吡啶和异喹啉同二聚体的生物活性

IF 1.5 4区 化学 Q3 CHEMISTRY, ORGANIC
Shunsuke Tanaka , Kaori Ota , Jian-Rong Zhou , Kazumi Yokomizo , Nobuhiro Kashige , Makoto Furutachi
{"title":"吡啶和异喹啉同二聚体的生物活性","authors":"Shunsuke Tanaka ,&nbsp;Kaori Ota ,&nbsp;Jian-Rong Zhou ,&nbsp;Kazumi Yokomizo ,&nbsp;Nobuhiro Kashige ,&nbsp;Makoto Furutachi","doi":"10.1016/j.tetlet.2025.155756","DOIUrl":null,"url":null,"abstract":"<div><div>This study reports the design and synthesis of homodimers incorporating pyridine and isoquinoline units at their termini, referred to as pyridine and isoquinoline homodimers. First, a pyridine homodimer was synthesized in moderate yield using a previously reported pyridin-4-yl counterpart. In contrast, the isoquinoline homodimer—containing two ether linkages and a methylene linker—was obtained in moderate to high yields. The resulting pyridine and isoquinoline homodimers exhibited antibacterial and antiviral activities. Thus, we successfully synthesized pyridine and isoquinoline homodimers <strong>3</strong> and <strong>6</strong> in moderate to high yields and demonstrated their antibacterial or antiviral properties by evaluating their bioactivities.</div></div>","PeriodicalId":438,"journal":{"name":"Tetrahedron Letters","volume":"170 ","pages":"Article 155756"},"PeriodicalIF":1.5000,"publicationDate":"2025-07-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Bioactivity of pyridine and isoquinoline homodimers\",\"authors\":\"Shunsuke Tanaka ,&nbsp;Kaori Ota ,&nbsp;Jian-Rong Zhou ,&nbsp;Kazumi Yokomizo ,&nbsp;Nobuhiro Kashige ,&nbsp;Makoto Furutachi\",\"doi\":\"10.1016/j.tetlet.2025.155756\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>This study reports the design and synthesis of homodimers incorporating pyridine and isoquinoline units at their termini, referred to as pyridine and isoquinoline homodimers. First, a pyridine homodimer was synthesized in moderate yield using a previously reported pyridin-4-yl counterpart. In contrast, the isoquinoline homodimer—containing two ether linkages and a methylene linker—was obtained in moderate to high yields. The resulting pyridine and isoquinoline homodimers exhibited antibacterial and antiviral activities. Thus, we successfully synthesized pyridine and isoquinoline homodimers <strong>3</strong> and <strong>6</strong> in moderate to high yields and demonstrated their antibacterial or antiviral properties by evaluating their bioactivities.</div></div>\",\"PeriodicalId\":438,\"journal\":{\"name\":\"Tetrahedron Letters\",\"volume\":\"170 \",\"pages\":\"Article 155756\"},\"PeriodicalIF\":1.5000,\"publicationDate\":\"2025-07-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Tetrahedron Letters\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0040403925003053\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tetrahedron Letters","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0040403925003053","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0

摘要

本研究报道了末端含有吡啶和异喹啉单元的同型二聚体的设计和合成,称为吡啶和异喹啉同型二聚体。首先,用先前报道的吡啶-4-基对应物以中等产率合成了吡啶同型二聚体。而含两个醚键和一个亚甲基键的异喹啉同二聚体,产率中高。得到的吡啶和异喹啉二聚体具有抗菌和抗病毒活性。因此,我们成功地以中高收率合成了吡啶和异喹啉二聚体3和6,并通过评价它们的生物活性证明了它们的抗菌或抗病毒特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Bioactivity of pyridine and isoquinoline homodimers

Bioactivity of pyridine and isoquinoline homodimers
This study reports the design and synthesis of homodimers incorporating pyridine and isoquinoline units at their termini, referred to as pyridine and isoquinoline homodimers. First, a pyridine homodimer was synthesized in moderate yield using a previously reported pyridin-4-yl counterpart. In contrast, the isoquinoline homodimer—containing two ether linkages and a methylene linker—was obtained in moderate to high yields. The resulting pyridine and isoquinoline homodimers exhibited antibacterial and antiviral activities. Thus, we successfully synthesized pyridine and isoquinoline homodimers 3 and 6 in moderate to high yields and demonstrated their antibacterial or antiviral properties by evaluating their bioactivities.
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
Tetrahedron Letters
Tetrahedron Letters 化学-有机化学
CiteScore
3.50
自引率
5.60%
发文量
521
审稿时长
28 days
期刊介绍: Tetrahedron Letters provides maximum dissemination of outstanding developments in organic chemistry. The journal is published weekly and covers developments in techniques, structures, methods and conclusions in experimental and theoretical organic chemistry. Rapid publication of timely and significant research results enables researchers from all over the world to transmit quickly their new contributions to large, international audiences.
×
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:604180095
Book学术官方微信