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 IC(50) values of 4.25 μM, 2.65 μM, and 9.95 μM, and A4V-5 with a benzotriazole substitution displayed IC(50) 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 G(2)/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.
Synthesis and screening of novel 2,4-bis substituted quinazolines as tubulin polymerization promoters and antiproliferative agents.
合成和筛选新型 2,4-双取代喹唑啉作为微管蛋白聚合促进剂和抗增殖剂
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作者:Dwivedi Ashish Ranjan, Kumar Vijay, Prashar Vikash, Jangid Kailash, Kumar Naveen, Devi Bharti, Parkash Jyoti, Kumar Vinod
| 期刊: | RSC Medicinal Chemistry | 影响因子: | 3.600 |
| 时间: | 2025 | 起止号: | 2025 Jan 15 |
| doi: | 10.1039/d4md00755g | 研究方向: | 免疫/内分泌 |
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