Design, synthesis and biological evaluation of structurally new 4-indolyl quinazoline derivatives as highly potent, selective and orally bioavailable EGFR inhibitors-Reference-Cited by-同舟云学术

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Design, synthesis and biological evaluation of structurally new 4-indolyl quinazoline derivatives as highly potent, selective and orally bioavailable EGFR inhibitors

Published:2024-01 Issue: Volume:142 Page:106970
ISSN:0045-2068
Container-title:Bioorganic Chemistry
language:en
Short-container-title:Bioorganic Chemistry

Author:

He Pengxing^ORCID,Du Linna,Dai Qingqing,Li Guobo,Yu Bin,Chang Linlin

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Molecular Biology,Biochemistry

Reference62 articles.

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3. Mutation incidence and coincidence in non small-cell lung cancer: meta-analyses by ethnicity and histology (mutMap);Dearden;Ann. Oncol.,2013

4. ctDNA Determination of EGFR Mutation Status in European and Japanese Patients with Advanced NSCLC: The ASSESS Study;Reck;J. Thorac. Oncol.,2016

5. BB, a new EGFR inhibitor, exhibits prominent anti-angiogenesis and antitumor activities;Sun;Cancer Biol. Ther.,2009

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1. A concise review on recent development of indole derivatives for anticancer activities;Journal of the Indian Chemical Society;2024-10

2. Indole Compounds in Oncology: Therapeutic Potential and Mechanistic Insights;Pharmaceuticals;2024-07-10

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