳基氨基嘧啶-2,4(1H,3H)二酮。目标化合物中,3 -(2,6-二氧基-1,2,3,6-四氢嘧啶-4-基)氨基苯甲酸甲酯被证明是一种有效的内源性干扰素诱导剂。在随后的生物评估和专利程序中,该酯被授予ImmuVag国际非专利名称。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
PREPARATION TECHNOLOGY OF PLANT-BASED SAUSAGES AND THEIR QUALITY ASSESSMENT MOLECULAR STRUCTURE AND RADIOPROTECTIVE ACTIVITY OF DERIVATIVES OF AMINOETHYLTHIOSULFATES AND AMINOTHIOLS ANALYTICAL QUALITY CONTROL OF ELASTIC EXPLOSIVE MANUFACTURING MECHATRONIC TECHNOLOGICAL COMPLEX AS A DESIGN OBJECT HYDROGEN SULFIDE CORROSION INHIBITORS BASED ON OXYETHYL PIPERAZINE DERIVATIVES
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1