Mutated EGFR-IN-2 is a compound that blocks the activity of the epidermal growth factor receptor (EGFR) and human epidermal growth factor receptor 2 (HER2), both of which are involved in driving the growth and proliferation of certain types of cancer cells. It targets EGFR (ex19del/T790M), EGFR (L858R/T790M), EGFR(L858R), and EGFRex19del.
Mutated EGFR-IN-2 can be used to study its effect as a selective inhibitor of mutant EGFR in cancer treatment.
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