中文名 | 盐酸去甲维拉帕米 |
英文名 | Nor Verapamil Hydrochloride |
别名 | 去甲维拉帕米 维拉帕米杂质J 盐酸去甲维拉帕米 盐酸去甲维他帕米 去甲维拉帕米盐酸盐 N-去甲维拉帕米盐酸盐 维拉帕米杂质J (EP) 盐酸去甲维拉帕米(N-去甲 盐酸维拉帕米) |
英文别名 | NORVERAPAMIL HCL NORVERAPAMIL HYDROCHLORIDE Nor Verapamil Hydrochloride n-nor-(±)-verapamil hydrochloride (+-)-VERAPAMIL HYDROCHLORIDE, NOR-METHYL (NORVERAPAMIL HYDROCH a-[3-[[2-(3,4-Dimethoxyphenyl)ethyl]amino]propyl]-3,4-dimethoxy-a-(1-methylethyl)-benzeneacetonitril a-[3-[[2-(3,4-Dimethoxyphenyl)ethyl]amino]propyl]-3,4-dimethoxy-a-(1-methylethyl)-benzeneacetonitrile α-[3-[[2-(3,4-Dimethoxyphenyl)ethyl]amino]propyl]-3,4-dimethoxy-α-(1-methylethyl)- benzeneacetonitrile |
CAS | 67812-42-4 |
化学式 | C26H37ClN2O4 |
分子量 | 477.04 |
熔点 | softens at 50°C, 155-160°C dec. |
闪点 | 9℃ |
溶解度 | H2O: >10 mg/mL |
存储条件 | desiccated |
稳定性 | 吸湿性 |
外观 | 固体 |
颜色 | white |
体外研究 | Norverapamil hydrochloride ((±)-Norverapamil hydrochloride) is similarly effective as verapamil at inhibiting isoniazid and rifampicin tolerance and killing of intracellular M. tuberculosis in the absence of other drugs. norverapamil, also inhibits macrophage-induced tolerance and achieves similar serum levels to verapamil. Verapamil and its major metabolite norverapamil were identified to be both mechanism-based inhibitors and substrates of CYP3A and reported to have non-linear pharmacokinetics in clinic. |
危险品运输编号 | UN 2811 6.1/PG 3 |
WGK Germany | 3 |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 2.096 ml | 10.481 ml | 20.963 ml |
5 mM | 0.419 ml | 2.096 ml | 4.193 ml |
10 mM | 0.21 ml | 1.048 ml | 2.096 ml |
5 mM | 0.042 ml | 0.21 ml | 0.419 ml |
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