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KU-177

Chemical Structure : KU-177

CAS No.: 1160952-43-1

KU-177 (KU177)

Catalog No.: PC-72658Not For Human Use, Lab Use Only.

KU-177 (KU-177) is a selective small molecule inhibitor of Hsp90 cochaperone AHSA1 (Aha1 ,activator of Hsp90 ATPase homolog 1, Activator of HSP90 ATPase Activity 1), inhibits interaction between Hsp90 and Aha1.

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

    Biological Activity

    KU-177 (KU-177) is a selective small molecule inhibitor of Hsp90 cochaperone AHSA1 (Aha1 ,activator of Hsp90 ATPase homolog 1, Activator of HSP90 ATPase Activity 1), inhibits interaction between Hsp90 and Aha1.
    KU-177 inhibits Hsp90-mediated luciferase refolding activity in PC3-MM2 cell with IC50 of 2 uM.
    KU-177 inhibits Aha1 enhancement of Hsp90-mediated tau aggregation, increased soluble, phosphorylated tau in cultured cells.
    AHSA1-K137 is identified as the site-specific targeting of KU-177 and Bufalin.
    KU-177 decreases MM cell proliferation and proteasome inhibitor (PI) resistance induced by AHSA1/HSP90 in vitro (H929 cell IC50=25.8 uM).
    KU-177 (1mg/kg, twice per week) extends the survival of 5TMM3VT MM mice when combined with Bortezomib (BTZ) (1mg/kg, twice per week).

    Physicochemical Properties

    M.Wt 489.48
    Formula C27H23NO8
    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

    3-(3',6-dimethoxy-[1,1'-biphenyl]-3-carboxamido)-8-methoxy-2-oxo-2H-chromen-7-yl acetate

    References

    1. Shelton LB, et al. Proc Natl Acad Sci U S A. 2017 Sep 5;114(36):9707-9712.

    2. Gu C, et al. J Exp Clin Cancer Res. 2022 Jan 6;41(1):11.

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