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PF-06456384 trihydrochloride是一种高效和选择性 NaV1.7 抑制剂(IC50 =0.01 nM),通过蛋白质配体结合而不是抑制相关的钠通道发挥作用,专为静脉输注设计且可用于疼痛研究。

PF-06456384 trihydrochloride是一种高效和选择性 NaV1.7 抑制剂(IC50 =0.01 nM),通过蛋白质配体结合而不是抑制相关的钠通道发挥作用,专为静脉输注设计且可用于疼痛研究。
| 规格 | 价格 | 库存 | 数量 | 
|---|---|---|---|
| 1 mg | ¥ 347  | In stock | |
| 5 mg | ¥ 828  | In stock | |
| 10 mg | ¥ 1,490  | In stock | |
| 25 mg | ¥ 2,990  | In stock | |
| 50 mg | ¥ 4,290  | In stock | |
| 100 mg | ¥ 6,030  | In stock | |
| 1 mL x 10 mM (in DMSO) | ¥ 1,350  | In stock | 
PF-06456384 trihydrochloride 相关产品
| 产品描述 | PF-06456384 trihydrochloride is a highly efficient and selective NaV1.7 inhibitor (IC50 = 0.01 nM), acting through protein-ligand binding rather than inhibiting the associated sodium channel. It is specifically designed for intravenous infusion and can be used in pain research.  | 
| 靶点活性 |  NaV1.7:0.01 nM  | 
| 别名 | PF-06456384 三盐酸盐, PF06456384 trihydrochloride | 
| 分子量 | 829.18 | 
| 分子式 | C35H35Cl3F3N7O3S2 | 
| CAS No. | 1834610-75-1 | 
| Smiles | N#CC1=CC(S(=O)(NC2=NC=NS2)=O)=CC=C1OC3=CC=C(C4=CC(C(F)(F)F)=CC=C4)C=C3C5=CC(CNCCC6CCNCC6)=NC=C5.Cl.Cl.Cl | 
| 颜色 | White | 
| 物理性状 | Solid | 
| 存储 | store at low temperature | 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: 100 mg/mL (120.6 mM), Sonication is recommended.   | |||||||||||||||||||||||||||||||||||
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