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Vandetanib

Chemical Structure : Vandetanib

CAS No.: 443913-73-3

Vandetanib (ZD6474;ZD-6474;ZD 6474)

Catalog No.: PC-42496Not For Human Use, Lab Use Only.

Vandetanib (ZD6474) is a potent and selective VEGFR2 (KDR) inhibitor with IC50 of 40 nM.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

Vandetanib (ZD6474) is a potent and selective VEGFR2 (KDR) inhibitor with IC50 of 40 nM.
Vandetanib (ZD6474) shows weak inhibition for VEGFR3 and EGFR (IC50 is 100 nM and 500 nM respectively).
Vandetanib (ZD6474) displays excellent selectivity over erbB2, MEK, CDK-2, Tie-2, IGFR-1R, PDK, PDGFRβ, and Akt (IC50=1.1-100 uM).
Vandetanib (ZD6474) has excellent solubility and good oral bioavailability.

Physicochemical Properties

M.Wt 475.354
Formula C22H24BrFN4O2
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
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Solubility

DMSO: 27.5 mg/mL

Chemical Name/SMILES

4-Quinazolinamine, N-(4-bromo-2-fluorophenyl)-6-methoxy-7-[(1-methyl-4-piperidinyl)methoxy]-

References

1. Hennequin LF, et al. J Med Chem. 2002 Mar 14;45(6):1300-12.

2. Wedge SR, et al. Cancer Res. 2002 Aug 15;62(16):4645-55.

3. Carlomagno F, et al. Cancer Res. 2002 Dec 15;62(24):7284-90.

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