Design, synthesis, and biological evaluation of 2, 4-dichlorophenoxyacetamide chalcone hybrids as potential c-Met kinase inhibitors
Author:
Funder
Indian Council of Medical Research
Publisher
Springer Science and Business Media LLC
Subject
Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics
Link
https://link.springer.com/content/pdf/10.1007/s00044-022-02986-9.pdf
Reference78 articles.
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2. Gentile A, Trusolino L, Comoglio PM. The Met tyrosine kinase receptor in development and cancer. Cancer Metastasis Rev. 2008;27:85–94. https://doi.org/10.1007/s10555-007-9107-6
3. Kim ES, Salgia R. MET pathway as a therapeutic target. J Thorac Oncol. 2009;4:444–7. https://doi.org/10.1097/JTO.0b013e31819d6f91
4. Zhang Y, Xia M, Jin K, Wang S, Wei H, Fan C, Wu Y, Li X, Li X, Li G, Zeng Z, Xiong W. Function of the c-Met receptor tyrosine kinase in carcinogenesis and associated therapeutic opportunities. Mol Cancer. 2018;17:45 https://doi.org/10.1186/s12943-018-0796-y
5. Ghiso E, Giordano S. Targeting MET: why, where and how. Curr Opin Pharm. 2013;13:511–8. https://doi.org/10.1016/j.coph.2013.05.018
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