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别名 MSC-2032964A, MSC2032964A
MSC 2032964A 是一种有效的选择性 ASK1 抑制剂 (IC50 = 93 nM),具有口服生物利用度和脑渗透性。它在小鼠 EAE 模型中抑制神经炎症,并在培养的小鼠星形胶质细胞中阻断 LPS 诱导的 ASK1 和 p38 磷酸化。


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MSC 2032964A 是一种有效的选择性 ASK1 抑制剂 (IC50 = 93 nM),具有口服生物利用度和脑渗透性。它在小鼠 EAE 模型中抑制神经炎症,并在培养的小鼠星形胶质细胞中阻断 LPS 诱导的 ASK1 和 p38 磷酸化。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 1 mg | ¥ 666 | In stock | |
| 2 mg | ¥ 883 | In stock | |
| 5 mg | ¥ 1,350 | In stock | |
| 10 mg | ¥ 2,170 | In stock | |
| 25 mg | ¥ 3,520 | In stock | |
| 50 mg | ¥ 4,890 | In stock | |
| 100 mg | ¥ 6,530 | In stock | |
| 200 mg | ¥ 8,790 | In stock |
MSC 2032964A 相关产品
| 产品描述 | MSC 2032964A is a potent selective ASK1 inhibitor (IC50 = 93 nM) that is oral bioavailable and brain permeable. It inhibited neuroinflammation in mouse EAE models and blocked LPS-induced phosphorylation of ASK1 and p38 in cultured mouse astrocytes. |
| 靶点活性 | ASK1:93 nM |
| 别名 | MSC-2032964A, MSC2032964A |
| 分子量 | 362.31 |
| 分子式 | C16H13F3N6O |
| CAS No. | 1124381-43-6 |
| Smiles | FC(F)(F)c1cc(NC2CC2)n2nc(NC(=O)c3cccnc3)nc2c1 |
| 密度 | 1.63 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: 3.62 mg/mL (10 mM), Sonication is recommended. | ||||||||||||||||||||
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DMSO
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