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SM-6586 是一种有效的钙离子通道拮抗剂,对 Na+/H+ 和 Na+/Ca2+ 交换通道有抑制作用,可用于研究脑血管疾病和高血压等疾病。
SM-6586 是一种有效的钙离子通道拮抗剂,对 Na+/H+ 和 Na+/Ca2+ 交换通道有抑制作用,可用于研究脑血管疾病和高血压等疾病。

| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 1 mg | ¥ 4,900 | 现货 | |
| 5 mg | ¥ 12,600 | 现货 |
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| 产品描述 | SM-6586 is a potent calcium channel antagonist with inhibitory effects on Na+/H+ and Na+/Ca2+ exchange channels, and can be used in the study of cerebrovascular disease and hypertension, among other diseases. |
| 体内活性 | In spontaneously hypertensive rats treated with SM-6586, the survival rate after bilateral common carotid artery ligation is higher, the brain water content is lower, and the ATP level is higher, while lactate level is decreased. In focal ischemia models, the SM-treated group shows a reduction of T1 relaxation time. Additionally, the brain water content is significantly decreased in the SM-treated group[1]. |
| 分子量 | 489.52 |
| 分子式 | C26H27N5O5 |
| CAS No. | 103898-38-0 |
| Smiles | O=C(C1=C(C)NC(C)=C(C1C2=CC([N+]([O-])=O)=CC=C2)C3=NC(CN(CC4=CC=CC=C4)C)=NO3)OC |
| 密度 | 1.31g/cm3 |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. 实际储存温度请以COA为准 |
对于不同动物的给药剂量换算,您也可以参考 更多