ChemicalBook--->CAS DataBase List--->2378855-09-3

2378855-09-3

2378855-09-3 Structure

2378855-09-3 Structure
IdentificationBack Directory
[Name]

INDEX NAME NOT YET ASSIGNED
[CAS]

2378855-09-3
[Synonyms]

VRK-IN-1
[Molecular Formula]

C18H11F4NO2
[MDL Number]

MFCD34368509
[MOL File]

2378855-09-3.mol
[Molecular Weight]

349.28
Chemical PropertiesBack Directory
[Boiling point ]

400.2±40.0 °C(Predicted)
[density ]

1.436±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO : 100 mg/mL (286.30 mM; Need ultrasonic)
[form ]

Solid
[pka]

5.78±0.25(Predicted)
[color ]

White to off-white
[SMILES]

FC1=CC(C2=CN=C(C)C(C3=CC(F)=C(O)C(F)=C3)=C2)=CC(F)=C1O
Hazard InformationBack Directory
[Uses]

VRK-IN-1 is a potent and selective inhibitor of vaccinia-related kinases 1 (VRK1), with an IC50 of 150 nM. VRK1 is human Ser/Thr protein kinases associated with increased cell division and neurological disorders[1].
[Biological Activity]

VRK-IN-1 is a potent and selective inhibitor of vaccinia-related kinases 1 (VRK1), with an IC50 of 150 nM. VRK1 is human Ser/Thr protein kinases associated with increased cell division and neurological disorders[1]. VRK-IN-1 binds to VRK1-FL by enthalpy-driven, with a Kd of 190 nM[1].VRK-IN-1 (0.4-25 μM; 24 h) slightly decreases the viability of human HeLa cells at the concentration of 3.2 μM[1].
[References]

[1]. Serafim RAM, et, al. Development of Pyridine-based Inhibitors for the Human Vaccinia-related Kinases 1 and 2. ACS Med Chem Lett. 2019 Aug 19;10(9):1266-1271.
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