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LCH-7749944

CAS No. 796888-12-5

LCH-7749944 ( GNF-PF-2356 )

产品货号. M22466 CAS No. 796888-12-5

LCH-7749944通过下调PAK4/c-Src/EGFR/cyclin D1通路有效抑制人胃癌细胞的增殖并诱导细胞凋亡。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥929 有现货
10MG ¥1349 有现货
25MG ¥2213 有现货
50MG ¥3162 有现货
100MG ¥4275 有现货
200MG ¥5751 有现货
500MG 获取报价 有现货
1G 获取报价 有现货
1 mL x 10 mM in DMSO ¥1007 有现货

生物学信息

  • 产品名称
    LCH-7749944
  • 注意事项
    本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
  • 产品简述
    LCH-7749944通过下调PAK4/c-Src/EGFR/cyclin D1通路有效抑制人胃癌细胞的增殖并诱导细胞凋亡。
  • 产品描述
    LCH-7749944 effectively suppresses the proliferation of human gastric cancer cells through downregulation of PAK4/c-Src/EGFR/cyclin D1 pathway and induces apoptosis.?LCH-7749944 is a potent PAK4 inhibitor with an IC50 of 14.93 μM.?LCH-7749944 (5-20 μM; 12-48 hours) prominently induces a dose-dependent increase in the percentage of cells in G1 phase and decrease in S phase. ?LCH-7749944 (5-30 μM; 24 hours) dramatically decreases levels of phosphoPAK4, phospho-c-Src, phospho-EGFR and cyclin D1 protein expression in a dose-dependent manner.?LCH-7749944 (GNF-PF-2356;?5-50 μM;?24 hours) inhibits the proliferation of MKN-1, BGC823, SGC7901 and MGC803 cells in a concentration dependent manner.??LCH-7749944 (5-20 μM;?12-48 hours) induces apoptosis of SGC7901 cells.??
  • 体外实验
    Cell Proliferation Assay Cell Line:MKN-1, BGC823, SGC7901 and MGC803 human gastric cancer cells Concentration:5, 10, 15, 20, 25, 30, 35, 40, 45, 50 μM Incubation Time:24 hoursResult:Inhibited the proliferation of MKN-1, BGC823, SGC7901 and MGC803 cells in a concentration dependent manner.Apoptosis Analysis Cell Line:SGC7901 cells Concentration:5, 10, 20 μM Incubation Time:12, 24, 48 hours Result:Induced apoptosis of SGC7901 cells.Cell Cycle Analysis Cell Line:SGC7901 cells Concentration:5, 10, 20 μM Incubation Time:12, 24, 48 hours Result:Prominently induced a dose-dependent increase in the percentage of cells in G1 phase and decrease in S phase.Western Blot AnalysisCell Line:SGC7901 cells Concentration:5, 10, 20, 30 μM Incubation Time:24 hours Result:Dramatically decreased levels of phosphoPAK4, phospho-c-Src, phospho-EGFR and cyclin D1 protein expression in a dose-dependent manner.
  • 体内实验
    ——
  • 同义词
    GNF-PF-2356
  • 通路
    Apoptosis
  • 靶点
    Apoptosis
  • 受体
    PAK4|apoptosis
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    796888-12-5
  • 分子量
    350.41
  • 分子式
    C20H22N4O2
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO:250 mg/mL (713.45 mM; Need ultrasonic)
  • SMILES
    COc1cccc(Nc2nc(NCC3CCCO3)c3ccccc3n2)c1
  • 化学全称
    ——

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

1. Zhang J, et al. LCH-7749944, a novel and potent p21-activated kinase 4 inhibitor, suppresses proliferation and invasion in human gastric cancer cells. Cancer Lett. 2012 Apr 1;317(1):24-32.
产品手册
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