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BT317

Chemical Structure : BT317

CAS No.: 2334093-39-7

BT317 (BT 317)

Catalog No.: PC-20757Not For Human Use, Lab Use Only.

BT317 is a small molecule dual inhibitor of mitochondrial Lon Peptidase 1 (LonP1) and CT-L proteasome, subsequently induces ROS accumulation and autophagy-dependent cell death in high-grade IDH1 mutated astrocytoma lines.

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    Biological Activity

    BT317 is a small molecule dual inhibitor of mitochondrial Lon Peptidase 1 (LonP1) and CT-L proteasome, subsequently induces ROS accumulation and autophagy-dependent cell death in high-grade IDH1 mutated astrocytoma lines.
    BT317 inhibits LonP1 protease activity with IC50 of 58.15 uM.
    BT317 exhibits synergy with temozolomide in autophagy-dependent cell death in IDH1 mutant malignant astrocytoma.
    BT317 is selective to the tumor microenvironment and demonstrated therapeutic efficacy both as a single agent and in combination TMZ in IDH mutant astrocytoma models.

    Physicochemical Properties

    M.Wt 315.71
    Formula C16H10ClNO4
    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

    6-chloro-N-(4-hydroxyphenyl)-2-oxo-2H-chromene-3-carboxamide

    References

    1. Douglas C, et al. bioRxiv. 2023 Apr 17:2023.04.13.536816.

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