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RX-375

Chemical Structure : RX-375

CAS No.:

RX-375 (RX375, RX 375)

Catalog No.: PC-20473Not For Human Use, Lab Use Only.

RX-375 (RX375) is an indirect small-molecule activator of AMPK by directly binds to Prohibitins (PHB1 and PHB2), induces dissociation of AMPK-PHBs complex.

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    Biological Activity

    RX-375 (RX375) is an indirect small-molecule activator of AMPK by directly binds to Prohibitins (PHB1 and PHB2), induces dissociation of AMPK-PHBs complex.
    RX-375 does not activate recombinant AMPK proteins composed of α1β1γ1 or α2β1γ1 subunits in vitro at 100 uM.
    RX-375 inhibits fatty acid synthesis in HepG2 cells in a PPARα-independent manner, 10,000 times more potent than metformin.
    RX-375 exhibits stimulatory and inhibitory effects on AMPKα phosphorylation and fatty acid synthesis, respectively, in primary human hepatocytes.
    RX-375 attenuates the interaction between AMPK and PHBs, PHBs are negative regulators of AMPK.
    RX-375 (30 mg/kg, oral) increasees AMPKα phosphorylation level, reduces triglyceride content and inhibits fatty acid synthesis in the liver of obese mice.

    Physicochemical Properties

    M.Wt 407.45
    Formula C23H22FN3O3
    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-((1-ethylureido)methyl)-N-(4-(4-fluorophenoxy)phenyl)benzamide

    References

    1. Kanagaki S, et al. iScience. 2023 Feb 28;26(4):106293.

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