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- 详细信息
- 文献和实验
- 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
- CAS号:
473-15-4
- 规格:
1 mg/5 mg/10 mg/25 mg/50 mg
| 规格: | 1 mg | 产品价格: | ¥600.0 |
|---|---|---|---|
| 规格: | 5 mg | 产品价格: | ¥1400.0 |
| 规格: | 10 mg | 产品价格: | ¥2200.0 |
| 规格: | 25 mg | 产品价格: | ¥3600.0 |
| 规格: | 50 mg | 产品价格: | ¥5000.0 |
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Beta-Eudesmol
CAS No. : 473-15-4
MCE 国际站:Beta-Eudesmol
产品活性:Beta-Eudesmol 具有抗癌、抗炎活性。Beta-Eudesmol 能够诱导细胞凋亡。Beta-Eudesmol 可以拮抗新斯的明诱导的神经肌肉衰竭。Beta-Eudesmol 可以用于脓毒症、神经肌肉衰竭等疾病的研究。Beta-Eudesmol 是可以从苍术的根茎中提取得到的类倍半萜烯化合物。
研究领域:Apoptosis | Immunology/Inflammation | Metabolic Enzyme/Protease | NF-κB
作用靶点:Caspase | TNF Receptor | SOD | Reactive Oxygen Species
In Vitro: Beta-Eudesmol (30-100 μM; 6 days) can inhibit the cell proliferation induced by vascular endothelial growth factor (VEGF) (30 ng/ml) and basic fibroblast growth factor (bFGF) (30 ng/ml) in HUVEC cells, thereby inhibiting angiogenesis.
Beta-Eudesmol (10-100 μM; 72 h) inhibits cell proliferation in a time- and dose-dependent manner in tumor in tumer cells HeLa, SGC-7901 and BEL-7402.
Beta-Eudesmol (10-120 μM; 4 h) can reduce cell activity in HL-60 cells.
Beta-Eudesmol (40-80 μM; 4 h) can activate caspase-3 by inducing the release of cytochrome c, thereby inducing cell apoptosis in HL-60 cells.
In Vivo: Beta-Eudesmol (2.5-5 mg/kg; Intraperitoneal injection; Once daily for 7 days) significantly inhibits tumor cell and new blood vessel generation in MK mice.
Beta-Eudesmol (50-100 mg/kg; Intraperitoneal injection; Single dose) can inhibit the NF-κb signaling pathway and has anti-inflammatory and antioxidant effects in C57BL/6 mice.
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文献和实验(Ser645) expression, andincreases in the total level of β-catenin and glycogen synthase protein expression were observed . 1.1.1. Inorganic Elements as Inhibitors of GSK-3 Lithium was the first discovered GSK-3 inhibitor (15
医生和球 看的文献较少,自己知道的只有wnt、PTEN等,请问还有哪些通路与β-catenin有关,有无类似的综述?谢谢! 狐狸renart 只知道wnt chuckdouble The canonical Wnt/beta-catenin signalling pathway. Barker N. Methods Mol Biol. 2008;468:5-15
真爱满行囊 我最近在体外细胞做的关于gsk3-beta功能问题,发现药物处理以后,gsk-3-beta的总表达量下调,如果是这样的话 1、我是否能够得出gsk-3-beta的活性下调的结论? 2、是否还有必要做非活性形式的表达量?我的理解是,基础状态下,gsk-3beta维持的是低活性状态,如果总量都下调了,那应该能够得出活性降低的结论了吧? 3、另外,在这种情况下我是否有必要去做gsk-3-beta的216位点的活性形式的表达
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