{"title":"新型2,4-二取代喹唑啉类微管蛋白聚合促进剂和抗增殖剂的合成与筛选。","authors":"Ashish Ranjan Dwivedi, Vijay Kumar, Vikash Prashar, Kailash Jangid, Naveen Kumar, Bharti Devi, Jyoti Parkash and Vinod Kumar","doi":"10.1039/D4MD00755G","DOIUrl":null,"url":null,"abstract":"<p >Twelve 2,4-bis-substituted quinazoline-based compounds were synthesized and screened for antiproliferative and tubulin polymerization enhancing potential. In the series, compound <strong>A4V-3</strong> substituted with an imidazole ring displayed IC<small><sub>50</sub></small> values of 4.25 μM, 2.65 μM, and 9.95 μM, and <strong>A4V-5</strong> with a benzotriazole substitution displayed IC<small><sub>50</sub></small> values of 3.45 μM, 7.25 μM, and 8.14 μM against MCF-7, HCT-116 and SHSY-5Y cancer cells, respectively. In the mechanistic studies involving cell cycle analysis, apoptosis assay and JC-1 studies, compound <strong>A4V-3</strong> was found to arrest the cells in the G<small><sub>2</sub></small>/M phase of the cell cycle and induce mitochondria-mediated apoptosis. In addition, compound <strong>A4V-3</strong> displayed significant tubulin polymerization-enhancing potential. 2,4-Bis-substituted quinazoline-based compounds showed appreciable drug-like characteristics and can be developed as potent anticancer agents.</p>","PeriodicalId":21462,"journal":{"name":"RSC medicinal chemistry","volume":" 3","pages":" 1410-1424"},"PeriodicalIF":4.1000,"publicationDate":"2025-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis and screening of novel 2,4-bis substituted quinazolines as tubulin polymerization promoters and antiproliferative agents†\",\"authors\":\"Ashish Ranjan Dwivedi, Vijay Kumar, Vikash Prashar, Kailash Jangid, Naveen Kumar, Bharti Devi, Jyoti Parkash and Vinod Kumar\",\"doi\":\"10.1039/D4MD00755G\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Twelve 2,4-bis-substituted quinazoline-based compounds were synthesized and screened for antiproliferative and tubulin polymerization enhancing potential. In the series, compound <strong>A4V-3</strong> substituted with an imidazole ring displayed IC<small><sub>50</sub></small> values of 4.25 μM, 2.65 μM, and 9.95 μM, and <strong>A4V-5</strong> with a benzotriazole substitution displayed IC<small><sub>50</sub></small> values of 3.45 μM, 7.25 μM, and 8.14 μM against MCF-7, HCT-116 and SHSY-5Y cancer cells, respectively. In the mechanistic studies involving cell cycle analysis, apoptosis assay and JC-1 studies, compound <strong>A4V-3</strong> was found to arrest the cells in the G<small><sub>2</sub></small>/M phase of the cell cycle and induce mitochondria-mediated apoptosis. In addition, compound <strong>A4V-3</strong> displayed significant tubulin polymerization-enhancing potential. 2,4-Bis-substituted quinazoline-based compounds showed appreciable drug-like characteristics and can be developed as potent anticancer agents.</p>\",\"PeriodicalId\":21462,\"journal\":{\"name\":\"RSC medicinal chemistry\",\"volume\":\" 3\",\"pages\":\" 1410-1424\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2025-01-15\",\"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/2025/md/d4md00755g\",\"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/2025/md/d4md00755g","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Synthesis and screening of novel 2,4-bis substituted quinazolines as tubulin polymerization promoters and antiproliferative agents†
Twelve 2,4-bis-substituted quinazoline-based compounds were synthesized and screened for antiproliferative and tubulin polymerization enhancing potential. In the series, compound A4V-3 substituted with an imidazole ring displayed IC50 values of 4.25 μM, 2.65 μM, and 9.95 μM, and A4V-5 with a benzotriazole substitution displayed IC50 values of 3.45 μM, 7.25 μM, and 8.14 μM against MCF-7, HCT-116 and SHSY-5Y cancer cells, respectively. In the mechanistic studies involving cell cycle analysis, apoptosis assay and JC-1 studies, compound A4V-3 was found to arrest the cells in the G2/M phase of the cell cycle and induce mitochondria-mediated apoptosis. In addition, compound A4V-3 displayed significant tubulin polymerization-enhancing potential. 2,4-Bis-substituted quinazoline-based compounds showed appreciable drug-like characteristics and can be developed as potent anticancer agents.