ChemicalBook--->CAS DataBase List--->694522-87-7

694522-87-7

694522-87-7 Structure

694522-87-7 Structure
IdentificationBack Directory
[Name]

GO 289)
[CAS]

694522-87-7
[Synonyms]

GO 289)
(EZ)-GO289
GO289 (GO-289
5-Bromo-2-methoxy-4-(((3-(methylthio)-5-phenyl-4H-1,2,4-triazol-4-yl)imino)methyl)phenol
Phenol, 5-bromo-2-methoxy-4-[[[3-(methylthio)-5-phenyl-4H-1,2,4-triazol-4-yl]imino]methyl]-
Inhibitor,cancer,(E/Z)GO289,circadian,(E/Z)-GO-289,cell,clock,rhythms,growth,(E/Z) GO289,phosphorylation,(E/Z)-GO289,Casein Kinase,inhibit
[Molecular Formula]

C17H15BrN4O2S
[MDL Number]

MFCD03718152
[MOL File]

694522-87-7.mol
[Molecular Weight]

419.3
Chemical PropertiesBack Directory
[Boiling point ]

618.0±65.0 °C(Predicted)
[density ]

1.52±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO: 2mg/mL, clear
[form ]

Solid
[pka]

7.53±0.40(Predicted)
[color ]

White to off-white
Safety DataBack Directory
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

GO289, is a new potent and highly selective CK2 inhibitor, which strongly lengthens circadian period. It inhibits multiple phsphorylation sites on clock proteins, including PER2 S693. GO289, also exhibited cell type-dependent inhibition of cancer cell growth that correlated with cellular clock function.
[Biological Activity]

GO289 is a highly potent and selective casein kinase CK2 (CKII) inhibitor (IC50 = 7 nM/CK213 μM/PIM2>50 μM/CLK2; <50% inhibition of CK1α/δ/γ and 56 other kinases at 5 μM) th at targets CK2-specific residues (CK2α V66M163and H160) with more overall interactions at the CK2 ATP-binding pocket than TBBDM at & CX-4945. GO289 selectively inhibits cellular CK1 substrates phosphorylation (0.8-8 μM; HEK293TU2OS)including clock proteins PER2CRY1CLOCK & BMAL1and displays circadian period-lengthening (Bmal1-dLuc USOS EC50 = 3.3 μM) as well as growth inhibitory potency in CK2-dependent human renal cell carcinoma (RCC) cultures.
Spectrum DetailBack Directory
[Spectrum Detail]

GO 289)(694522-87-7)1HNMR
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