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- 详细信息
- 技术资料
- 保存条件:
-20°C, stored under nitrogen
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- 规格:
10 mM * 1 mL/1 mg/5 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥4620.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥2045.0 |
| 规格: | 5 mg | 产品价格: | ¥4500.0 |
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FTI-2153
CAS No. : 344900-92-1
MCE 国际站:FTI-2153
产品活性:FTI-2153 是一种有效、高度选择性的法尼基转移酶 farnesyltransferase (FTase) 抑制剂,IC50 为 1.4 nM。FTI-2153 有效抑制 H-Ras 蛋白的加工修饰,IC50 值为 10 nM,对其抑制活性是对 Rap1A 蛋白加工的 3000 多倍。
研究领域:Metabolic Enzyme/Protease
作用靶点:Farnesyl Transferase
In Vitro: FTI-2153, inhibits bipolar spindle formation during mitosis in two human lung cancer cell lines.
?FTI-2153 increases the percentage of prometaphase cells with ring-like DNA morphology in transformed and non-transformed cells.
?FTI-2153 (15 μM) inhibits T-24 and Calu-1 cell growth by 38 and 36%, respectively. NIH3T3, HFF and HT-1080 are less sensitive and are inhibited by only 8, 8 and 13%, respectively. A-549 and OVCAR3 cell growth is inhibited by 25 and 22%, respectively. Thus, even though T-24 and Calu-1 cells are equisensitive to FTI-2153 cell growth inhibition, FTI-2153 inhibits bipolar spindle formation only in Calu-1 cells. HFF and NIH3T3 cells are both resistant to FTI2153 growth inhibition, yet only NIH3T3 cells are resistant to FTI-2153 inhibition of bipolar spindle formation.
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