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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 | TMPA is characterized as a high-affinity antagonist of Nur77, a mechanism that prompts the liberation and translocation of LKB1 into the cytoplasm, thereby activating AMPKα. This action has significant implications for diabetes management, as TMPA effectively reduces blood glucose levels and mitigates insulin resistance in various models of diabetes, including type II db/db, high-fat diet, and streptozotocin-induced diabetic mice. Furthermore, TMPA demonstrates potential therapeutic value in cancer and T-cell apoptosis regulation by diminishing restimulation-induced cell death (RICD) in human T cells[1][2]. |
Animal study | When administered intraperitoneally at a dose of 50 mg/kg daily for 19 days, TMPA significantly lowers blood glucose and enhances glucose tolerance in type II diabetic mice, showcasing its therapeutic potential for diabetes treatment[1]. |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
2.63mL 0.53mL 0.26mL |
13.14mL 2.63mL 1.31mL |
26.28mL 5.26mL 2.63mL |
CAS号 | 1258275-73-8 |
分子式 | C21H32O6 |
分子量 | 380.48 |
SMILES Code | O=C(OCC)CC1=C(C(CCCCCCC)=O)C=C(OC)C(OC)=C1OC |
别名 | |
运输 | 蓝冰 |
InChI Key | WCYMJQXRLIDSAQ-UHFFFAOYSA-N |
Pubchem ID | 60146245 |
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 |
溶解方案 |
请根据您的动物给药指南选择适当的溶解方案。 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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