利喷西平
- CAS号:96449-05-7
- 英文名:Rispenzepine
- 中文名:利喷西平
- CBNumber:CB41402427
- 分子式:C19H20N4O2
- 分子量:336.39
- MOL File:96449-05-7.mol
- 储存条件 :Store at -20°C
- 溶解度 :Soluble in DMSO
利喷西平性质、用途与生产工艺
- 生物活性 Rispenzepine 是一种选择性毒蕈碱受体 (M1 和 M3 受体亚型) 拮抗剂。
-
靶点
M 1 , and M 3 receptor
-
体外研究
The presence of muscarinic autoreceptors in human and guinea pig trachea is investigated by comparing the effects of the muscarinic receptor antagonists Pirenzepine (M 1 ), Methoctramine (M 2 ), 4-DAMP (M 3 ), and Rispenzepine (M 1 /M 3 ) on cholinergic neural contractile responses evoked by electrical field stimulation (EFS) and [ 3 H]ACh release. The M 1 , M 1 /M 3 , or M 3 antagonists inhibit the EFS-evoked cholinergic contractile response in a concentration-dependent manner (4-DAMP > Rispenzepine > Pirenzepine), whereas Methoctramine facilitates this response at low concentrations (<3 μM). In ACh release studies, the M 3 antagonist has no significant effect, whereas Pirenzepine, Methoctramine, and Rispenzepine significantly increase ACh release in guinea pig trachea. Rispenzepine almost completely inhibits cholinergic, contractile responses at 0.3 μM (92.7±6.2% inhibition, n=6, p<0.05; pD 2 value of 7.31±0.15) .
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