Berehe Solomon Girmay, Sileshi Abera Ayele, Syed Azeem Abbas, Su San Jang, Eunhye Jung, Jin Soo Shin, Soo Bong Han and Hyejin Kim
{"title":"针对寨卡病毒感染的新型异噁唑基小分子的发现和结构-活性关系研究","authors":"Berehe Solomon Girmay, Sileshi Abera Ayele, Syed Azeem Abbas, Su San Jang, Eunhye Jung, Jin Soo Shin, Soo Bong Han and Hyejin Kim","doi":"10.1039/D4MD00240G","DOIUrl":null,"url":null,"abstract":"<p >The Zika virus (ZIKV), a significant public health threat, is transmitted by <em>Aedes aegypti</em> mosquitoes and is associated with severe neurological disorders, particularly in newborns. Currently, there are no approved vaccines or specific therapeutics for ZIKV. Our study focuses on the identification and optimization of isoxazole-based small molecules, specifically through the structural modification of <strong>KR-26827</strong>, to combat ZIKV infections. Among the synthesized derivatives, <strong>7l</strong> emerged as the most promising candidate, showing potent antiviral activity against ZIKV strains and an improved safety profile <em>in vitro</em>. This research underlines the potential of <strong>7l</strong> for further development as a ZIKV therapeutic agent.</p>","PeriodicalId":21462,"journal":{"name":"RSC medicinal chemistry","volume":" 8","pages":" 2792-2805"},"PeriodicalIF":4.1000,"publicationDate":"2024-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Discovery and structure–activity relationship study of novel isoxazole-based small molecules targeting Zika virus infections†\",\"authors\":\"Berehe Solomon Girmay, Sileshi Abera Ayele, Syed Azeem Abbas, Su San Jang, Eunhye Jung, Jin Soo Shin, Soo Bong Han and Hyejin Kim\",\"doi\":\"10.1039/D4MD00240G\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The Zika virus (ZIKV), a significant public health threat, is transmitted by <em>Aedes aegypti</em> mosquitoes and is associated with severe neurological disorders, particularly in newborns. Currently, there are no approved vaccines or specific therapeutics for ZIKV. Our study focuses on the identification and optimization of isoxazole-based small molecules, specifically through the structural modification of <strong>KR-26827</strong>, to combat ZIKV infections. Among the synthesized derivatives, <strong>7l</strong> emerged as the most promising candidate, showing potent antiviral activity against ZIKV strains and an improved safety profile <em>in vitro</em>. This research underlines the potential of <strong>7l</strong> for further development as a ZIKV therapeutic agent.</p>\",\"PeriodicalId\":21462,\"journal\":{\"name\":\"RSC medicinal chemistry\",\"volume\":\" 8\",\"pages\":\" 2792-2805\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2024-07-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"RSC medicinal chemistry\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2024/md/d4md00240g\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"RSC medicinal chemistry","FirstCategoryId":"3","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/md/d4md00240g","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Discovery and structure–activity relationship study of novel isoxazole-based small molecules targeting Zika virus infections†
The Zika virus (ZIKV), a significant public health threat, is transmitted by Aedes aegypti mosquitoes and is associated with severe neurological disorders, particularly in newborns. Currently, there are no approved vaccines or specific therapeutics for ZIKV. Our study focuses on the identification and optimization of isoxazole-based small molecules, specifically through the structural modification of KR-26827, to combat ZIKV infections. Among the synthesized derivatives, 7l emerged as the most promising candidate, showing potent antiviral activity against ZIKV strains and an improved safety profile in vitro. This research underlines the potential of 7l for further development as a ZIKV therapeutic agent.