PD 174265 is a highly selective, reversible EGFR/ErbB2 tyrosine kinase inhibitor (IC50 = 0.45 nM) and cell differentiation inducer. By blocking receptor autophosphorylation and the downstream ERK signaling pathway (with an IC50 of 0.45 µM for full-length ERK), PD 174265 effectively inhibits tumor growth and exhibits antitumor activity without obvious toxicity in in vivo models. PD 174265 drives oligodendrocyte precursor cells to switch from a proliferative state to a differentiated state, significantly upregulates the expression of myelin proteins such as CNP, PLP and MBP, and induces neurite branching. PD 174265 shows no inhibitory effect on other kinases including insulin, PDGF and basic FGF receptors, and serves as a crucial tool molecule for investigating the treatment of human epidermoid carcinoma and the mechanism of myelin repair in multiple sclerosis[1][2][3][4].
Molecular Weight:
371.23
Purity:
98.35
CAS Number:
[216163-53-0]
Formula:
C17H15BrN4O
Target:
EGFR,ERK,FGFR,PDGFR
Application Notes:
MCE Product type: Reference compound
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