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Gallopamil (Methoxyverapamil) 是一种苯烷基胺钙拮抗剂,以浓度依赖性方式抑制酸分泌 (IC50 = 10.9 μM)。Gallopamil 显示出抗心律失常和血管扩张剂的功效。
Gallopamil (Methoxyverapamil) 是一种苯烷基胺钙拮抗剂,以浓度依赖性方式抑制酸分泌 (IC50 = 10.9 μM)。Gallopamil 显示出抗心律失常和血管扩张剂的功效。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 282 | 现货 | |
5 mg | ¥ 1,230 | 现货 | |
10 mg | ¥ 1,960 | 现货 | |
25 mg | ¥ 3,480 | 现货 | |
50 mg | ¥ 4,900 | 现货 | |
100 mg | ¥ 6,890 | 现货 | |
500 mg | ¥ 13,800 | 现货 | |
1 mL x 10 mM (in DMSO) | ¥ 1,320 | 现货 |
产品描述 | Gallopamil (Methoxyverapamil) inhibits acid secretion in a concentration-dependent manner with an IC50 of 10.9 μM. Gallopamil is a potent antiarrhythmic and vasodilator agent. Gallopamil (Methoxyverapamil), a methoxy derivative of Verapamil, is a phenylalkylamine calcium antagonist. |
体内活性 | Gallopamil(5分钟)显著降低收缩压与舒张压,但对心率无显著影响。Gallopamil(0.2 mg/kg; i.v.)显著减少室性心动过速(VT),并完全预防心室纤颤(VF)[2]。 |
别名 | 戈洛帕米, Methoxyverapamil |
分子量 | 484.63 |
分子式 | C28H40N2O5 |
CAS No. | 16662-47-8 |
Smiles | C(CCCN(CCC1=CC(OC)=C(OC)C=C1)C)(C(C)C)(C#N)C2=CC(OC)=C(OC)C(OC)=C2 |
密度 | 1.068 g/cm3 (Predicted) |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||||||||||||
溶解度信息 | DMSO: 95 mg/mL (196.03 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
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