VEGFRK inhibitor
Catalog No. F11-900
| Catalog No. | Pack Size | Price (USD) | |
|---|---|---|---|
| F11-900-10 | 10 mg | $60 | |
| F11-900-50 | 50 mg | $240 | |
| F11-900-BULK | BULK | Contact Us |
Overview:
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 (1). Inhibits colony formation in seven cancer cell lines (2). Displays anti-angiogenesis activity (3).
References:
1. SR Wedge et al. Cancer Res. 2002 62:4645
2. F Ciardiello et al. Clin. Cancer Res. 2003 9:1546
3. RS Herbst et al. Expert Opin. Investig. Drugs 2007 16:239
CAS Registry Number:
443913-73-3
Molecular Formula:
C22H24BrFN4O2
Appearance:
White to off-white powder
Melting Point:
N/A
Molecular Weight:
475.4
Purity:
>98% (TLC); NMR (Conforms)
Solubilization:
May be dissolved in DMSO (30 mg/ml); or ethanol (10 mg/ml, warm)
Aliases:
1. 4-(4-Bromo-2-fluoroanilino)-6-methoxy-7-[(1-methylpiperidin-4-yl) methoxy] quinazoline
2. ZD6474
Storage and Stability:
Store desiccated as supplied at -20oC for up to 2 years. Store solutions at -20oC for up to 1 month.
Molecular Structure:
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There are no related publications available for this product.
Angiogenesis, Cancer, Cell Cycle, Neurobiology
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