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Research progress on anti-tumor drug resistance of pyridazine-containing structural compounds
Yu-Lin Liu1, Bing-Qian Li1, Lin-Lin Zhang1
1State Key Laboratory of Esophageal Cancer Prevention and Treatment, Key Laboratory of Advanced Pharmaceutical Technology, Ministry of Education of China, School of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou 450001, China.
Abstract:
Pyridazine is an aromatic heterocyclic organic compound with a six-membered ring containing four carbon and two nitrogen atoms. Studies have demonstrated their multiple pharmacological properties, including anticancer, antiviral, and anti-Parkinson's disease effects. Recently, there has been increasing interest in their potential anti-tumor resistance activity. Several pyridazine-based drugs and their analogs are currently undergoing clinical trials at different stages, suggesting that pyridazine is a promising chemical structure for drug development. Notably, modifications of pyridazine structures significantly affect their anti-tumor resistance activity. This review summarizes current advances in developing pyridazine derivatives as anti-tumor drug, highlighting key SAR-based design optimization strategies, molecular design principles, and mechanistic insights into target binding. These insights could pave the way for the development of more effective anti-tumor agents overcoming resistance.
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