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Lucitanib
Cat. No.:
OB0225WX-2254
Appearance:
Solid
Purity:
≥96%
Identity:
Confirmed by NMR, and LC-MS.
Size:
Add to basket
Product Overview
Description:
Lucitanib is a potent multi-kinase inhibitor targeting VEGFR1/2/3 and FGFR1/2 with high affinity, featuring IC50 values ranging from 7 nM to 82.5 nM.
Synonym:
E-3810; 1058137-23-7; E-3810 amine; E-3810 free base; 6-((7-((1-aminocyclopropyl)methoxy)-6-methoxyquinolin-4-yl)oxy)-N-methyl-1-naphthamide; 6-[7-[(1-aminocyclopropyl)methoxy]-6-methoxyquinolin-4-yl]oxy-N-methylnaphthalene-1-carboxamide; CHEBI:65209; 6-({7-[(1-Aminocyclopropyl)methoxy]-6-Methoxyquinolin-4-Yl}oxy)-N-Methylnaphthalene-1-Carboxamide; 1-Naphthalenecarboxamide, 6-((7-((1-aminocyclopropyl)methoxy)-6-methoxy-4-quinolinyl)oxy)-n-methyl-; 6-({7-[(1-aminocyclopropyl)methoxy]-6-methoxyquinolin-4-yl}oxy)-N-methyl-1-naphthamide; 6-((7-((1-Aminocyclopropyl)methoxy)-6-methoxyquinolin-4-yl)oxy)-n-methylnaphthalene-1-carboxamide; 6-(7-((1-aminocyclopropyl)methoxy)-6-methoxy-quinolin-4-yloxy)-N-methyl-1-naphthamide
CAS No.:
1058137-23-7
Compound CID:
25031915
Formula:
C26H25N3O4
Formula Weight:
443.49
Specification
Targets&IC50:
VEGFR1: 7 nM; FGFR2: 82.5 nM; VEGFR2: 25 nM; VEGFR3: 10 nM; FGFR1: 17.5 nM
Relative Density:
1.285 g/cm3
Stability:
3 years in powder form.
Storage:
Storage at -20°C.
Applications:
Lucitanib is utilized in advanced oncology research as a potent multi-kinase inhibitor targeting VEGFR, FGFR, and PDGFR to investigate the disruption of tumor angiogenesis and growth signaling.
Library Information
Target:
FGFR; VEGFR
Receptor:
FGFR1; FGFR2; VEGFR1; VEGFR2; VEGFR3
Pathways:
Tyrosine kinase/adaptors; Angiogenesis
Plate Number:
AOCL-29
Plate Location:
g11
Empty Location:
a1-h1; a12-h12
Container:
96-well plate
Formulation:
10mM DMSO
DMSO Max Solubility:
25 mg/mL; 56.37 mM





