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1. C5-substituted pyrido[2, 3-d]pyrimidin-7-ones as highly specific kinase inhibitors targeting the clinical resistance-related EGFRT790M mutant1. Issue 9 (2nd September 2015)

10. Pyrimido[4, 5‐d]pyrimidin‐4(1H)‐one Derivatives as Selective Inhibitors of EGFR Threonine790 to Methionine790 (T790M) Mutants1. (26th June 2013)