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ChemicalBook--->CAS DataBase List--->2248003-60-1

2248003-60-1

2248003-60-1 Structure

2248003-60-1 Structure
IdentificationBack Directory
[Name]

AZD3229
[CAS]

2248003-60-1
[Synonyms]

AZD3229
AZD3229 (AZD-3229
AZD3229;AZD 3229;AZD-3229
[Molecular Formula]

C24H26FN7O3
[MOL File]

2248003-60-1.mol
[Molecular Weight]

479.51
Chemical PropertiesBack Directory
[density ]

1.35±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO:68.67(Max Conc. mg/mL);143.21(Max Conc. mM)
DMF:10.0(Max Conc. mg/mL);20.85(Max Conc. mM)
Ethanol:0.3(Max Conc. mg/mL);0.63(Max Conc. mM)
[form ]

A crystalline solid
[pka]

12.75±0.70(Predicted)
[color ]

White to off-white
Spectrum DetailBack Directory
[Spectrum Detail]

AZD3229(2248003-60-1)1HNMR
Hazard InformationBack Directory
[Biological Activity]

AZD3229 is a potent pan-Kit (c-Kit) mutant inhibitor with GI50 of 1-50 nM in a Kit (c-Kit) mutant-driven Ba/F3 cell line. It also inhibits PDGFR mutants (Tel-PDGFRα, Tel-PDGFRβ, V561D/D842V).
[in vivo]

AZD3229 has high bioavailability, low clearance and small volume of distribution in preclinical animal models of mice, rats and dogs. In an in vivo model constructed using the Ba/F3 cell line, AZD3229 at 20 mg/kg bid induces regression of tumor volume more effectively than regorafenib and imatinib at 100 mg/kg qd.

[target]

TargetValue
Kit
()
PDGFRα
()
PDGFRβ
()
[storage]

Store at -20°C
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