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SU1498,168835-82-3

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  • ¥765
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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.

    • 英文名

      AG 1498; Tyrphostin SU 1498

    • 库存

      货期:1-2天

    • 供应商

      MedChemExpress LLC

    • 规格

      5 mg

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    SU1498

    CAS No. : 168835-82-3

    MCE 国际站:SU1498

    产品活性:SU1498 (AG 1498) 是选择性的 VEGFR2 抑制剂;抑制 Flk-1IC50 值为 700 nM。

    研究领域:Protein Tyrosine Kinase/RTK

    作用靶点:VEGFR

    In Vitro: SU1498 stimulates accumulation of phosphorylated ERKs in human umbilical vein endothelial cells and in human aortic endothelial cells in a manner that is dependent on the functioning of the upstream components of the MAPK pathway, B-Raf, and MEK kinases. The enhanced accumulation of phospho-ERKs is observed only in cells that have been stimulated with sphingosine 1-phosphate or protein growth factors; SU1498 by itself is ineffective. SU1498 blocks signal transduction from VEGFR2 in MS1 VEGF cells.In the presence of SU1498, levels of Ets-1 are decreased, suggesting that VEGF-VEGFR-2 interactions contributed to baseline levels of Ets-1 expression, and interruption of this autocrine interaction with SU1498 led to decreased expression of Ets-1. SU1498 treatment significantly impacts U87 cell proliferation and apoptosis. SU1498 induces a marked increase in lipids and a decrease in glycerophosphocholine. Accordingly, accumulation of lipid droplets is seen in the cytoplasm of SU1498-treated U87 cells.

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