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Verapamil hydrochloride (Verapamil HCl) 是一种钙通道阻滞剂,是一种可口服的 P 糖蛋白 (P-gp) 抑制剂,可抑制CYP3A4,用于高血压、心律不齐和心绞痛的研究。
Verapamil hydrochloride (Verapamil HCl) 是一种钙通道阻滞剂,是一种可口服的 P 糖蛋白 (P-gp) 抑制剂,可抑制CYP3A4,用于高血压、心律不齐和心绞痛的研究。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
500 mg | ¥ 339 | 现货 | |
1 g | ¥ 434 | 现货 | |
1 mL x 10 mM (in DMSO) | ¥ 417 | 现货 |
产品描述 | Verapamil hydrochloride (Verapamil HCl) is a calcium channel blocker that is a class IV anti-arrhythmia agent. |
体外活性 | Verapamil可以抗心律失常,减少大鼠心脏氧的消耗,并保存Cx43蛋白. |
体内活性 | Verapamil和Diltiazem能够基本上抑制重组CES2的水解酶活性(Ki分别为0.25 ± 0.02、3.84 ± 0.99 μM)。 |
细胞实验 | Verapamil is dissolved in DMSO and stored, and then diluted with appropriate media before use[1]. Cells (1×105) are treated with 10 nM Bortezomib and/or 70 μM Verapamil for 16 hours and incubated for another 4 hours with Alamar-Blue. Activity of the mitochondrial dehydrogenase results in conversion of the coloring, which is followed by measurement of the absorption using a spectrophotometer[1]. |
别名 | Manidon, (±)-Verapamil hydrochlorid, Verapamil HCl, Calcan hydrochloride, 盐酸维拉帕米 |
分子量 | 491.06 |
分子式 | C27H39ClN2O4 |
CAS No. | 152-11-4 |
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: 50 mg/mL (101.82 mM) H2O: 24.6 mg/mL (50 mM) | ||||||||||||||||||||||||||||||||||||||||
溶液配制表 | |||||||||||||||||||||||||||||||||||||||||
H2O/DMSO
DMSO
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