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别名 盐酸苄普地尔, CERM 1978
Bepridil hydrochloride (CERM 1978) 是一种钙通道阻滞剂,还抑制 Na+/Ca2+ 交换(NCX)、钠通道和心脏肌膜 KATP 通道,具有抗心绞痛的作用。

Bepridil hydrochloride (CERM 1978) 是一种钙通道阻滞剂,还抑制 Na+/Ca2+ 交换(NCX)、钠通道和心脏肌膜 KATP 通道,具有抗心绞痛的作用。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 2 mg | ¥ 251 | 现货 | |
| 5 mg | ¥ 417 | 现货 | |
| 10 mg | ¥ 583 | 现货 | |
| 25 mg | ¥ 987 | 现货 | |
| 50 mg | ¥ 1,480 | 现货 | |
| 100 mg | ¥ 2,220 | 现货 | |
| 200 mg | ¥ 3,330 | 现货 | |
| 1 mL x 10 mM (in DMSO) | ¥ 456 | 现货 |
| 产品描述 | Bepridil hydrochloride (CERM 1978) is a calcium channel blocker and also inhibits Na+/Ca2+ exchange (NCX), sodium channels and cardiac sarcolemmal KATP channels. |
| 体外活性 | Bepridil (1-100 microM) inhibited the K(ATP) channel current in a concentration-dependent manner. The IC(50) value of bepridil was estimated to be 10.5 microM for outward K(ATP) channel currents (holding potential, +60 mV) and 6.6 microM for inward K(ATP) channel currents (holding potential, -60 mV). Bepridil (0.1-30 microM) also inhibited K(Na) channel currents measured at the holding potential of -60 mV, in a concentration-dependent manner with an IC(50) value of 2.2 microM [2]. |
| 体内活性 | The predominant effects of Bepridil (cumulative dose = 9.0 mg/kg i.v.) in the conscious rat were reduced coronary vascular resistance and heart rate. Bepridil showed selectivity for the coronary circulation since systemic vascular resistance was not significantly reduced until cumulative i.v. dosage of 21.0 mg/kg was administered [1]. |
| 别名 | 盐酸苄普地尔, CERM 1978 |
| 分子量 | 403 |
| 分子式 | C24H35ClN2O |
| CAS No. | 68099-86-5 |
| Smiles | Cl.CC(C)COCC(CN(Cc1ccccc1)c1ccccc1)N1CCCC1 |
| 密度 | 1.054g/cm3 |
| 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: 130 mg/mL (322.58 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
| 体内实验配方 | 10% DMSO+40% PEG300+5% Tween 80+45% Saline: 4 mg/mL (9.93 mM), Sonication is recommended. 请按顺序添加溶剂,在添加下一种溶剂之前,尽可能使溶液澄清。如有必要,可通过加热、超声、涡旋处理进行溶解。工作液建议现配现用。以上配方仅供参考,体内配方并不是绝对的,请根据不同情况进行调整。 | |||||||||||||||||||||||||||||||||||
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。
对于不同动物的给药剂量换算,您也可以参考 更多