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Design, synthesis and biological evaluation of chrysin benzimidazole derivatives as potential anticancer agents

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成果类型:
期刊论文
作者:
Wang, Zhe;Deng, Xiangping;Xiong, Shujuan;Xiong, Runde;Liu, Juan;...
通讯作者:
Zheng, Xing;Tang, Guotao
作者机构:
[Wang, Zhe; Liu, Yunmei; Zou, Liu; Liu, Juan; Zheng, X; Tang, GT; Tang, Guotao; Zheng, Xing; Deng, Xiangping; Xie, Zhizhong; Lei, Xiaoyong; Xiong, Shujuan; Xiong, Runde; Cao, Xuan] Univ South China, Hunan Prov Cooperat Innovat Ctr Mol Target New Dr, Inst Pharm & Pharmacol, Hengyang, Peoples R China.
[Chen, Yanming] Mu Dan Jiang You Bo Pharmacert Co Ltd, Mudanjiang, Peoples R China.
通讯机构:
[Zheng, X; Tang, GT] U
Univ South China, Hunan Prov Cooperat Innovat Ctr Mol Target New Dr, Inst Pharm & Pharmacol, Hengyang, Peoples R China.
语种:
英文
关键词:
Chrysin;benzimidazole;synthesis;anticancer
期刊:
Natural Product Research
ISSN:
1478-6419
年:
2018
卷:
32
期:
24
页码:
2900-2909
基金类别:
Construct Program of the key Discipine in Hunan Province; Hunan Province Cooperative Innovation Center for Molecular Target New Drug
机构署名:
本校为第一且通讯机构
院系归属:
药学与生物科学学院
摘要:
A series of chrysin benzimidazole derivatives were synthesised and evaluated for their anticancer activity in the search for potential anticancer agents. Among them, compound 18 displayed the most potent anti-proliferative activity against MFC cells with IC50 values of 25.72 ± 3.95 μM. The flow cytometry results displayed that compound 18 induced apoptosis of MFC cells in a dose-dependent manner and caused the cell cycle to be arrested in the G0/G1 phase. Furthermore, the preliminary anticancer activity in vivo was also studied in tumour-bear...

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