Discovery of novel 4-arylamino-quinazoline derivatives as EGFRL858R/T790M inhibitors with the potential to inhibit the non-small cell lung cancers-Reference-Cited by-同舟云学术

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Discovery of novel 4-arylamino-quinazoline derivatives as EGFRL858R/T790M inhibitors with the potential to inhibit the non-small cell lung cancers

Published:2022-10 Issue: Volume:127 Page:105994
ISSN:0045-2068
Container-title:Bioorganic Chemistry
language:en
Short-container-title:Bioorganic Chemistry

Author:

Gan Wenhui,Wang Caolin,Pan Qingshan,Li Yuzhen,Guo Yuping,Fan Dang,Peng Yuting,Rao Zixuan,Xu Shan,Zheng Pengwu,Zhu Wufu

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Molecular Biology,Biochemistry

Reference36 articles.

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3. Design and synthesis of 4,6-substituted-(diaphenylamino)quinazolines as potent EGFR inhibitors with antitumor activity;Li;Bioorg. Med. Chem.,2012

4. Non–small cell lung cancer: epidemiology, screening, diagnosis, and treatment, in;Duma;Mayo Clinic Proceedings, Elsevier,2019

5. Identification of EGFR kinase domain mutations among lung cancer patients in China: implication for targeted cancer therapy;Qin;Cell Res.,2005

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2. Design, synthesis, and antiproliferative activities of novel substitutedhydrazone/triazolo-linked quinazoline derivatives;Journal of Molecular Structure;2024-06

3. Recent Advances in Structural Optimization of Quinazoline-Based Protein Kinase Inhibitors for Cancer Therapy (2021–Present);Molecules;2024-02-16

4. Designing strategies, structural activity relationship and biological activity of recently developed nitrogen containing heterocyclic compounds as epidermal growth factor receptor tyrosinase inhibitors;Journal of Molecular Structure;2023-11

5. Nitrogen‐Containing Heterocyclic Scaffolds as EGFR Inhibitors: Design Approaches, Molecular Docking, and Structure‐Activity Relationships;ChemistrySelect;2023-07-10

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