生物活性 | |||
---|---|---|---|
靶点 |
|
||
描述 | Indirubin-3′-oxime (IDR3O), a synthetic derivative of indirubin, strongly inhibits cyclin-dependent kinases (CDKs) and glycogen synthase kinase 3β (GSK3β). It also directly inhibits all three JNK isoforms (JNK1, JNK2, JNK3), with IC50 values of 0.8 μM, 1.4 μM, and 1.0 μM, respectively, and activates Wnt/β-catenin signaling in chondrocytes to promote height growth [1][2][3]. |
实验方案 | |||
---|---|---|---|
1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
3.61mL 0.72mL 0.36mL |
18.03mL 3.61mL 1.80mL |
36.07mL 7.21mL 3.61mL |
参考文献 |
---|