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ChemicalBook--->CAS DataBase List--->269390-69-4

269390-69-4

269390-69-4 Structure

269390-69-4 Structure
IdentificationBack Directory
[Name]

N-(4-CHLOROPHENYL)-2-[(PYRIDIN-4-YLMETHYL)AMINO]BENZAMIDE
[CAS]

269390-69-4
[Synonyms]

Valatinib
VEGFR-IN-1
VEGFR IN 1,VEGFRIN1
VEGFR Tyrosine Kinase
VEGFR Tyrosine Kinase Inhibitor II
VEGF RECEPTOR TYROSINE KINASE INHIBITOR II
N-(4-CHLOROPHENYL)-2-[(PYRIDIN-4-YLMETHYL)AMINO]BENZAMIDE
Benzamide, N-(4-chlorophenyl)-2-[(4-pyridinylmethyl)amino]-
[Molecular Formula]

C19H16ClN3O
[MDL Number]

MFCD09037563
[MOL File]

269390-69-4.mol
[Molecular Weight]

337.8
Chemical PropertiesBack Directory
[Boiling point ]

463.6±40.0 °C(Predicted)
[density ]

1.331±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMF: 50 mg/ml; DMSO: 50 mg/ml; DMSO:PBS(pH 7.2) (1:3): 0.25 mg/ml; Ethanol: 25 mg/ml
[form ]

A crystalline solid
[pka]

12.62±0.70(Predicted)
[color ]

White to off-white
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280-P301+P312-P302+P352-P305+P351+P338
Hazard InformationBack Directory
[Uses]

VEGFR Tyrosine Kinase Inhibitor II is an agent that potently inhibits kinase activities of KDR, Flt-1 and c-Kit.
[Biological Activity]

Cell permeable: yes''Primary Target
Kinase activities of KDRFlt-1 and c-Kit''Product competes with ATP.''Reversible: yes''Target IC50: 20 nM180 nM and 240 nM against kinase activities of KDRFlt-1 and c-Kitrespectively
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