
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)






规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥275 | 有现货 |
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5MG | ¥446 | 有现货 |
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10MG | ¥721 | 有现货 |
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25MG | ¥1320 | 有现货 |
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50MG | ¥2001 | 有现货 |
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100MG | ¥2989 | 有现货 |
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200MG | ¥4447 | 有现货 |
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500MG | 获取报价 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Fasentin
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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
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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)。
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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.
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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.
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体内实验——
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同义词Fasentin
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通路Membrane Transporter/Ion Channel
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靶点GLUT
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受体GLUT
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研究领域——
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适应症——
化学信息
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CAS Number392721-37-8
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分子量279.643
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分子式C11H9ClF3NO2
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 100 mg/mL (357.60 mM)
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SMILESCC(CC(NC1=CC=C(Cl)C(C(F)(F)F)=C1)=O)=O
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化学全称N-[4-Chloro-3-(trifluoromethyl)phenyl]-3-oxobutanamide
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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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.