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F16

CAS No. 36098-33-6

F16 ( (E)-4-(3-indolylvinyl)-N-methylpyridinium iodide )

产品货号. M26683 CAS No. 36098-33-6

F16 抑制 neu 过表达细胞的生长和乳腺上皮的增殖。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥267 有现货
10MG ¥432 有现货
25MG ¥849 有现货
50MG ¥1469 有现货
100MG ¥1917 有现货
200MG ¥2871 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 ¥466 有现货

生物学信息

  • 产品名称
    F16
  • 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
    F16 抑制 neu 过表达细胞的生长和乳腺上皮的增殖。
  • 产品描述
    F16 inhibits the growth of neu-overexpressing cells and the proliferation of mammary epithelial.(In Vitro):F16 arrests the cell cycle and increases apoptosis in F16-sensitive EpH4-A6 cells. F16 (3 μM) influences growth in human and mice cancer cell lines. F16 shows mitochondriotoxic property and triggers apoptosis or necrosis depending on the genetic background of the target carcinoma cell.
  • 体外实验
    F16 (3 μM; 3 days/7 days) affects growth in several mouse and human cancer cell lines.F16 arrests cell cycle and increases apoptosis in F16-sensitive EpH4-A6 cells. Cell Proliferation Assay Cell Line:MDA-MB231, MDA-MB435, MDA-MB436, MDA-MB453, MDA-MB-468, SKBR-3, MCF-7, T47D, ZR-75-1 cells and mouse mammary epithelial cell line NMuMGConcentration:3 μM Incubation Time:3 days/7 days Result:Displayed antiproliferative activity against both mouse and human breast cancer cells. The growth of the mouse fibrosarcoma cell lines derived from ras-transgenic mice was not affected.
  • 体内实验
    ——
  • 同义词
    (E)-4-(3-indolylvinyl)-N-methylpyridinium iodide
  • 通路
    Others
  • 靶点
    Other Targets
  • 受体
    IGF-1R| P-Akt (S473)| P-Akt (T308)| S6 Kinase
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    36098-33-6
  • 分子量
    362.21
  • 分子式
    C16H15IN2
  • 纯度
    >98% (HPLC)
  • 溶解度
    In Vitro:?DMSO : ≥ 31 mg/mL (85.59 mM)
  • SMILES
    [I-].C[n+]1ccc(\C=C\c2c[nH]c3ccccc23)cc1
  • 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.Wang X, et al. Diffusion basis spectrum imaging detects and distinguishes coexisting subclinical inflammation, demyelination and axonal injury in experimental autoimmune encephalomyelitis mice. NMR Biomed. 2014 Jul;27(7):843-52.
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