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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 | ¥ 428 | In stock | |
5 mg | ¥ 931 | In stock | |
10 mg | ¥ 1,690 | 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) | ¥ 1,730 | 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 |
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. | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
DMSO
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以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。
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