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Vandetanib (ZD6474)
Cat. No.:
OB0225WX-2812
Appearance:
Solid
Purity:
≥99%
Identity:
Confirmed by NMR, and HPLC.
Size:
Add to basket
Product Overview
Description:
Vandetanib is a potent multi-kinase inhibitor that targets VEGFR2 (IC50: 40 nM), VEGFR3 (IC50: 110 nM), and EGFR (IC50: 500 nM) and is known to induce autophagy via ROS elevation.
Synonym:
ZD6474; 443913-73-3; Vandetanib; Zactima; Caprelsa; N-(4-Bromo-2-fluorophenyl)-6-methoxy-7-((1-methylpiperidin-4-yl)methoxy)quinazolin-4-amine; N-(4-bromo-2-fluorophenyl)-6-methoxy-7-[(1-methylpiperidin-4-yl)methoxy]quinazolin-4-amine; ZD-6474; ZD 6474; GNF-PF-2188; ZD-64; NSC-744325; N-(4-Bromo-2-fluorophenyl)-6-methoxy-7-((1-methyl-4-piperidinyl)methoxy)-4-quinazolinamine; MFCD07772346; N-(4-Bromo-2-fluorophenyl)-6-methoxy-7-[(1-methyl-4-piperidinyl)methoxy]-4-quinazolinamine; 4-(4-bromo-2-fluoroanilino)-6-methoxy-7-(1-methylpiperidin-4-ylmethoxy)quinazoline; 4-Quninazolinamine, N-(4-bromo-2-fluorophenyl)-6-methoxy-7-((1-methyl-4-piperidinyl)methoxy)-
CAS No.:
443913-73-3
Compound CID:
3081361
Formula:
C22H24BrFN4O2
Formula Weight:
475.35
Specification
Stability:
3 years in powder form.
Storage:
Storage at -20°C.
Applications:
Vandetanib is utilized in oncology research as a potent multi-kinase inhibitor targeting VEGFR, EGFR, and RET to investigate the simultaneous suppression of tumor-induced angiogenesis and growth factor signaling.
Library Information
Target:
EGFR; Reactive oxygen species; VEGFR
Receptor:
EGFR; Reactive oxygen species; VEGFR
Pathways:
Protein tyrosine kinase
Plate Number:
L6700-13
Empty Location:
a1-h1; a12-h12
Container:
96-well plate
Formulation:
2mM DMSO
DMSO Max Solubility:
4 mg/mL; 8.41 mM
ALogP:
5.087
HBA_Count:
4
HBD_Count:
1
Rotatable Bond:
6





