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HTH-01-015,1613724-42-7

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  • ¥363 - 4850
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  • 2025年12月05日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 保存条件

      Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.

    • 库存

      货期:1-2天

    • 供应商

      MedChemExpress LLC

    • CAS号

      1613724-42-7

    • 规格

      10 mM * 1 mL/1 mg/5 mg/10 mg/50 mg/100 mg

    规格:10 mM * 1 mL产品价格:¥880.0
    规格:1 mg产品价格:¥363.0
    规格:5 mg产品价格:¥800.0
    规格:10 mg产品价格:¥1200.0
    规格:50 mg产品价格:¥3600.0
    规格:100 mg产品价格:¥4850.0

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    HTH-01-015

    CAS No. : 1613724-42-7

    MCE 国际站:HTH-01-015

    产品活性:HTH-01-015 是一种选择性 NUAK1/ARK5 抑制剂 (IC50 为 100 nM)。HTH-01-015 抑制 NUAK1 的效力比抑制 NUAK2 高 100 倍以上 (IC50>10 μM)。

    研究领域:Epigenetics  |  PI3K/Akt/mTOR

    作用靶点:AMPK

    In Vitro: HTH-01-015 is a specific NUAK1 inhibitor. The related NUAK1 and NUAK2 are members of the AMPK (AMP-activated protein kinase) family of protein kinases that are activated by the LKB1 (liver kinase B1) tumor suppressor kinase. HTH-01-015 inhibits NUAK1 with an IC50 of 100 nM, but does not significantly inhibit NUAK2 (IC50 of >10 μM).? In all cell lines tested, HTH-01-015 inhibits the phosphorylation of the only well-characterized substrate, MYPT1 (myosin phosphate-targeting subunit 1) that is phosphorylated by NUAK1 at Ser445. In U2OS cells, HTH-01-015 suppresses proliferation and phosphorylation of MYPT1 to the same extent as shRNA-mediated NUAK1 knockdown. In mouse embryonic fibroblasts (MEFs), treatment with 10 μM HTH-01-015 suppresses proliferation and phosphorylation of MYPT1 to the same extent as NUAK1-knockout. To test whether NUAK1 inhibition impaired the ability of the invasive U2OS cells to enter a matrix, 3D Matrigel Transwell invasion assays demonstrate that 10 μM HTH-01-015 markedly inhibits the invasiveness of U2OS cells in this assay.

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