241800-97-5
中文名称
ZONIPORIDE DIHYDROCHLORIDE
英文名称
ZONIPORIDE DIHYDROCHLORIDE
CAS
241800-97-5
分子式
C17H16N6O.2HCl
分子量
356.81
MOL 文件
241800-97-5.mol
241800-97-5 结构式
基本信息
中文别名
化合物ZONIPORIDE 英文别名
ZONIPORIDE DIHYDROCHLORIDE[1-(quinolin-5-yl)-5-cyclopropyl-1H-pyrazole-4-carbonyl]guanidine hydrochloride
[1-(QUINOLIN-5-YL)-5-CYCLOPROPYL-1H-PYRAZOLE-4-CARBONYL]GUANIDINE DIHYDROCHLORIDE
5-cyclopropyl-N-(diaminomethylidene)-1-quinolin-5-ylpyrazole-4-carboxamide:hydrochloride
物理化学性质
储存条件Desiccate at -20°C
溶解度≤1mg/ml in ethanol;10mg/ml in DMSO;10mg/ml in dimethyl formamide
形态结晶固体
稳定性吸湿性
常见问题列表
生物活性
Zoniporide (CP-597396) hydrochloride 是 1 型钠氢交换剂 (NHE-1) 的有效和选择性抑制剂。Zoniporide hydrochloride 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 (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 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. |