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Design, synthesis, and antitumor evaluation of trimethoxyflavonoid with arylurea structure against hepatocellular carcinoma

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成果类型:
期刊论文
作者:
Sun, Xueyan;Zhao, Yin;Zhao, Jingduo;Xie, Zhizhong;Lei, Xiaoyong;...
通讯作者:
Tang, G.;Wang, Z.
作者机构:
[Xie, Zhizhong; Zhao, Yin; Lei, Xiaoyong; Sun, Xueyan; Zhao, Jingduo; Tang, Guotao] Heng Yang Med Sch, Inst Pharm & Pharmacol, Hunan Prov Key Lab Tumor Microenvironm Respons Dru, Hengyang, Hunan, Peoples R China.
[Li, Yong; Liu, Xingyun] Univ South China, Nanhua Hosp, Hengyang Med Sch, Hengyang, Hunan, Peoples R China.
[Huang, Sheng] Jiuzhitang Co Ltd, Changsha, Hunan, Peoples R China.
[Wang, Zhe] Univ South China, Affiliated Hosp 2, Hengyang Med Sch, Dept Pharm, Hengyang, Hunan, Peoples R China.
[Wang, Zhe] Univ South China, Affiliated Hosp 2, Dept Pharm, Hengyang Med Sch, Hengyang 421001, Hunan, Peoples R China.
通讯机构:
[Zhe Wang] T
[Guotao Tang] I
The Second Affiliated Hospital, Department of Pharmacy, Hengyang Medical School, University of South China, Hunan, Hengyang, China<&wdkj&>Institute of Pharmacy and Pharmacology, Hunan Provincial Key Laboratory of Tumor Microenvironment Responsive Drug Research, HengYang Medicial School, Hengyang, Hunan, China
语种:
英文
关键词:
antitumor;arylurea flavonoid;glycolysis;trimethoxy;tumor vasculature
期刊:
Drug Development Research
ISSN:
0272-4391
年:
2023
卷:
84
期:
3
页码:
406-422
基金类别:
This work was financially supported by Hunan Provincial Key Laboratory of tumor microenvironment responsive drug research (Approval number: 2019‐56), the Natural Science Foundation of Hunan Province (Award Number: 2020JJ4534), Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study, and Tumor Microenvironment Responsive to Natural Product R&D Graduate Innovation Base.
机构署名:
本校为其他机构
院系归属:
药学与生物科学学院
摘要:
Simultaneous targeting of tumor vasculature and inhibitors of tumor cell glycolysis may be a promising antitumor strategy. Here, we reported the total synthesis and biological evaluation of A-ring arylurea flavonoid derivatives with B-ring trimethoxy group, which exhibited potent antitumor activity against a variety of tumor cells in vitro. Most of the derivatives showed in vitro antitumor activity on HepG-2, HGC-27, MDA-MB-231, and A549 cells. Among them, compounds 8e, 8f, 8g, 8h, 8j, and 8l also exhibited significant anti-proliferation effect...

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