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GPS192

Chemical Structure : GPS192

CAS No.:

GPS192 (GPS 192)

Catalog No.: PC-20474Not For Human Use, Lab Use Only.

GPS192 (GPS 167) is a specific small molecule splicing regulator SRSF10 inhibitor, modulates BCLAF1 splicing with IC50 of 2 uM in human colorectal HCT116 cells, directly inhibits CLK1, CLK2 and CLK4, but not SRPK1 and DYRK1A.

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    Biological Activity

    GPS192 (GPS 167) is a specific small molecule splicing regulator SRSF10 inhibitor, modulates BCLAF1 splicing with IC50 of 2 uM in human colorectal HCT116 cells, directly inhibits CLK1, CLK2 and CLK4, but not SRPK1 and DYRK1A.
    GPS192 promotes the dephoshorylation of SRSF10 and changes its interaction with partner proteins.
    GPS192 treatment leads to a partial dephosphorylation of SRSF10 and increases the recovery of CLK1 and CLK4.
    GPS192 impairs the growth of cancer cell line, elicits p53-dependent cytotoxicity.

    Physicochemical Properties

    M.Wt 392.46
    Formula C18H12N6OS2
    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-((1H-indazol-5-yl)amino)-N-(benzo[d]thiazol-6-yl)thiazole-4-carboxamide

    References

    1. Muhammad Sohail, et al. NAR Cancer. 2021 May 25;3(2):zcab019.

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