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    Amlexanox 68302-57-8

    簡要描述:Amlexanox 68302-57-8
    Amlexanox (AA673; CHX3673) is a specific inhibitor of IKKε and TBK1; inhibition of IKKε and TBK1 activity as determined by MBP phosphorylation showing an IC50 of approximately 1–2

    • 產(chǎn)品型號:abs47027799
    • 廠商性質(zhì):生產(chǎn)廠家
    • 更新時間:2025-12-30
    • 訪  問  量:677

    詳細介紹

    品牌absinCAS68302-57-8
    分子式C15H14N2O4純度>98%
    分子量298.29貨號abs47027799
    規(guī)格10mg供貨周期現(xiàn)貨
    主要用途is a specific inhibitor應(yīng)用領(lǐng)域化工,生物產(chǎn)業(yè),農(nóng)林牧漁,制藥/生物制藥,綜合

    Amlexanox 68302-57-8

    產(chǎn)品描述
    描述

    Amlexanox (AA673; CHX3673) is a specific inhibitor of IKKε and TBK1; inhibition of IKKε and TBK1 activity as determined by MBP phosphorylation showing an IC50 of approximately 1–2 μM.

    純度
    >98%
    儲存/保存方法
    Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.
    基本信息
    別名
    氨lai呫諾;AA673;Amoxanox;CHX3673
    外觀
    white to beige powder
    可溶性/溶解性
    DMSO : 100 mg/mL(335.24 mM)
    生物活性
    靶點
    TBK1 ,IKK-ε
    In vitro(體外研究)
    Dose-response relationship of amlexanox inhibition of IKK-? and TBK1 activity as determined by MBP phosphorylation showing an IC50 of approximately 1-2 μM. Amlexanox also blocks the activity of TBK1 at approximately the same concentrations but has no effect on IKK-α or IKK-β and at these concentrations do not block any other kinases from a broad panel representing most kinase families. Inhibition of IKK-? or TBK1 by amlexanox is competitive for its substrate ATP, indicating that it interacts with the enzymes in the ATP-binding site. Amlexanox increases the phosphorylation of TBK1 at Ser172 in 3T3-L1 adipocytes and blocks polyinosinic:polycytidylic acid (poly I:C)-stimulated phosphorylation of interferon responsive factor-3 (IRF3), a presumed substrate of IKK-? and TBK1.
    In vivo(體內(nèi)研究)
    Treatment of obese mice with amlexanox elevates energy expenditure through increased thermogenesis, producing weight loss, improves insulin sensitivity and decreases steatosis.
    研究領(lǐng)域
    研究領(lǐng)域
    CancerOncoproteins/suppressorsOncoproteinsSignal transducers
    CancerSignal transductionProtein phosphorylationSerine/threonine kinasesOther
    EpigeneticsCell cycleKinases/PhosphatasesOther
    ImmunologyInnate ImmunityTLR Signaling
    Signal TransductionProtein PhosphorylationSer / Thr KinasesOther Kinases
    Drug DiscoverySmall Molecule DrugLead Compound Discovery
    Amlexanox 68302-57-8溫馨提示:本產(chǎn)品僅作科研實驗使用,不支持臨床等研究

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