EP26 is a potent and orally active EGFR and PD-L1 inhibitor with IC50 values of 48.6 nM, 1.77 µM, respectively. EP26 decreased the protein expression of p-EGFR. EP26 induces cell cycle arrest at G0/G1 phase. EP26 has the potential for the research of glioblastoma[1].
Molecular Weight:
737.26
Formula:
C42H42ClFN4O5
Target:
EGFR,PD-1/PD-L1
Application Notes:
MCE Product type: Reference compound1
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