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CK2α-IN-1 是一种选择性非 ATP 竞争的 CK2α 抑制剂 ,IC50 为 7.0 µM, Ki 为 1.6 µM。CK2α-IN-1 具有潜在的抗癌活性,可用于研究癌症。


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CK2α-IN-1 是一种选择性非 ATP 竞争的 CK2α 抑制剂 ,IC50 为 7.0 µM, Ki 为 1.6 µM。CK2α-IN-1 具有潜在的抗癌活性,可用于研究癌症。
| 规格 | 价格 | 库存 | 数量 | 
|---|---|---|---|
| 1 mg | ¥ 148  | In stock | |
| 5 mg | ¥ 333  | In stock | |
| 10 mg | ¥ 493  | In stock | |
| 25 mg | ¥ 822  | In stock | |
| 50 mg | ¥ 1,180  | In stock | |
| 100 mg | ¥ 1,780  | In stock | |
| 200 mg | ¥ 2,630  | In stock | 
CK2α-IN-1 相关产品
| 产品描述 | CK2α-IN-1 is a selective non-ATP-competitive CK2α inhibitor with an IC50 of 7.0 µM and a Ki of 1.6 µM.CK2α-IN-1 exhibits potential anticancer activity and can be used in cancer research.  | 
| 靶点活性 |  CK2α:7.0 µM  | 
| 分子量 | 341.34 | 
| 分子式 | C16H11N3O4S | 
| CAS No. | 443747-52-2 | 
| Smiles | N(C1=NC(=CS1)C2=CC(N(=O)=O)=CC=C2)C3=CC(C(O)=O)=CC=C3 | 
| 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: 55 mg/mL (161.13 mM), Sonication is recommended.   | |||||||||||||||||||||||||||||||||||
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DMSO 
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