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FAK Inhibitor 14

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  • Cayman已认证
  • USA
  • 14485
  • 2025年07月09日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 供应商

      Neobioscience

    • 保存条件

      -20

    • 规格

      1 g

    A direct inhibitor of FAK1 autophosphorylation, blocking phosphorylation of Y397 (IC50 = 1 μM); no known significant effect on the activity of a range of other kinases; promotes cell detachment and inhibits cell adhesion of cells in culture; blocks tumor growth in vivo

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    图标文献和实验
    相关实验
    • 14-3-3 proteins

      14-3-3 is a potent inhibitor of protein kinase C, but the N-terminal domain does not inhibit PKC activity. Site-specific mutagenesis of several regions in the tau isoform of 14-3-3, including the mutation of a putative pseudosubstrate site

    • Introduction of human 14-3-3 proteins

      inhibitor of protein kinase C,but the N-terminal domain does not inhibit PKC activity.Site-specific mutagenesis of several regions in the tau isoform of 14-3-3,including the mutation of a putative pseudosubstrate site to a potential substrate sequence

    • Methods for Studying the Interaction of Barnase with Its Inhibitor Barstar

      complex, with K d =10−14 M , half-life of about 2 d and an association rate constant of 4�108 M −1 /s. The kinetic and thermodynamics of the barnase-barstar interaction were investigated in detail (12 –20 ). High affinity is maintained at pH 7.0–

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