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GW806742X 是ATP 模拟物,是MLKL 抑制剂,可结合 MLKL 假激酶结构域,Kd 值为 9.3μM。它对VEGFR2的IC50为 2 nM,延缓 MLKL 膜移位并抑制坏死。


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GW806742X 是ATP 模拟物,是MLKL 抑制剂,可结合 MLKL 假激酶结构域,Kd 值为 9.3μM。它对VEGFR2的IC50为 2 nM,延缓 MLKL 膜移位并抑制坏死。
| 规格 | 价格 | 库存 | 数量 | 
|---|---|---|---|
| 2 mg | ¥ 258  | In stock | |
| 5 mg | ¥ 413  | In stock | |
| 10 mg | ¥ 647  | In stock | |
| 25 mg | ¥ 1,190  | In stock | |
| 50 mg | ¥ 1,990  | In stock | |
| 100 mg | ¥ 3,120  | In stock | |
| 1 mL x 10 mM (in DMSO) | ¥ 523  | In stock | 
GW806742X 相关产品
| 产品描述 | GW806742X is an inhibitor of Mixed Lineage Kinase Domain-Like protein (MLKL) which binds the MLKL pseudokinase domain (Kd: 9.3 μM) with anti-necroptosis activity. GW806742X has activity against VEGFR2.  | 
| 靶点活性 |  MLKL:9.3 μM (Kd), VEGFR2:2 nM  | 
| 体外活性 | GW806742X (1 μM) 抑制 MLKL 转移到膜上。在1 ng/mL TNF作用下,GW806742X (0.1-10000 nM) 可以使50%的野生型鼠皮肤成纤维细胞(MDFs)免受TSQ诱导的坏死性死亡,其半抑制浓度(IC50)< 50 nM。  | 
| 分子量 | 573.55 | 
| 分子式 | C25H22F3N7O4S | 
| CAS No. | 579515-63-2 | 
| Smiles | CN(c1ccc(NC(=O)Nc2ccc(OC(F)(F)F)cc2)cc1)c1ccnc(Nc2cccc(c2)S(N)(=O)=O)n1 | 
| 密度 | 1.524 g/cm3 (Predicted) | 
| 颜色 | White | 
| 物理性状 | Solid | 
| 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: 125 mg/mL (217.94 mM), Sonication is recommended.   | |||||||||||||||||||||||||||||||||||
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