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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。
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 | ¥ 377 | 现货 | |
5 mg | ¥ 943 | 现货 | |
10 mg | ¥ 1,415 | 现货 | |
50 mg | ¥ 3,538 | 现货 |
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 | BAY-b 4759, 去氢硝苯地平 |
分子量 | 344.32 |
分子式 | C17H16N2O6 |
CAS No. | 67035-22-7 |
存储 | store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||||||||||||
溶解度信息 | Ethanol: 2.7 mg/mL (7.8 mM) DMSO: 27.0 mg/mL (78.5 mM) DMF: 30 mg/mL DMSO:PBS (pH 7.2) (1:10): 0.1 mg/mL | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
Ethanol/DMSO
DMSO
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