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SGC-STK17B-1

Chemical Structure : SGC-STK17B-1

CAS No.: 2650530-00-8

SGC-STK17B-1

Catalog No.: PC-38222Not For Human Use, Lab Use Only.

SGC-STK17B-1 is a potent, selective, ATP-competitive inhibitor of death-associated protein kinase family member STK17B (DRAK2) with IC50 of 34 nM, >100-fold selectivity over STK17A.

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    Biological Activity

    SGC-STK17B-1 is a potent, selective, ATP-competitive inhibitor of death-associated protein kinase family member STK17B (DRAK2) with IC50 of 34 nM, >100-fold selectivity over STK17A.
    SGC-STK17B-1 is also >100-fold selective over all of the other kinases tested, with only STK17A, CAMKK1, and AURKB (IC50s=5-9 uM) in panel of 403 wild type human kinase assays.
    SGC-STK17B-1 demonstrated the highest cell potency in the NanoBRET target engagement assay (IC50=190 nM).
    SGC-STK17B-1 is the first truly potent and selective chemical probe of STK17B.

    Physicochemical Properties

    M.Wt 358.448
    Formula C16H10N2O2S3
    Appearance Solid
    CAS No.
    Storage
    Solide Powder
    -20°C 12 Months; 4°C 6 Months
    In Solvent
    -80°C 6 Months; -20°C 6 Months
    Shipping
    Solubility

    10 mM in DMSO

    Chemical Name/SMILES

    2-((6-(Benzo[b]thiophen-2-yl)thieno[3,2-d]pyrimidin-4-yl)thio)acetic acid

    References

    1. Alfredo Picado, et al. J Med Chem. 2020 Dec 10;63(23):14626-14646.

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