Potent and selective inhibitor of EGFR (IC50 = 3nM). Reduces EGF-stimulated DNA synthesis in Rat-1 fibroblasts by ~75% at 0.25µM. Blocks EGF-dependent src-family kinase activation and p21/Cip 1/WAF1 induction in A431 cells. Also inhibits H2O2-induced sti
Molekulargewicht:
315.8
Reinheit:
98% (HPLC)
CAS Nummer:
[153436-53-4]
Formel:
C16H14ClN3O2
Target-Kategorie:
EGFR
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