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  • ML-265

    • TEPP-46
    货号: abs814095
    CAS号: 1221186-53-3
    分子式: C17H16N4O2S2
    分子量: 372.5
    产品说明书
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    货号-规格 货期 价格 数量
    abs814095-50mg 现货 ¥4912.00
    - +
    abs814095-100mg 现货 ¥7095.00
    - +
    大包装询价
    产品描述
    描述
    ML-265 activates tumor-specific PKM2 (EC50 = 92 nM) by binding to the dimer-dimer interface between two subunits of PKM2 and inducing tetramerization.
    纯度
    >98%
    储存/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
    别名
    TEPP-46
    外观
    White to off white powder
    可溶性/溶解性
    DMSO : 50 mg/mL (134.24 mM; Need ultrasonic)
    生物活性
    靶点
    Pyruvate Kinase
    In vitro(体外研究)
    TEPP-46 and DASA-58 activate PKM2 by a mechanism similar to that of the endogenous activator FBP. Pre-treatment of cells with TEPP-46 or DASA-58 prevents pervanadate-induced inhibition of PKM2 activity. TEPP-46 also induces a decrease in the intracellular levels of acetyl-coA, lactate, ribose phosphate and serine. TEPP-46 inhibits LPS-induced Hif-1α and IL-1β, as well as the expression of a range of other Hif-1α-dependent genes. TEPP-46 treatment significantly downregulates the expression of the M1 markers Il12p40 and Cxcl-10. Activation of PKM2 using TEPP-46 significantly inhibits FSL-1 and CpG-induced Il1b mRNA expression. TEPP-46 inhibits Mtb-induced Il1b mRNA levels, boosts Mtb-induced levels of Il10 mRNA, and has no effect on levels of Tnf.
    In vivo(体内研究)
    TEPP-46 exhibits good oral bioavailability with relatively low clearance, long half-life, and good volume of distribution-parameters that predict for drug exposure in tumor tissues. TEPP-46 at 150 mg/kg readily achieves maximal PKM2 activation measured in A549 xenograft tumors.
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