中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Research progress in VEGFR-2 inhibitors

文献类型:期刊论文

作者Liu Peng; Zhou Yunfei; Zhang Yong; Wang Guimin; Chen Zhaoqiang; Li Bo; Xu Zhijian; Zhu Weiliang
刊名Acta Pharmaceutica Sinica
出版日期2017
卷号52期号:4页码:531-540
关键词VEGFR-2 VEGFR-2 inhibitors tumor selectivity
ISSN号0513-4870
其他题名VEGFR-2抑制剂研究进展
文献子类Review
英文摘要Vascular endothelial growth factor receptor (VEGFR-2), a member of the super family of protein tyrosine kinase receptors, plays a vital role in the regulation of tumor metastasis and angiogenesis. Several VEGFR-2 inhibitors have been marketed as antitumor drugs and a range of inhibitors are undergoing clinical or preclinical studies. According to the principle of multi-targeted pharmacolgy, in the field of tumor treatment, nonselective drugs targeting on more than one kinase to inhibit different cell pathways can be more effective than drugs specific for one kinase. Multi-target treatment does not mean abandonment of selectivity, but a precise selectivity for several kinases related to tumor, which is also a big challenge in the development of small molecular antitumor drugs. This paper reviews briefly the advances in research of the VEGFR-2 inhibitors and selectivity strategy in recent years.
资助项目上海市扬帆计划资助项目[00000000]
WOS研究方向Pharmacology & Pharmacy (provided by Clarivate Analytics)
语种中文
CSCD记录号CSCD:5955467
源URL[http://119.78.100.183/handle/2S10ELR8/269211]  
专题药物发现与设计中心
通讯作者Zhu Weiliang
作者单位ACS Key Laboratory of Receptor Research,Drug Discovery and Design Center,Shanghai Institute of Materia Medica,Chinese Academy of Sciences, Shanghai 201203, China.
推荐引用方式
GB/T 7714
Liu Peng,Zhou Yunfei,Zhang Yong,et al. Research progress in VEGFR-2 inhibitors[J]. Acta Pharmaceutica Sinica,2017,52(4):531-540.
APA Liu Peng.,Zhou Yunfei.,Zhang Yong.,Wang Guimin.,Chen Zhaoqiang.,...&Zhu Weiliang.(2017).Research progress in VEGFR-2 inhibitors.Acta Pharmaceutica Sinica,52(4),531-540.
MLA Liu Peng,et al."Research progress in VEGFR-2 inhibitors".Acta Pharmaceutica Sinica 52.4(2017):531-540.

入库方式: OAI收割

来源:上海药物研究所

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