• merck millipore,默克密理博,539644,UCN-01
  • merck millipore,默克密理博,539644,UCN-01

    产品名称:UCN-01
    产品型号:539644
    A cell-permeable Staurosporine derived anticancer agent that reversibly and ATP-competitively inhibits several protein kinases.

    merck millipore,默克密理博,539644,UCN-01

  • 产品介绍

  • 重要规格表

    经验配方 CAS号
    C₂₈H₂₆N₄O₄112953-11-4
    描述
    概述 A cell-permeable Staurosporine (Cat. No. 569397) derived anticancer agent that reversibly and ATP-competitively inhibits several protein kinases (IC50 = 29 nM, 34 nM, 30 nM, 590 nM and 530 nM for PKCα, PKCβ, PKCγ, PKCδ and PKCε; IC50 = 7 nM, 27 nM, 50 nM, 50 nM, 150 nM and 1.04 µM for Chk1, Cdc25C-associated protein kinase 1, Cdk1, PAK4, Cdk5/p25 and Chk2; IC50 = 33 nM, 50 nM, 95 nM, 500 nM, 500 nM and 1.0 µM for PDK1, lck, MAPKAP kinase-2, Akt, GSK-3β and PKA, respectively). At higher concentrations (> 15 µM), affects the activities of Src, PIM-1, CKII, DNA-PK, ErK1, ILK-1 and MAPKK1). Reported to suppress thymidylate synthase expression, induce apoptosis with caspase activation, and sensitize tumor cells to a range of DNA-damaging agents.
    产品目录编号 539644
    品牌系列 Calbiochem®
    同义词 7-Hydroxystaurosporine, Staurosporine, 7β-Hydroxy, Streptomyces sp., Chk1 Inhibitor VI, Chk2 Inhibitor V
    参考
    参考 Reinhardt, H.C., et al. 2007. Cancer Cell 11, 175.
    Jiang, X., et al. 2004. Mol. Cancer Ther. 3, 1221.
    Sato, S., et al. 2002. Oncogene 21, 1727.
    Patel, V., et al. 2002. Clin. Cancer Res. 8, 3549.
    Leclerc, S., et al. 2001. J. Biol. Chem. 276, 251.
    Busby, E.C., et al. 2000. Cancer Res. 60, 2108.
    Hsueh, C.T., et al. 1998. Clin. Cancer Res. 4, 2201.
    Akiyama, T., et al. 1997. Cancer Res. 57, 1495.
    Seynaeve, C.M., et al. 1994. Mol. Pharmacol. 45, 1207.
    Takahashi, I., et al. 1987, J. Antibiot. 40, 1782.
    产品信息
    CAS号 112953-11-4
    具有ATP竞争性 Y
    形式 Tan solid
    Hill配方 C₂₈H₂₆N₄O₄
    化学配方 C₂₈H₂₆N₄O₄
    Molar Mass 482.5
    可逆 Y
    结构配方图像
    生物信息
    主靶 PKCα, PKCβ, PKCγ, PKCδ PKCε, Chk1, Cdc25C-associated protein kinase 1, Cdk1, PAK4, Cdk5/p25 and Chk2, PDK1, lck, MAPKAP kinase-2, Akt, GSK-3β and PKA
    主靶IC50 IC50 = 29 nM, 34 nM, 30 nM, 590 nM, 530 nM, 7 nM, 27 nM, 50 nM, 50 nM, 150 nM, 1.04 µM, 33 nM, 50 nM, 95 nM, 500 nM, 500 nM and 1.0 µM, respectively for primary targets in the order listed
    纯度 ≥95% by HPLC
    理化信息
    细胞可渗透 Y
    溶解度 DMSO or EtOH
    储存和货运信息
    货运代码 Ambient Temperature Only
    毒性 Standard Handling
    储存 +2°C to +8°C
    避光 Protect from light
    无需冷冻 No
    特殊指南 Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 6 months at -20°C.
    包装信息
    惰性气体下包装 Packaged under inert gas


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