Synthesis and antitumor evaluation of novel 5-substituted-4-hydroxy-8-nitroquinazolines as EGFR signaling-targeted inhibitors-Reference-Cited by-同舟云学术

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Synthesis and antitumor evaluation of novel 5-substituted-4-hydroxy-8-nitroquinazolines as EGFR signaling-targeted inhibitors

Published:2005-10 Issue:19 Volume:13 Page:5613-5622
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Jin Yi,Li Hui-Yuan,Lin Li-Ping,Tan Jinzhi,Ding Jian,Luo Xiaomin,Long Ya-Qiu

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference21 articles.

1. Untangling the ErbB signalling network

2. ErbB-2, the preferred heterodimerization partner of all ErbB receptors, is a mediator of lateral signaling

3. Tyrosine kinases as targets in cancer therapy – successes and failures

4. Epidermal growth factor receptor tyrosine kinase inhibitors

5. Protein tyrosine kinase inhibitors as anticancer agents

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2. Reactivity of 2,2‐disubstituted quinazolinone towards electrophilic substitution: First in silico design to verify experimental evidence of quinazolinone‐based new organic compounds;Journal of Physical Organic Chemistry;2023-02-03

3. Synthesis, Anticancer and Antiviral Activity Studies of 1,3,4-Oxadiazoles: A Review;Asian Journal of Chemistry;2022

4. 3,4-Dihydroquinazolin-8-yl-3-phenylurea Derivatives: Synthesis, VEGFR-2 Kinase Inhibiting Activity, and Molecular Docking;Russian Journal of General Chemistry;2021-09

5. Discovery of arylamide-5-anilinoquinazoline-8-nitro derivatives as VEGFR-2 kinase inhibitors: Synthesis, in vitro biological evaluation and molecular docking;Bioorganic & Medicinal Chemistry Letters;2019-12

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