化学信息:
化学名 | 1-[(8R)-5-(4-aminophenyl)-8-methyl-8,9-dihydro-[1,3]dioxolo[4,5-h][2,3]benzodiazepin-7-yl]ethanone | |
简称 | Talampanel | |
别名 |
LY300164, GYKI-53773, LY-300164, LY 300164, GYKI53773, GYKI 53773 |
|
中文名 | 他仑帕奈 | |
化学式 | C19H19N3O3 | |
分子量 | 337.37 | |
CAS号 | 161832-65-1 | |
纯度 | 98% | |
溶剂/溶解度 |
Water<1mg/ml; DMSO4mg/ml; Ethanol<1mg/ml |
|
溶液配制 | 5mg加入1.48ml DMSO,或者每3.37mg加入1ml DMSO,配制成10mM溶液。SF8997-10mM用DMSO配制。 |
生物信息:
产品描述 | Talampanel is a potent and selective AMPA-receptor antagonist, is a potential new antiepileptic drug (AED). | ||||
信号通路 | Transmembrane Transporters | ||||
靶点 | AMPA | - | - | - | - |
IC50 | - | - | - | - | - |
体外研究 | Talampanel is a glutamate receptor inhibitor with anti-seizure activity. | ||||
体内研究 | Talampanel reduces motoneuronal calcium in a mouse model of ALS, but its effi cacy declines as the disease progresses, suggesting that medication initiation in the earlier stages of the disease might be more effective. | ||||
临床实验 | N/A | ||||
特征 | N/A |
相关实验数据(此数据来自于公开文献,碧云天并不保证其有效性):
酶活性检测实验 | |
方法 | N/A |
细胞实验 | |
细胞系 | N/A |
浓度 | N/A |
处理时间 | N/A |
方法 | N/A |
动物实验 | |
动物模型 | N/A |
配制 | N/A |
剂量 | N/A |
给药方式 | N/A |
产品编号 | 产品名称 | 包装 |
SF8997-10mM | Talampanel (AMPAR拮抗剂) | 10mM×0.2ml |
SF8997-5mg | Talampanel (AMPAR拮抗剂) | 5mg |
SF8997-25mg | Talampanel (AMPAR拮抗剂) | 25mg |
— | 说明书 | 1份 |
保存条件:
-20℃保存,至少一年有效。5mg和25mg包装也可室温保存,至少6个月有效。如果溶于非DMSO溶剂,建议分装后-80℃保存,预计6个月内有效。