Design, synthesis, and antiproliferative activity of novel 1,2,4-triazole-chalcone compounds

被引:0
作者
Li, Jinjing [1 ,2 ]
Fan, Pingping [2 ]
Liu, Yuxiao [2 ]
Zhao, Yan [2 ]
Shi, Chengyang [2 ]
Zhou, Shujing [1 ]
Qiu, Hongbin [2 ]
机构
[1] Jiamusi Univ, Inst Pharm Heilongjiang Prov, Coll Pharm, Jiamusi 154007, Peoples R China
[2] Jiamusi Univ, Coll Pharm, Jiamusi 154007, Peoples R China
基金
黑龙江省自然科学基金;
关键词
chalcone; triazol; molecular hybridization; anti-proliferative activity; CHALCONE DERIVATIVES; INHIBITORS;
D O I
10.1515/hc-2022-0165
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A series of novel 1,2,4-triazole-chalcone compounds 10a-10s were designed by molecular hybridization strategy and synthesized. The molecular structures of the novel chalcones were characterized by H-1-NMR, C-13-NMR, and HRMS. The anti-proliferative activities of the novel chalcones against four cancer cell lines in vitro were examined by MTT, four tumor cell lines including human colon cancer cell SW620, human non-small cell lung cancer cell A549, human cervical cancer cell HeLa, and human breast cancer cell MCF-7. Compound 10o showed certain selectivity to SW620 cell line, and its IC50 value was 21.55 mu M. 10q had good anti-proliferative activity against A549 cells with an IC50 value of 25.58 mu M.
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页数:9
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