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产品名称 | AMPK ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
WZ4003 |
++++
NUAK1, IC50: 20 nM NUAK2, IC50: 100 nM |
98+% | |||||||||||||||||
Dorsomorphin |
++
AMPK, Ki: 109 nM |
99% | |||||||||||||||||
HTH-01-015 |
+++
NUAK1 , IC50: 100 nM |
99%+ | |||||||||||||||||
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 |
描述 | RSVA405 is a potent orally active activator of AMPK with an EC50 value of 1 μM.RSVA405 promotes CaMKKβ-dependent activation of AMPK, inhibits mTOR, and facilitates autophagy to increase Aβ degradation.RSVA405 has anti-inflammatory effects through inhibition of STAT3.RSVA405 has been used in the study of obesity[1][2][3][4]. In the concentration range of 0.2-2 μM for 24 hours, RSVA405 inhibited adipocyte differentiation and significantly suppressed the expression of PPARγ, FAS and aP2 in 3T3-L1 cells[2].In the concentration range of 1-3 μM for 16 hours, RSVA405 inhibited LPS-induced STAT3 activity, intracellular signalling and cytokine responses in activated RAW 264.7 macrophages[3] .In the concentration range of 1-3 μM, acting for 24 hours, RSVA405 inhibited mTOR, induced autophagy, promoted lysosomal degradation of Aβ, and had an EC50 value of 1 μM in APP-HEK293 cells[4] . |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
3.20mL 0.64mL 0.32mL |
16.01mL 3.20mL 1.60mL |
32.01mL 6.40mL 3.20mL |
CAS号 | 140405-36-3 |
分子式 | C17H20N4O2 |
分子量 | 312.37 |
SMILES Code | O=C(C1=CC=NC=C1)N/N=C/C2=CC=C(N(CC)CC)C=C2O |
MDL No. | MFCD00542031 |
别名 | |
运输 | 蓝冰 |
存储条件 |
In solvent -20°C:3-6个月-80°C:12个月 Pure form Sealed in dry, 2-8°C |