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别名 去氢硝苯地平, BAY-b 4759
Dehydro Nifedipine (BAY-b 4759) 是人血浆中硝苯地平的主要代谢物。Dehydro Nifedipine 抑制PC-12细胞葡萄糖摄取,IC50值为130 μM,硝苯地平是一种钙通道阻滞剂,用于治疗高血压和心绞痛。当硝苯地平被细胞色素P450 (CYP)异构体CYP3A4和CYP3A5代谢时形成脱氢硝苯地平。


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Dehydro Nifedipine (BAY-b 4759) 是人血浆中硝苯地平的主要代谢物。Dehydro Nifedipine 抑制PC-12细胞葡萄糖摄取,IC50值为130 μM,硝苯地平是一种钙通道阻滞剂,用于治疗高血压和心绞痛。当硝苯地平被细胞色素P450 (CYP)异构体CYP3A4和CYP3A5代谢时形成脱氢硝苯地平。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 1 mg | ¥ 186 | 现货 | |
| 5 mg | ¥ 413 | 现货 | |
| 10 mg | ¥ 662 | 现货 | |
| 25 mg | ¥ 1,320 | 现货 | |
| 50 mg | ¥ 2,090 | 现货 | |
| 100 mg | ¥ 3,360 | 现货 | |
| 200 mg | ¥ 4,780 | 现货 |
Dehydro Nifedipine 相关产品
| 产品描述 | Dehydro Nifedipine (BAY-b 4759) is the main metabolite of nifedipine in human plasma. Dehydro Nifedipine inhibits glucose uptake in PC-12 cells with an IC50 value of 130 μM. Nifedipine is a calcium channel blocker used in the treatment of hypertension and angina. Dehydronifedipine is formed when it is metabolized by cytochrome P450 (CYP) isomers CYP3A4 and CYP3A5. |
| 靶点活性 | Glucose uptake:130 μM |
| 体外活性 | Dehydro nifedipine 在PC-12细胞中抑制葡萄糖吸收,其半抑制浓度(IC50)值为130 μM[1]。 |
| 别名 | 去氢硝苯地平, BAY-b 4759 |
| 分子量 | 344.32 |
| 分子式 | C17H16N2O6 |
| CAS No. | 67035-22-7 |
| Smiles | COC(=O)c1c(C)nc(C)c(C(=O)OC)c1-c1ccccc1[N+]([O-])=O |
| 密度 | 1.284 g/cm3 (Predicted) |
| 颜色 | Yellow |
| 物理性状 | Solid |
| 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 | Ethanol: 2.7 mg/mL (7.84 mM), Sonication is recommended. DMSO: 27 mg/mL (78.42 mM), Sonication is recommended. DMF: 30 mg/mL (87.13 mM), Sonication is recommended. DMSO:PBS (pH 7.2) (1:10): 0.1 mg/mL (0.29 mM), Sonication is recommended. |
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