Affiliation:
1. School of Pharmaceutical Sciences, Guizhou University, Guiyang 550025, China
2. Guizhou Engineering Laboratory for Synthetic Drugs, Guizhou University, Guiyang 550025, China
Abstract
A series of 1,4-naphthoquinone derivatives containing were synthesized as anti-cancer agents and the crystal structure of compound 5a was confirmed by X-ray diffraction. In addition, the inhibitory activities against four cancer cell lines (HepG2, A549, K562, and PC-3) were tested, respectively, and compound 5i showed significant cytotoxicity on the A549 cell line with the IC50 of 6.15 μM. Surprisingly, in the following preliminary biological experiments, we found that compound 5i induced autophagy by promoting the recycling of EGFR and signal transduction in the A549 cell, resulting in the activation of the EGFR signal pathway. The potential binding pattern between compound 5i and EGFR tyrosine kinase (PDB ID: 1M17) was also identified by molecular docking. Our research paves the way for further studies and the development of novel and powerful anti-cancer drugs.
Funder
National Natural Science Foundation of China
Science and Technology Foundation of Guizhou Province
Guizhou Provincial Young Science and Technology Talents Development Project
Top Science and Technology Talent Program of Guizhou Education Department
Guizhou Provincial Department of Education
Guizhou University Cultivation Project
Guizhou University Talent Introduction Project
Subject
Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science
Cited by
3 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