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新型吡啶甲酰胺基衍生物作为新型VEGFR-2激酶抑制剂的发现:合成、生物学评价及分子对接

Discovery of novel picolinamide-based derivatives as novel VEGFR-2 kinase inhibitors: synthesis, biological evaluation and molecular docking.

作者信息

Sun Wuji, Fang Shubiao, Yan Hong

机构信息

Beijing Key Laboratory of Environmental and Viral Oncology , College of Life Science and Bioengineering , Beijing University of Technology , Pingleyuan Street No. 100, Chaoyang District , Beijing , 100124 , China . Email:

Tong Yi Tang Pharmaceutical Co., Ltd. , Sui'an Industrial Park of Zhangpu County , Fujian Province 363200 , China.

出版信息

Medchemcomm. 2018 May 23;9(6):1054-1058. doi: 10.1039/c8md00057c. eCollection 2018 Jun 1.

DOI:10.1039/c8md00057c
PMID:30108994
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6072080/
Abstract

Vascular endothelial growth factor receptor-2 (VEGFR-2) plays a crucial role in tumor angiogenesis, and inhibition of the VEGFR-2 signaling pathway has emerged as an attractive target for cancer therapy. In our effort, a novel series of picolinamide-based derivatives were designed and synthesized as potent and effective VEGFR-2 inhibitors. All the newly prepared compounds were evaluated for their antiproliferative activity against A549 and HepG2 cell lines. Among the new compounds, and exhibited better activity against both A549 and HepG2 cell lines. Molecular docking was performed to investigate the binding capacity and binding mode with VEGFR-2 (PDB code: ; 4ASD).

摘要

血管内皮生长因子受体-2(VEGFR-2)在肿瘤血管生成中起关键作用,抑制VEGFR-2信号通路已成为癌症治疗的一个有吸引力的靶点。在我们的研究中,设计并合成了一系列新型的基于吡啶甲酰胺的衍生物作为有效的VEGFR-2抑制剂。对所有新制备的化合物进行了针对A549和HepG2细胞系的抗增殖活性评估。在这些新化合物中,[具体化合物名称未给出]对A549和HepG2细胞系均表现出更好的活性。进行了分子对接以研究与VEGFR-2(PDB代码:;4ASD)的结合能力和结合模式。

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