ChemicalBook--->CAS DataBase List--->227449-73-2

227449-73-2

227449-73-2 Structure

227449-73-2 Structure
IdentificationBack Directory
[Name]

Syk Inhibitor II
[CAS]

227449-73-2
[Synonyms]

Syk Inhibitor II
Syk Inhibitor II (hydrochloride)
2-[(2-Aminoethyl)amino]-4-[[3-(trifluoromethyl)phenyl]amino]-5-pyrimidinecarboxamide Hydrochloride
[Molecular Formula]

C14H16ClF3N6O
[MOL File]

227449-73-2.mol
[Molecular Weight]

376.77
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

DMF: 2 mg/ml; DMSO: 30 mg/ml; Ethanol: 0.3 mg/ml; PBS (pH 7.2): 10 mg/ml
[form ]

A crystalline solid
[color ]

off-white
[InChI]

1S/C14H15F3N6O.2ClH.2H2O/c15-14(16,17)8-2-1-3-9(6-8)22-12-10(11(19)24)7-21-13(23-12)20-5-4-18;;;;/h1-3,6-7H,4-5,18H2,(H2,19,24)(H2,20,21,22,23);2*1H;2*1H2
[InChIKey]

LCACSMNPIITJGG-UHFFFAOYSA-N
Safety DataBack Directory
[WGK Germany ]

WGK 1
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

2-[(2-Aminoethyl)amino]-4-[[3-(trifluoromethyl)phenyl]amino]-5-pyrimidinecarboxamide Hydrochloride was identified via a small molecule screening assay. In addition, this compound inhibits tyrosine kinase and may be a useful reagent to investigate cellular signalling pathways.
[Biological Activity]

Cell permeable: yes''Primary Target
Syk''Product competes with ATP.''Reversible: yes''Target IC50: 41 nM against Syk; 460 nM against FcεRI-mediated 5-HT release in RBL-2H3 cells in vitro
[in vivo]

Syk Inhibitor II (Compound 9a; 10-100 mg/kg) dihydrochloride is subcutaneously administered to mice 30 min before antigen challenge. Syk Inhibitor II inhibits the anaphylaxis reaction dose-dependently with an ID50 value of 13.2 mg/kg[1].

Animal Model:ICR mice[1]
Dosage:10, 30, 100 mg/kg
Administration:S.c.; 30 min before antigen challenge
Result:Inhibited the anaphylaxis reaction dose-dependently with an ID50 value of 13.2 mg/kg.
[IC 50]

5-HT Receptor: 460 nM (IC50)
[storage]

Store at -20°C
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