产品
编 号：F209356
分子式：C16H17ClNO5P
分子量：369.74
分子式：C16H17ClNO5P
分子量：369.74
产品类型
规格
价格
是否有货
10mM*1mL in DMSO
询价
询价
5mg
询价
询价
10mg
询价
询价
50mg
询价
询价
结构图
CAS No: 174575-17-8
产品详情
生物活性：
SDZ 220-581 is an orally active, potent, competitive NMDA receptor antagonist with pKi value of 7.7.
体内研究：
SDZ 220-581 (3.2-32 mg/kg; oral administration; for 24 hours; male OF-l mice) treatment dose-dependently protects mice against maximal electroshock seizures (MES). The time-course of protection by SDZ 220-581 is characterized by a rapid onset and long duration of action.Animal Model:Male OF-l mice (18-26 g)
Dosage:3.2 mg/kg, 10 mg/kg, 32 mg/kg
Administration:Oral administration; for 24 hours
Result:Dose-dependently protected mice against maximal electroshock seizures (MES) upon oral administration.
SDZ 220-581 is an orally active, potent, competitive NMDA receptor antagonist with pKi value of 7.7.
体内研究：
SDZ 220-581 (3.2-32 mg/kg; oral administration; for 24 hours; male OF-l mice) treatment dose-dependently protects mice against maximal electroshock seizures (MES). The time-course of protection by SDZ 220-581 is characterized by a rapid onset and long duration of action.Animal Model:Male OF-l mice (18-26 g)
Dosage:3.2 mg/kg, 10 mg/kg, 32 mg/kg
Administration:Oral administration; for 24 hours
Result:Dose-dependently protected mice against maximal electroshock seizures (MES) upon oral administration.
产品资料
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