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79700-61-1

中文名称 多普吡地
英文名称 Dopropidil
CAS 79700-61-1
分子式 C20H35NO2
分子量 321.5
MOL 文件 79700-61-1.mol
79700-61-1 结构式 79700-61-1 结构式

基本信息

中文别名
多普吡地
英文别名
4205CERM
Dopropidil
Pyrrolidine, 1-[1-[(2-methylpropoxy)methyl]-2-[[1-(1-propyn-1-yl)cyclohexyl]oxy]ethyl]-

物理化学性质

储存条件-20°C储存
溶解度溶于二甲基亚砜

安全数据

危险性符号(GHS)GHS hazard pictograms
GHS07
警示词警告
危险性描述H302-H315-H319-H335

常见问题列表

生物活性
Dopropidil 是一种新型的抗心绞痛钙离子调节剂,具有细胞内钙拮抗剂活性,在动物模型中具有抗缺血活性作用。
靶点

Calcium

体外研究

Dopropidil is able to inhibit caffeine-induced contractions of rabbit renal arteries in a calcium-free medium (IC 50 =30.0 uM). Dopropidil inhibits norepinephnne (NE)-induced responses with IC 50 s of 2.7 and 29.8 uM, respectively. At 3 and 10 μM, Dopropidil significantly reduces the maximum increase in diastolic tension evoked by veratrine (IC 50 =2.8 μM).

体内研究

Dopropidil (1 and 2.5 mg/kg) dose-dependently reduces the electrical (ST segment elevation), biochemical (lactate production and potassium release), and mechanical (loss in myocardial segment contractility) perturbations induced by ischemia in the anesthetized dog. Intraduodenal administration of Dopropidil (50 mg/kg) significantly reduces isoproterenol-induced tachycardia. This effect is manifest at 15-120 min following administration of the compound which indicates a rapid absorption and a long duration of action. In conscious dogs Dopropidil (12-14 mg/kg p.o.) reduces resting heart rate by approximately10 beats/min.

"79700-61-1" 相关产品信息
78-27-3 697-37-0