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IPR-179

Chemical Structure : IPR-179

CAS No.: 2098556-70-6

IPR-179 (ACT-03, IPR179)

Catalog No.: PC-72035Not For Human Use, Lab Use Only.

IPR-179 (ACT-03) is a potent, BBB-permeable, selective gelatinase (MMP2 and MMP9) inhibitor with IC50 of 656 nM and 310 nM, respectively.

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

    Biological Activity

    IPR-179 (ACT-03) is a potent, BBB-permeable, selective gelatinase (MMP2 and MMP9) inhibitor with IC50 of 656 nM and 310 nM, respectively.
    IPR-179 dispalys high selectivity over MMP1/3/7/8, ADAM10/17, Prolyl oligopeptidase and DPP4 (IC50=3.3 uM->20 uM).
    IPR-179 reduced seizure severity in the rapid-kindling rat model.
    IPR-179 reduced the number of spontaneous seizures in the kainic acid model (during and up to 7 weeks after delivery) without side effects while improving cognitive behavior.
    IPR-179 prevented an MMP2/9-dependent switch-off normally restraining network excitability during the activity period.

    Physicochemical Properties

    M.Wt 631.67
    Formula C29H41F4N5O6
    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

    (R)-N-((2S,3R)-1-(((S)-4-(3,5-difluorobenzamido)-1-(hydroxyamino)-1-oxobutan-2-yl)amino)-3-methyl-1-oxopentan-2-yl)-4,4-difluoro-1-hexanoyl-N-methylpyrrolidine-2-carboxamide

    References

    1. Diede Wm Broekaart, et al. J Clin Invest. 2021 Jan 4;131(1):e138332.

    2. Alexandra Bertran, et al. Bioorg Chem. 2020 Jan;94:103365.

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