ASP8273 is a small molecule, irreversible TKI inhibitor that inhibits the kinase activity of EGFR mutations including T790M, with limited activity against EGFR wild-type NSCLC. In the in vitro enzymatic and cell-based assays, ASP8273 were evaluated against EGFR mutantsand WT EGFR.
MoreEGF816 is a third-generation covalent EGFR inhibitor that has potent inhibitory activity against activating and resistant T790M mutants with low IC50 in various cellular assays.
MoreHM-71224 is an EGFR tyrosine kinase inhibitor.
MoreErlotinib HCl (OSI-744)是一种EGFR抑制剂,IC50为2 nM,对EGFR的选择性比c-Src或v-Abl高1000倍以上。
MoreAfatinib (BIBW2992)是一种不可逆EGFR/HER2抑制剂,对EGFR(wt), EGFR(L858R), EGFR(L858R/T790M)和HER2均有抑制作用,IC50分别为0.5 nM,0.4 nM,10 nM和14 nM;用于Gefitinib抗性的突变型EGFR (L858R-T790M )时,活性增强100倍。
MoreASP8273 is a small molecule, irreversible TKI inhibitor that inhibits the kinase activity of EGFR mutations including T790M, with limited activity against EGFR wild-type NSCLC. In the in vitro enzymatic and cell-based assays, ASP8273 were evaluated against EGFR mutantsand WT EGFR.
MoreEGF816 is a third-generation covalent EGFR inhibitor that has potent inhibitory activity against activating and resistant T790M mutants with low IC50 in various cellular assays.
MoreHM-71224 is an EGFR tyrosine kinase inhibitor.
MoreErlotinib HCl (OSI-744)是一种EGFR抑制剂,IC50为2 nM,对EGFR的选择性比c-Src或v-Abl高1000倍以上。
MoreAfatinib (BIBW2992)是一种不可逆EGFR/HER2抑制剂,对EGFR(wt), EGFR(L858R), EGFR(L858R/T790M)和HER2均有抑制作用,IC50分别为0.5 nM,0.4 nM,10 nM和14 nM;用于Gefitinib抗性的突变型EGFR (L858R-T790M )时,活性增强100倍。
MoreASP8273 is a small molecule, irreversible TKI inhibitor that inhibits the kinase activity of EGFR mutations including T790M, with limited activity against EGFR wild-type NSCLC. In the in vitro enzymatic and cell-based assays, ASP8273 were evaluated against EGFR mutantsand WT EGFR.
MoreEGF816 is a third-generation covalent EGFR inhibitor that has potent inhibitory activity against activating and resistant T790M mutants with low IC50 in various cellular assays.
MoreHM-71224 is an EGFR tyrosine kinase inhibitor.
MoreErlotinib HCl (OSI-744)是一种EGFR抑制剂,IC50为2 nM,对EGFR的选择性比c-Src或v-Abl高1000倍以上。
MoreAfatinib (BIBW2992)是一种不可逆EGFR/HER2抑制剂,对EGFR(wt), EGFR(L858R), EGFR(L858R/T790M)和HER2均有抑制作用,IC50分别为0.5 nM,0.4 nM,10 nM和14 nM;用于Gefitinib抗性的突变型EGFR (L858R-T790M )时,活性增强100倍。
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