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863406-85-3

中文名称 ZONIPORIDE HYDROCHLORIDE HYDRATE
英文名称 Zoniporide hydrochloride hydrate
CAS 863406-85-3
分子式 C17H19ClN6O2
分子量 374.83
MOL 文件 863406-85-3.mol
863406-85-3 结构式 863406-85-3 结构式

基本信息

中文别名
化合物 T13413
英文别名
CP-597396 hydrochloride hydrate

物理化学性质

储存条件-20°C储存
溶解度溶于二甲基亚砜
形态Solid
颜色White to off-white

常见问题列表

生物活性
Zoniporide (CP-597396) hydrochloride hydrate 是 1 型钠氢交换剂 (NHE-1) 的有效和选择性抑制剂。Zoniporide hydrochloride hydrate 抑制人 NHE-1 (IC50=14 nM),与其他 NHE 亚型相比具有大于 150 倍的选择性,并有效抑制离体 NHE-1 依赖性的人血小板溶胀 (IC50=59 nM)。
靶点

IC50: 14 nM (NHE-1)

体内研究

Zoniporide hydrochloride hydrate (0.25-4 mg/kg; i.v.; every hour for 2 hours) elicits a dose-dependent reduction in infarct size (ED 50 =0.45 mg/kg/h) in open chest anesthetized rabbits.
Zoniporide exhibits moderate plasma protein binding, has a t 1/2 of 1.5 hours in monkeys, and has one major active metabolite.
Zoniporide hydrochloride hydrate treatment shows the AUC 0-∞ and t 1/2 are 0.07 μg h/mL and 0.5 hours, respectively.

Animal Model: Rabbit
Dosage: 0.25, 1, 4 mg/kg
Administration: Every hour for 2 hours; intravenous injection
Result: Elicited a significant dose-dependent reduction in infarct size in the anesthetized rabbit. The ED 50 was 0.45 mg/kg/h.
Animal Model: Rat
Dosage: 1 mg/kg
Administration: Intravenous injection(Pharmacokinetic Analysis)
Result: The AUC 0-∞ and t 1/2 were 0.07 μg h/mL and 0.5 hours, respectively.
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