Potent inhibitor of ErbB receptor family tyrosine kinases (IC50
values are 0.008, 49 and 52 nM for EGFR, ErbB2 and ErbB2/ErbB4 respectively) that does not inhibit FGF or PDGF-mediated tyrosine phosphorylation. Induces G1
cell cycle arrest in MCF10A cells and is antiproliferative in A431 human epidermal carcinoma cells.
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Biochemical and antiproliferative properties of 4-[ar(alk)ylmino]pyridopyrimidines, a new chemical class of potent and specific epidermal growth factor receptor tyrosine kinase inhibitor.
Fry et al.
G1 cell cycle arrest due to inhibition of erbB family receptor tyrosine kinases does not require the retinoblastoma protein.
Gonzales et al.
Exp.Cell Res., 2005;303:56
Growth inhibition of nasopharyngeal carcinoma cells by EGF receptor tyrosine kinase inhibitors.
Sun et al.
Anticancer Res., 1999;19:919