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USP10 inhibitor D1

Chemical Structure : USP10 inhibitor D1

CAS No.: 3059565-11-3

USP10 inhibitor D1

Catalog No.: PC-22313Not For Human Use, Lab Use Only.

USP10 inhibitor D1 is a potent, selective small molecule ubiquitin-specific protease 10 (USP10) inhibitor with IC50 of 7.2 uM, KD of 5.24 uM in microscale thermophoresis (MST)-based binding assay.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

    Biological Activity

    USP10 inhibitor D1 is a potent, selective small molecule ubiquitin-specific protease 10 (USP10) inhibitor with IC50 of 7.2 uM, KD of 5.24 uM in microscale thermophoresis (MST)-based binding assay.
    USP10 inhibitor D1 does not inhibit the deubiquitinase activity of USP7 at 10 uM.
    USP10 inhibitor D1 inhibits the proliferation of hepatocellular carcinoma cell (Huh-7, IC50=2.3 uM) by inducing cell apoptosis and S-phase arrest.
    USP10 inhibitor D1 inducing the degradation of USP10-related substrate protein by inhibiting USP10.

    Physicochemical Properties

    M.Wt 512.99
    Formula C29H25ClN4O3
    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

    N-(4-chlorophenethyl)-2-(7-methyl-4-oxo-3-(3-(o-tolyl)-1,2,4-oxadiazol-5-yl)quinolin-1(4H)-yl)acetamide

    References

    1. Yang Lu, et al. Eur J Med Chem. 2024 May 5:272:116468.

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