Rsva 405 ≥98%
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| 包装规格: | 1mg 5mg 10mg 25mg 50mg 100mg in glass bottle |
| 产品简介: | RSVA405 是一种有效和具有口服活性的 AMPK 激活剂,EC50 值为 1 μM。RSVA405 通过促进 CaMKKβ 依赖的 AMPK 活化,从而抑制 mTOR,并促进自噬 (autophagy) 以增加 Aβ 的降解。RSVA405 通过抑制 STAT3 功能具有抗炎作用。RSVA405 也可用于肥胖症的研究。 |
| 溶解性: | DMSO :62 mg/mL (198.48 mM) Ethanol:2 mg/mL (6.4 mM) Water:Insoluble |
| 储备液保存: | -80°C, 6 months -20°C, 1 month |
| 靶点: | AMPK:1 μM (EC50, in cell-based assays) |
| 体外研究: | RSVA405 (0.2-2 μM; 24 h) inhibits adipocyte differentiation. RSVA405 (0.2-2 μM; 24 h) significantly inhibits the expression of peroxisome proliferator-activated receptor (PPAR)-γ, fatty acid synthase (FAS) and fatty acid binding protein 4 (aP2) in 3T3-L1 cells. RSVA405 (1-3 μM; 16 h) inhibits LPS-induced STAT3 activity, intracellular signaling, and cytokine response in activated RAW 264.7 macrophages. RSVA405 (1-3 μM; 24 h) inhibits mTOR, induces autophagy, and facilitates the lysosomal degradation of Aβ, with an EC50 of ∼1 μM in APP-HEK293 cells. |
| 体内研究: | RSVA405 (3 mg/kg; i.p.) attenuates renal injury and protects renal function after ischemia-reperfusion (I/R) in rats. RSVA405 (20-100 mg/kg/d; p.o. for 11 weeks) significantly reduces the body weight gain of mice fed a high-fat diet. |
| 保存条件: | -20°C |
| 注意事项: | 1、为了您的安全和健康,请穿实验服并戴一次性手套操作。 2、以上信息仅做参考交流之用。 |
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