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Besipirdine hydrochloride 是一种非受体依赖性拟胆碱化合物,具有α-肾上腺素能活性和心血管活性。Besipirdine hydrochloride 抑制电压依赖性钠钾通道,抑制生物胺的摄取。Besipirdine hydrochloride 可减少大鼠的时间表诱导的烦渴,增强中枢神经系统中的胆碱能和肾上腺素能神经传递。
Besipirdine hydrochloride 是一种非受体依赖性拟胆碱化合物,具有α-肾上腺素能活性和心血管活性。Besipirdine hydrochloride 抑制电压依赖性钠钾通道,抑制生物胺的摄取。Besipirdine hydrochloride 可减少大鼠的时间表诱导的烦渴,增强中枢神经系统中的胆碱能和肾上腺素能神经传递。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 1,300 | 现货 | |
5 mg | ¥ 3,250 | 现货 | |
10 mg | ¥ 4,750 | 现货 | |
25 mg | ¥ 7,480 | 现货 | |
50 mg | ¥ 9,870 | 现货 | |
100 mg | ¥ 13,600 | 现货 |
产品描述 | Besipirdine hydrochloride is a non-receptor-dependent cholinomimetic compound with alpha-adrenergic and cardiovascular activities.Besipirdine hydrochloride inhibits voltage-dependent sodium-potassium channels and inhibits biogenic amine uptake.Besipirdine hydrochloride reduces schedule-induced thirst and enhances cholinergic and adrenergic neurotransmission in the central nervous system in rats. |
别名 | 贝西吡啶盐酸盐, HP 749 hydrochloride, Besipirdine hydrochloride(119257-34-0 Free base) |
分子量 | 287.79 |
分子式 | C16H18ClN3 |
CAS No. | 130953-69-4 |
Smiles | Cl.N=1C=CC(=CC1)N(N2C=CC=3C=CC=CC32)CCC |
密度 | no data available |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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