{"title":"吡啶和异喹啉同二聚体的生物活性","authors":"Shunsuke Tanaka , Kaori Ota , Jian-Rong Zhou , Kazumi Yokomizo , Nobuhiro Kashige , 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 , Kaori Ota , Jian-Rong Zhou , Kazumi Yokomizo , Nobuhiro Kashige , 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}
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.
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.