Discovery of anilinopyrimidine-based naphthamide derivatives as potent VEGFR-2 inhibitors

被引:8
|
作者
Lv, Yongcong [1 ]
Li, Mengyuan [2 ,3 ]
Cao, Sufen [1 ,4 ]
Tong, Linjiang [2 ]
Peng, Ting [2 ]
Wei, Lixin [3 ]
Xie, Hua [2 ]
Ding, Jian [2 ]
Duan, Wenhu [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Mat Med, Dept Med Chem, Shanghai 201203, Peoples R China
[2] Chinese Acad Sci, Div Antitumor Pharmacol, State Key Lab Drug Res, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China
[3] Chinese Acad Sci, Northwest Inst Plateau Biol, Qinghai 81008, Peoples R China
[4] E China Univ Sci & Technol, Sch Pharm, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
ENDOTHELIAL GROWTH-FACTOR; RENAL-CELL CARCINOMA; FACTOR RECEPTOR; KINASE INHIBITORS; ANGIOGENESIS; CANCER; DISEASE;
D O I
10.1039/c5md00191a
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
Vascular endothelial growth factor receptor-2 (VEGFR-2) plays an important role in tumor angiogenesis, and inhibition of the VEGFR-2 signaling pathway has emerged as an attractive strategy for the treatment of cancer. Herein, we describe the design, synthesis, and biological evaluation of anilinopyrimidine-based naphthamide derivatives as potent VEGFR-2 inhibitors. Among the new derivatives, compound 3k exhibited high VEGFR-2 inhibitory potency in both enzymatic and VEGF-induced HUVEC cellular proliferation assays (IC50 = 0.5 and 9.8 nM, respectively). Kinase selectivity profiling revealed that 3k was a highly selective VEGFR-2 inhibitor. Moreover, 3k effectively inhibited angiogenesis in HUVEC tube formation assay.
引用
收藏
页码:1375 / 1380
页数:6
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