Design, Synthesis and Biological Evaluation of Quinoxalin-2(1H)-one Derivatives as EGFR Tyrosine Kinase Inhibitors-Reference-Cited by-同舟云学术

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Design, Synthesis and Biological Evaluation of Quinoxalin-2(1H)-one Derivatives as EGFR Tyrosine Kinase Inhibitors

Published:2015-01-16 Issue:2 Volume:15 Page:267-273
ISSN:1871-5206
Container-title:Anti-Cancer Agents in Medicinal Chemistry
language:en
Short-container-title:ACAMC

Author:

Qin Xuemei,Han Xiao,Hu Liming,Li Zhipeng,Geng Zhufeng,Wang Zhanyang,Zeng Chengchu,Xiao Xiangqian

Publisher

Bentham Science Publishers Ltd.

Subject

Cancer Research,Pharmacology,Molecular Medicine

Cited by 8 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Discovery of Potent Indolyl-Hydrazones as Kinase Inhibitors for Breast Cancer: Synthesis, X-ray Single-Crystal Analysis, and In Vitro and In Vivo Anti-Cancer Activity Evaluation;Pharmaceuticals;2023-12-13

2. Synthesis and Biological Activity of 3,9-Diazatetraasteranes as Novel EGFR Tyrosine Kinase Inhibitors;Russian Journal of General Chemistry;2022-03

3. Dual Targeting of Janus Kinase and Bruton’s Tyrosine Kinase: A New Approach to Control the Pathogenesis of Rheumatoid Arthritis;Pakistan Journal of Zoology;2020

4. Pharmacophore modeling, 3D-QSAR, docking and ADME prediction of quinazoline based EGFR inhibitors;Arabian Journal of Chemistry;2019-12

5. An insight into medicinal chemistry of anticancer quinoxalines;Bioorganic & Medicinal Chemistry;2019-01

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