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首页-小分子抑制剂&激动剂-JAK/STAT Signaling-STAT-BP-5-087
BP-5-087

Chemical Structure : BP-5-087

CAS No.: 1803281-30-2

BP-5-087 (BP 5-087)

货号: PC-61260Not For Human Use, Lab Use Only.

BP-5-087 is a potent, selective STAT3 SH2 domain inhibitor (EC50=5.6 uM) that reduces STAT3 phosphorylation and nuclear transactivation.

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

    生物&药学活性

    BP-5-087 is a potent, selective STAT3 SH2 domain inhibitor (EC50=5.6 uM) that reduces STAT3 phosphorylation and nuclear transactivation.
    BP-5-087 restores TKI sensitivity to therapy-resistant CML progenitor cells in primary cells from CML patients with BCR-ABL1 kinase-independent TKI resistance, including leukemic stem cells.

    物理化学性质&存储条件

    分子量 770.691
    分子式 C36H30F8N2O6S
    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

    4-(N-(4-cyclohexylbenzyl)-2-((N-((perfluorophenyl)methyl)-4-(trifluoromethyl)phenyl)sulfonamido)acetamido)-2-hydroxybenzoic acid

    参考文献

    1. Eiring AM, et al. Leukemia. 2015 Mar;29(3):586-597.

    2. Eiring AM, et al. Leuk Suppl. 2014 Dec;3(Suppl 1):S5-6.

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