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SDZ 220-581 (hydrochloride)

    
≥96%

SDZ 220-581 (hydrochloride)

源叶(MedMol)
S83998 一键复制产品信息
179411-93-9
C16H18Cl2NO5P
406.197582
SDZ 220-581 hydrochloride
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S83998-10mg
≥96%

¥1370.00

货期:3-5天 - - - -
S83998-50mg
≥96%

¥3430.00

货期:3-5天 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: SDZ 220-581 hydrochloride is an orally active, potent, competitive NMDA receptor antagonist with pKi value of 7.7
靶点: pKi: 7.7 (NMDA receptor);Others
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.
参考文献: 1. Urwyler S, et al. Biphenyl-derivatives of 2-amino-7-phosphono-heptanoic acid, a novel class of potent competitive N-methyl-D-aspartate receptor antagonists--II. Pharmacological characterization in vivo. Neuropharmacology. 1996 Jun;35(6):655-69. 2. Gilmour G, et al. In vitro characterisation of the novel positive allosteric modulators of the mGlu₅ receptor, LSN2463359 and LSN2814617, and their effects on sleep architecture and operant responding in the rat. Neuropharmacology. 2013 Jan;64:224-39.
溶解性: soluble  in  DMSO
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.462 ml 12.309 ml 24.619 ml
5 mM 0.492 ml 2.462 ml 4.924 ml
10 mM 0.246 ml 1.231 ml 2.462 ml
50 mM 0.049 ml 0.246 ml 0.492 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

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摩尔浓度计算器

质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)

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