氨基丙醇-2金刚烷基(烷基、环烷基)衍生物抗流感作用的体内外研究

O. Voloshchuk, Y. V. Korotkiy, S. Rybalko, D. Starosila, V. Shirobokov
{"title":"氨基丙醇-2金刚烷基(烷基、环烷基)衍生物抗流感作用的体内外研究","authors":"O. Voloshchuk, Y. V. Korotkiy, S. Rybalko, D. Starosila, V. Shirobokov","doi":"10.7124/bc.000968","DOIUrl":null,"url":null,"abstract":"Aim. To establish anti-influenza activities for 8 compounds of adamantyl (alkyl, cycloalkyl) derivatives of aminopropanol-2 in vitro and in vivo investigations. Methods. The antiviral action of compounds was determined in vitro by reduction of infectious titer of the influenza virus in the Madin-Darby Canine Kidney (MDCK) cell culture and in vivo on the model of influenza pneumonia in mice. Results. Three of eight studied compounds inhibit the reproduction of the influenza virus strain A/FM/1/47(H1N1) by more than 2 lg ID 50 in the concentration range from < 0.39 µg/ml (the compounds 30 and 33) to 1.56 µg/ml (the compound 5), their chemotherapeutic indices are 256 and 16, respectively. The experiments in vivo showed that in prophylactic scheme the efficiency index (EI) of the compounds 5 and 30 is 60 %; in therapeutic scheme EI of the compounds 5 and 33 is 100 % that is two times higher, than for rimantadine. Conclusions. High chemotherapeutic indices of the compounds 30, 33 and their ability to sup-press the influenza virus reproduction in the MDCK cell culture by more than 2 lg ID 50 indicate the anti-influenza activity of these compounds. It has been also confirmed by in vivo experiment.","PeriodicalId":9017,"journal":{"name":"Biopolymers & Cell","volume":"10 1","pages":"453-462"},"PeriodicalIF":0.0000,"publicationDate":"2018-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"In vitro and in vivo investigations on anti-influenza effect of adamantyl (alkyl, cycloalkyl) derivatives of aminopropanol-2\",\"authors\":\"O. Voloshchuk, Y. V. Korotkiy, S. Rybalko, D. Starosila, V. Shirobokov\",\"doi\":\"10.7124/bc.000968\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Aim. To establish anti-influenza activities for 8 compounds of adamantyl (alkyl, cycloalkyl) derivatives of aminopropanol-2 in vitro and in vivo investigations. Methods. The antiviral action of compounds was determined in vitro by reduction of infectious titer of the influenza virus in the Madin-Darby Canine Kidney (MDCK) cell culture and in vivo on the model of influenza pneumonia in mice. Results. Three of eight studied compounds inhibit the reproduction of the influenza virus strain A/FM/1/47(H1N1) by more than 2 lg ID 50 in the concentration range from < 0.39 µg/ml (the compounds 30 and 33) to 1.56 µg/ml (the compound 5), their chemotherapeutic indices are 256 and 16, respectively. The experiments in vivo showed that in prophylactic scheme the efficiency index (EI) of the compounds 5 and 30 is 60 %; in therapeutic scheme EI of the compounds 5 and 33 is 100 % that is two times higher, than for rimantadine. Conclusions. High chemotherapeutic indices of the compounds 30, 33 and their ability to sup-press the influenza virus reproduction in the MDCK cell culture by more than 2 lg ID 50 indicate the anti-influenza activity of these compounds. It has been also confirmed by in vivo experiment.\",\"PeriodicalId\":9017,\"journal\":{\"name\":\"Biopolymers & Cell\",\"volume\":\"10 1\",\"pages\":\"453-462\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-01-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biopolymers & Cell\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.7124/bc.000968\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biopolymers & Cell","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.7124/bc.000968","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

摘要

的目标。目的建立氨基丙醇-2金刚烷基(烷基、环烷基)衍生物8个化合物的体外和体内抗流感活性。方法。体外通过降低Madin-Darby犬肾(MDCK)细胞培养中流感病毒的感染滴度和体内对小鼠流感肺炎模型的抗病毒作用来确定化合物的抗病毒作用。结果。8种化合物中有3种在浓度范围< 0.39µg/ml(化合物30和33)至1.56µg/ml(化合物5)范围内对甲型H1N1流感病毒株A/FM/1/47(H1N1)的增殖抑制作用大于2 lgid50,其化疗指数分别为256和16。体内实验表明,化合物5和30在预防方案中的效率指数(EI)为60%;在治疗方案中,化合物5和33的EI为100%,是金刚乙胺的两倍。结论。化合物30,33的高化疗指数及其在MDCK细胞培养中抑制流感病毒繁殖的能力超过2lgid50,表明这些化合物具有抗流感活性。体内实验也证实了这一点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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
In vitro and in vivo investigations on anti-influenza effect of adamantyl (alkyl, cycloalkyl) derivatives of aminopropanol-2
Aim. To establish anti-influenza activities for 8 compounds of adamantyl (alkyl, cycloalkyl) derivatives of aminopropanol-2 in vitro and in vivo investigations. Methods. The antiviral action of compounds was determined in vitro by reduction of infectious titer of the influenza virus in the Madin-Darby Canine Kidney (MDCK) cell culture and in vivo on the model of influenza pneumonia in mice. Results. Three of eight studied compounds inhibit the reproduction of the influenza virus strain A/FM/1/47(H1N1) by more than 2 lg ID 50 in the concentration range from < 0.39 µg/ml (the compounds 30 and 33) to 1.56 µg/ml (the compound 5), their chemotherapeutic indices are 256 and 16, respectively. The experiments in vivo showed that in prophylactic scheme the efficiency index (EI) of the compounds 5 and 30 is 60 %; in therapeutic scheme EI of the compounds 5 and 33 is 100 % that is two times higher, than for rimantadine. Conclusions. High chemotherapeutic indices of the compounds 30, 33 and their ability to sup-press the influenza virus reproduction in the MDCK cell culture by more than 2 lg ID 50 indicate the anti-influenza activity of these compounds. It has been also confirmed by in vivo experiment.
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
期刊最新文献
"Green" synthesis of metal nanoparticles. Application and future perspective Key models and theories of carcinogenesis Alterations in S6K1 isoforms expression induce Epithelial to Mesenchymal Transition and Estrogen Receptor 1 Silencing in human breast adenocarcinoma MCF-7 cells Variation in highly repetitive DNA composition in rye and wild relatives discovered by FISH Effects of transplantation of preconditioned mesenchymal stem cells seeded on a biomimetic 3D scaffold
×
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