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• W2012212912 abstract "The receptortyrosine kinase c-Met is an attractive target for therapeutic treatment of cancers nowadays. The discovery of small molecule inhibitors is of special interest in the blockade of the c-Met kinase pathway. Here, we initiated our study from compound 1a, a novel inhibitor against c-Met kinase. A substructure similarity search against the SPECS database and chemical synthesis methods were performed to obtain a series of pyrazolidine-3,5-dione derivatives. Through the enzyme-based assay against c-Met kinase, 4 compounds (1c, 1e, 1m and 1o) showed potential inhibitory activity, with IC50 values mostly less than 10 μM. Based on the structure–activity relationship (SAR) and binding mode analysis, a focused combinatorial library was designed by the LD1.0 program. Taking into account ADMET properties and synthesis accessibility, seven candidate compounds (5a–g) were successfully synthesized. The activity of the most potent compounds 5b (IC50 = 0.46 μM) was 20 fold higher than that of the lead 1a. Taken together, our findings identified the pyrazolidine-3,5-dione derivatives as potent inhibitors against c-Met kinase and demonstrated the efficiency of the strategy in the development of small molecules against c-Met kinase." @default.
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• W2012212912 date "2012-01-01" @default.
• W2012212912 modified "2023-09-24" @default.
• W2012212912 title "Discovering potent inhibitors against c-Met kinase: molecular design, organic synthesis and bioassay" @default.
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• W2012212912 doi "https://doi.org/10.1039/c1ob06186k" @default.
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