A CK2 inhibitor
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Information provided in the product description is from published literature. Due to the nature of scientific experimentation, your results (e.g., selectivity and effective concentrations) or specific application for this product may differ. If you have questions about how this product fits your application, please contact our technical support staff.

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GO289

Item No. 43959

Technical Information
Formal Name
5-bromo-2-methoxy-4-[[[3-(methylthio)-5-phenyl-4H-1,2,4-triazol-4-yl]imino]methyl]-phenol
CAS Number
694522-87-7
Molecular Formula
C17H15BrN4O2S
Formula Weight
Purity
≥98%
A solid
DMSO: Slightly soluble: 0.1-1 mg/ml
SMILES
CSC1=NN=C(C2=CC=CC=C2)N1N=CC3=C(Br)C=C(O)C(OC)=C3
InChi Code
InChI=1S/C17H15BrN4O2S/c1-24-15-8-12(13(18)9-14(15)23)10-19-22-16(20-21-17(22)25-2)11-6-4-3-5-7-11/h3-10,23H,1-2H3
InChi Key
DARDDBZKGVEVKB-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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Certificates of Analysis & Batch Specific Data

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    Product Description

    GO289 is an inhibitor of casein kinase 2 (CK2; IC50 = 7 nM).1 It is selective for CK2 over a panel of 59 other kinases at 5 µM. GO289 (8 or 24 µM) increases the circadian period in a reporter assay using U2OS cells. It decreases levels of phosphorylated Akt and cell division cycle 37 (Cdc37) in C2C12 skeletal muscle myoblasts when used at concentrations of 1, 2, 3, or 4 µM.2

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Oshima, T., Niwa, Y., Kuwata, K., et alCell-based screen identifies a new potent and highly selective CK2 inhibitor for modulation of circadian rhythms and cancer cell growth. Sci. Adv. 5(1), eaau9060 (2019).

    2. Borgo, C., Cesaro, L., Hirota, T., et alComparing the efficacy and selectivity of Ck2 inhibitors. A phosphoproteomics approach. Eur. J. Med. Chem. 214, 113217 (2021).