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UHRF1 PHD inhibitor MLD4

Chemical Structure : UHRF1 PHD inhibitor MLD4

CAS No.: 922067-76-3

UHRF1 PHD inhibitor MLD4

Catalog No.: PC-72377Not For Human Use, Lab Use Only.

UHRF1 PHD inhibitor MLD4 is a specific compound that selectively inhibits the UHRF1-histone interaction (IC50=12.4 uM), targets the PHD finger of UHRF1, specifically disrupting histone H3 arginine 2 interactions with the PHD finger.

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    Biological Activity

    UHRF1 PHD inhibitor MLD4 is a specific compound that selectively inhibits the UHRF1-histone interaction (IC50=12.4 uM), targets the PHD finger of UHRF1, specifically disrupting histone H3 arginine 2 interactions with the PHD finger.
    UHRF1 PHD inhibitor MLD4 inhibited binding between H3K9me3(FAM) and UHRF1 with IC50 of 24-26 uM, displace UHRF1-histone H3 binding in cells.

    Physicochemical Properties

    M.Wt 416.522
    Formula C22H32N4O4
    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

    N1-(2-(1-methylindolin-5-yl)-2-morpholinoethyl)-N2-((tetrahydrofuran-2-yl)methyl)oxalamide

    References

    1. Wallace H Liu, et al. Biochemistry. 2022 Feb 10.

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