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Vandetanib (ZD6474)

Cat. No.: OB0225WX-2812
Appearance: Solid
Purity: ≥99%
Identity: Confirmed by NMR, and HPLC.
Size:
Vandetanib (ZD6474)
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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
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