4-Methyl erlotinib, is a potent and selective epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor. 4-Methyl erlotinib potently inhibits EGF-mediated tumor cell mitosis by reducing EGFr-specific tyrosine phosphorylation. Using a mouse model of human tumor transplantation, 4-Methyl erlotinib demonstrated significant and sustained suppression of EGFr phosphotyrosine levels, resulting in significant growth inhibition of EGFr-dependent human cancers[1].
Molekulargewicht:
407.46
CAS Nummer:
[1346601-52-2]
Formel:
C23H25N3O4
Target-Kategorie:
EGFR,Mitosis
Anwendungsbeschreibung:
MCE Product type: Reference compound
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