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GSK-626616 是一种口服具有活力的 DYRK3抑制剂 (IC50:0.7 nM)。它以相似的效力抑制 DYRK 家族的其他成员,可用于研究贫血。


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GSK-626616 是一种口服具有活力的 DYRK3抑制剂 (IC50:0.7 nM)。它以相似的效力抑制 DYRK 家族的其他成员,可用于研究贫血。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 1 mg | ¥ 357 | In stock | |
| 5 mg | ¥ 933 | In stock | |
| 10 mg | ¥ 1,570 | In stock | |
| 25 mg | ¥ 2,660 | In stock | |
| 50 mg | ¥ 3,890 | In stock | |
| 100 mg | ¥ 5,550 | In stock | |
| 200 mg | ¥ 7,550 | In stock | |
| 1 mL x 10 mM (in DMSO) | ¥ 1,090 | In stock |
GSK-626616 相关产品
| 产品描述 | GSK-626616 is a potent and orally bioavailable DYRK3 inhibitor (IC50: 0.7 nM). It inhibits other members of the DYRK family with similar potency. GSK-626616 is a potential therapy for the treatment of anemia. |
| 靶点活性 | β-glucuronidase:0.7 nM |
| 体外活性 | GSK-626616 (serum-deprived HeLa cells) reduces EGF-induced phosphorylation of PRAS40 at Thr246. GSK-626616 enhances the binding of PRAS40 to mTORC1[2]. GSK-626616 abolishes the phosphorylation of S6K1 at Thr389 in nonstimulated HeLa cells. GSK-626616 reduces the phosphorylation of S6K1 at Thr389 in EGF- and insulin-stimulated HeLa cells, showing that mTORC1 activity is impaired[2]. |
| 分子量 | 401.27 |
| 分子式 | C18H10Cl2N4OS |
| CAS No. | 1025821-33-3 |
| Smiles | Clc1cccc(Cl)c1NC1=NC(=O)\C(S1)=C\c1ccc2nccnc2c1 |
| 密度 | 1.55 g/cm3 (Predicted) |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| 溶解度信息 | DMSO: 49 mg/mL (122.11 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
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