生物活性 | |||
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描述 | CP21R7 is a selective GSK-3β inhibitor, exhibiting an IC50 of 1.8 nM; in contrast, its IC50 against PKCα is 1900 nM[1]. When used at a concentration of 3 μM, CP21R7 robustly activates the canonical Wnt signaling pathway to its highest level. It also significantly boosts the total intracellular levels of β-catenin. Moreover, when combined with BMP4, CP21R7 prompts the differentiation of human pluripotent stem cells (hPSCs) into mesoderm[2]. | ||
作用机制 | CP21R7 may occupy the ATP binding pocket.[1] |
实验方案 | |||
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1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
3.15mL 0.63mL 0.32mL |
15.76mL 3.15mL 1.58mL |
31.51mL 6.30mL 3.15mL |
参考文献 |
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