Synthesis and Biological Evaluation of Novel 4-(4-Formamidophenylamino)-N-methylpicolinamide Derivatives as Potential Antitumor Agents

被引:0
|
作者
Meng, Nana [1 ,2 ,3 ,4 ]
Zhou, Shuyan [1 ,2 ,3 ]
Hu, Min [5 ]
Xu, Youzhi [1 ,2 ,3 ]
Xia, Yong [1 ,2 ,3 ]
Zeng, Xiuxiu [1 ,2 ,3 ]
Yu, Luoting [1 ,2 ,3 ]
机构
[1] Sichuan Univ, State Key Lab Biotherapy, West China Hosp, West China Med Sch, Chengdu 610041, Peoples R China
[2] Sichuan Univ, Canc Ctr, West China Hosp, West China Med Sch, Chengdu 610041, Peoples R China
[3] Collaborat Innovat Ctr, Chengdu 610041, Peoples R China
[4] Sichuan Hairong Pharmaceut Co Ltd, Yangtze River Pharmaceut Grp, Hairong Res Inst, Chengdu 611830, Peoples R China
[5] Sichuan Univ, Open Lab, West China Inst Women & Childrens Hlth, West China Univ Hosp 2, Chengdu 610041, Peoples R China
来源
MOLECULES | 2021年 / 26卷 / 04期
关键词
4-(4-formamidophenylamino)-N-methylpicolinamide derivatives; anti-proliferation; angiogenesis inhibitors; apoptosis; pharmacology;
D O I
10.3390/molecules26041150
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A novel series of 4-(4-formamidophenylamino)-N-methylpicolinamide derivatives were synthesized and evaluated against different tumor cell lines. Experiments in vitro showed that these derivatives could inhibit the proliferation of two kinds of human cancer cell lines (HepG2, HCT116) at low micromolar concentrations and the most potent analog 5q possessed broad-spectrum antiproliferative activity. Experiments in vivo demonstrated that 5q could effectively prolong the longevity of colon carcinoma-burdened mice and slow down the progression of cancer cells by suppression of angiogenesis and the induction of apoptosis and necrosis.
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页数:12
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