Chemical Name: 4-(4-Bromo-2-fluoroanilino)-6-methoxy-7-(1-methylpiperidin-4-yl)methoxy]quinazoline. Alternate Names: ZD6474
VEGFRK inhibitor
Molekulargewicht:
475.35
Reinheit:
98% by TLC, NMR (Conforms)
Formulierung:
White or off-white solid
CAS Nummer:
[443913-73-3]
Formel:
C22H24BrFN4O2
Anwendungsbeschreibung:
A potent and selective inhibitor of VEGFR2, (KDR IC50 = 40 nM). Also inhibits fms-like tyrosine kinase 4 (VEGFR3, IC50 = 110 nM) and epidermal growth factor receptor (EGFR/HER1, IC50 = 500 nM) but shows selectivity against a panel of other tyrosine and serine-threonine kinases. Inhibits colony formation in seven cancer cell lines2. Displays anti-angiogenesis activity3.
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