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Nintedanib
Cat. No.:
0225LY-1106
Appearance:
Solid
Purity:
≥99%
Identity:
Confirmed by NMR.
Size:
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Product Overview
Description:
Nintedanib operates as a triple vascular kinase inhibitor that suppresses the VEGFR, FGFR, and PDGFR families (with various IC50s ranging from 10 nM to 108 nM) to exert antitumor effects by blocking angiogenesis.
Synonym:
BIBF 1120; Intedanib; 656247-17-5; Vargatef; Intedanib; BIBF-1120; Nintedanib (BIBF 1120); (Z)-methyl 3-((4-(N-methyl-2-(4-methylpiperazin-1-yl)acetamido)phenylamino)(phenyl)methylene)-2-oxoindoline-6-carboxylate; Methyl (3Z)-3-[[4-[methyl-[2-(4-methylpiperazin-1-yl)acetyl]amino]anilino]-phenylmethylidene]-2-oxo-1H-indole-6-carboxylate; 1H-Indole-6-carboxylic acid, 2,3-dihydro-3-[[[4-[methyl[2-(4-methyl-1-piperazinyl)acetyl]amino]phenyl]amino]phenylmethylene]-2-oxo-, methyl ester; methyl 2-hydroxy-3-[N-[4-[methyl-[2-(4-methylpiperazin-1-yl)acetyl]amino]phenyl]-C-phenylcarbonimidoyl]-1H-indole-6-carboxylate; (Z)-Methyl 3-(((4-(N-methyl-2-(4-methylpiperazin-1-yl)acetamido)phenyl)amino)(phenyl)methylene)-2-oxoindoline-6-carboxylate; (Z)-Methyl 3-((4-(N-methyl-2-(4-methylpiperazin-1-yl)acetamido)-phenylamino)(phenyl)methylene)-2-oxoindoline-6-carboxylate; Methyl (3Z)-3-(((4-(N-methyl-2-(4-methylpiperazin-1-yl)acetamido)phenyl)amino)(phenyl)methylidene)-2-oxo-2,3-dihydro-1h-indole-6-carboxylate; Methyl (3Z)-3-[({4-[N-methyl-2-(4-methylpiperazin-1-yl)acetamido]phenyl}amino)(phenyl)methylidene]-2-oxo-2,3-dihydro-1H-indole-6-carboxylate; Methyl (3Z)-3-[(4-{methyl[(4-methylpiperazin-1-yl)acetyl]amino}anilino)(phenyl)methylidene]-2-oxo-2,3-dihydro-1H-indole-6-carboxylate
CAS No.:
656247-17-5
Compound CID:
135423438
Formula:
C31H33N5O4
Formula Weight:
539.62
Specification
Targets&IC50:
PDGFRα: 59 nM (cell free); FGFR1: 69 nM (cell free); FGFR2: 37 nM (cell free); VEGFR1: 34 nM (cell free); VEGFR3: 13 nM (cell free); VEGFR2: 13 nM (cell free)
Relative Density:
1.284 g/cm3
Stability:
3 years in powder form.
Storage:
Storage at -20°C.
Applications:
Nintedanib can be used in pulmonary and oncology studies to evaluate the triple inhibition of VEGFR, PDGFR, and FGFR signaling pathways.
Library Information
Target:
Src; FGFR; FLT3; VEGFR; PDGFR
Receptor:
FGFR1; FGFR2; FGFR3; FLT3; Lck; PDGFRα; PDGFRβ; VEGFR1; VEGFR2; VEGFR3
Pathways:
Angiogenesis; Tyrosine kinase/adaptors
Plate Number:
AOCL-15
Plate Location:
c2
Empty Location:
a1-h1; a12-h12
Container:
96-well plate
Formulation:
10mM DMSO
DMSO Max Solubility:
13.1 mg/mL; 24.28 mM
Water Max Solubility:
<1 mg/mL (insoluble or slightly soluble)
Ethanol Max Solubility:
3 mg/mL; 5.56 mM
ALogP:
2.965
HBA_Count:
4
HBD_Count:
2
Rotatable Bond:
8





