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ChemicalBook--->CAS DataBase List--->915720-21-7

915720-21-7

915720-21-7 Structure

915720-21-7 Structure
IdentificationBack Directory
[Name]

AZ-23
[CAS]

915720-21-7
[Synonyms]

AZ-23
AZ23; AZ-23
5-Chloro-N-[(1S)-1-(5-fluoropyridin-2-yl)ethyl]-N'-(5-isopropoxy-1H-pyrazol-3-yl)pyrimidine-2,4-diamine
(S)-5-chloro-N2-(1-(5-fluoropyridin-2-yl)ethyl)-N4-(5-isopropoxy-1H-pyrazol-3-yl)pyrimidine-2,4-diamine
2,4-Pyrimidinediamine, 5-chloro-N2-[(1S)-1-(5-fluoro-2-pyridinyl)ethyl]-N4-[5-(1-methylethoxy)-1H-pyrazol-3-yl]-
[Molecular Formula]

C17H19ClFN7O
[MDL Number]

MFCD17215208
[MOL File]

915720-21-7.mol
[Molecular Weight]

391.83
Chemical PropertiesBack Directory
[Boiling point ]

596.1±60.0 °C(Predicted)
[density ]

1.411
[storage temp. ]

Store at -20°C
[solubility ]

DMSO:125.0(Max Conc. mg/mL);319.02(Max Conc. mM)
[form ]

Solid
[pka]

12.37±0.10(Predicted)
[color ]

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


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Uses]

5-Chloro-N-[(1S)-1-(5-fluoropyridin-2-yl)ethyl]-N'-(5-isopropoxy-1H-pyrazol-3-yl)pyrimidine-2,4-diamine (AZ-23) is a potent and selective tyrosine kinase inhibitor which may be used in the therapeutic treatment of cancers.
[Biological Activity]

AZ-23 is an ATP-competitive, orally active Trk kinase A/B/C inhibitor with IC50 values of 2 nM (TrkA), 8 nM (TrkB), 24 nM (FGFR1), 52 nM (Flt3) , 55 nM (Ret), 84 nM (MuSk), 99 nM (Lck).
[in vitro]

AZ-23 potently and selectivity inhibits Trk phosphorylation in cells. AZ-23 potently inhibits Trk-mediated survival (EC 50 of 2 nM). AZ-23 Inhibits Trk-Dependent Survival in MCF10ATrkA-Δ and TF-1 Cell Lines.

[in vivo]

AZ-23 shows in vivo TrkA kinase inhibition and efficacy in mice following oral administration in a TrkA-driven allograft model and significant tumor growth inhibition in a Trk-expressing xenograft model of neuroblastoma .

[target]

TrkA

2 nM (IC 50 )

TrkB

8 nM (IC 50 )

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