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Fasentin

CAS No. 392721-37-8

Fasentin ( Fasentin )

产品货号. M14350 CAS No. 392721-37-8

Fasentin 是一种新型葡萄糖摄取 (GLUT) 抑制剂,可使癌细胞对 FAS 诱导的细胞死亡敏感,与 GLUT1 相比,优先抑制 GLUT4 (IC50=68 uM)。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
2MG ¥275 有现货
5MG ¥446 有现货
10MG ¥721 有现货
25MG ¥1320 有现货
50MG ¥2001 有现货
100MG ¥2989 有现货
200MG ¥4447 有现货
500MG 获取报价 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    Fasentin
  • 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
    Fasentin 是一种新型葡萄糖摄取 (GLUT) 抑制剂,可使癌细胞对 FAS 诱导的细胞死亡敏感,与 GLUT1 相比,优先抑制 GLUT4 (IC50=68 uM)。
  • 产品描述
    Fasentin is a novel inhibitor of glucose uptake (GLUT) that sensitizes cancer cells to FAS-induced cell death, preferentially inhibits GLUT4 (IC50=68 uM) over GLUT1; sensitizes cancer cells to the death ligands FAS and TNF apoptosis-inducing ligand, and induces G1 cell cycle arrest.
  • 体外实验
    Fasentin (0.1-1000 μM; 72?hours) inhibits endothelial, tumour and fibroblast cell growth without inducing cell death. Fasentin (25-100 μM; 16-24 hours) induces a cell cycle arrest in G0/G1 phase and reduces the cell number in S phase in a dose-dependent manner. Fasentin (50 μM; 16 hours) alters expression of genes associated with glucose deprivation such as AspSyn and PCK-2.Fasentin (15, 30, 80 μM; pretreatment 1 hour) induces glucose deprivation, partially blocks glucose uptake in PPC-1, DU145, and U937 cells. Fasentin (100 μM; 16 hours) does not affect the migratory capability of endothelial cells. Fasentin (25-100 μM; 16?hours) lowers levels of phospho-ERK in HMECs, indicating a partial inhibition on the ERK signalling pathway, even though the effect is not statistically significant. Fasentin does not inhibit the tyrosine kinase activity of VEGFR2. Fasentin interacts with a unique site in the intracellular channel of GLUT1. Cell Viability Assay Cell Line:Three types of endothelial cells ECs (HMEC, human microvascular endothelial cells; HUVEC, human umbilical vein endothelial cells; and BAEC, bovine aortic endothelial cells), three human tumour cell lines (MDA-MB-231 and MCF7 breast carcinoma cells, and HeLa cervix adenocarcinoma cells), and human gingival fibroblasts (HGF)Concentration:0.1, 1, 10, 100, 1000 μM Incubation Time:72?hours Result:Inhibited endothelial, tumour and fibroblast cell growth (IC50=26.3-111.2 μM) without inducing cell death.Cell Cycle Analysis Cell Line:HMECs Concentration:25, 50, 100 μM Incubation Time:16, 24 hours Result:Induced a cell cycle arrest in G0/G1 phase and reduced the cell number in S phase in a dose-dependent manner.Incubation Time:16 hours Result:Altered expression of genes associated with glucose deprivation such as AspSyn and PCK-2 not FLIP mRNA expression.
  • 体内实验
    ——
  • 同义词
    Fasentin
  • 通路
    Membrane Transporter/Ion Channel
  • 靶点
    GLUT
  • 受体
    GLUT
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    392721-37-8
  • 分子量
    279.643
  • 分子式
    C11H9ClF3NO2
  • 纯度
    >98% (HPLC)
  • 溶解度
    In Vitro:?DMSO : 100 mg/mL (357.60 mM)
  • SMILES
    CC(CC(NC1=CC=C(Cl)C(C(F)(F)F)=C1)=O)=O
  • 化学全称
    N-[4-Chloro-3-(trifluoromethyl)phenyl]-3-oxobutanamide

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. Wood TE, et al. Mol Cancer Ther. 2008 Nov;7(11):3546-55. 2. Schimmer AD, et al. Cancer Res. 2006 Feb 15;66(4):2367-75. 3. Granchi C, et al. Medchemcomm. 2016 Sep 1;7(9):1716-1729.
产品手册
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