EGFR-IN-1 HCl is an orally bioavailable and irreversible L858R/T790M mutant specific EGFR inhibitor. EGFR-IN-1 HCl highly potently inhibits Gefitinib-resistant EGFR L858R, T790M with 100-fold selectivity over wild-type EGFR. EGFR-IN-1 HCl displays strong antiproliferative activity against the H1975 cells and the first line mutant HCC827 cells. Antitumor activity. References: [1]. Wurz RP, et al. Oxopyrido[2,3-d]pyrimidines as Covalent L858R/T790M Mutant Selective Epidermal Growth Factor Receptor (EGFR) Inhibitors. ACS Med Chem Lett. 2015 Jul 27;6(9):987-92.

纯度：≥98%

CAS：2227455-78-7