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• W2780454526 abstract "To address drug resistance caused by ALK kinase mutations, especially the most refractory and predominant mutation G1202R for the second-generation ALK inhibitor, a series of new diarylaminopyrimidine analogues were designed by incorporating a resorcinol moiety (A-ring) to interact the ALK kinase domain where the G1202R is located. Compound 12d turns out as the most potent with IC50 values of 1.7, 3.5, and 1.8 nM against ALK wild type, gatekeeper mutant L1196M, and the G1202R mutant, respectively. More importantly, compound 12d has excellent inhibitory effects against the proliferation of BaF3 cells specifically expressing ALK wild type, gatekeeper L1196M, and the most challenging mutant G1202R, with IC50 values all less than 1.5 nM. Collectively, compound 12d is worthy of further investigation as a new more potent third-generation ALK inhibitor to circumvent drug resistance of both the first-generation and the second-generation inhibitors." @default.
• W2780454526 created "2018-01-05" @default.
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• W2780454526 date "2018-01-01" @default.
• W2780454526 modified "2023-10-16" @default.
• W2780454526 title "Discovery of 2,4-diarylaminopyrimidines bearing a resorcinol motif as novel ALK inhibitors to overcome the G1202R resistant mutation" @default.
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• W2780454526 doi "https://doi.org/10.1016/j.ejmech.2017.12.060" @default.
• W2780454526 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/29288940" @default.
• W2780454526 hasPublicationYear "2018" @default.
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