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首页-小分子抑制剂&激动剂-PI3K/Akt/mTOR Pathway-PI3K-ST-168
ST-168

Chemical Structure : ST-168

CAS No.: 2126038-25-1

ST-168 (ST168)

货号: PC-61741Not For Human Use, Lab Use Only.

ST-168 is a novel potent, orally available MEK/PI3K bifunctional inhibitor with IC50 of 182, 69.2, 1482, 2293, and 41.7 nM for MEK1, PI3Kα, PI3Kβ, PI3Kγ, and PI3Kδ, respectively.

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

    生物&药学活性

    ST-168 is a novel potent, orally available MEK/PI3K bifunctional inhibitor with IC50 of 182, 69.2, 1482, 2293, and 41.7 nM for MEK1, PI3Kα, PI3Kβ, PI3Kγ, and PI3Kδ, respectively.
    ST-168 exhibits improved inhibition toward PI3K isoforms compared to ST-162.
    ST-168 demonstrates superior tumoricidal efficacy over ST-162 in an A375 melanoma spheroid tumor model.

    物理化学性质&存储条件

    分子量 1010.762
    分子式 C41H44F5IN10O7
    外观性状 Solid
    CAS No.
    储存条件
    固体粉末
    -20 °C 12 个月; 4°C 6 个月
    配置液
    -80 °C 6 个月; -20°C 6 个月
    Shipping
    Solubility

    10 mM in DMSO

    Chemical Name/SMILES

    N-(2-(2-(2-(3-(4-(4-(2-(difluoromethyl)-1H-benzo[d]imidazol-1-yl)-6-morpholino-1,3,5-triazin-2-yl)piperazin-1-yl)-3-oxopropoxy)ethoxy)ethoxy)ethoxy)-3,4-difluoro-2-((2-fluoro-4-iodophenyl)amino)benzamide

    参考文献

    1. Van Dort ME, et al. ACS Med Chem Lett. 2017 Jul 24;8(8):808-813.

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