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SDZ 220-581 is a potent, orally active and competitive antagonist of NMDA receptor(pKi : 7.7).

SDZ 220-581 is a potent, orally active and competitive antagonist of NMDA receptor(pKi : 7.7).
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 2 mg | ¥ 420 | 5日内发货 | |
| 100 mg | ¥ 7,610 | 8-10周 | |
| 1 mL x 10 mM (in DMSO) | ¥ 1,270 | 5日内发货 |
| 产品描述 | SDZ 220-581 is a potent, orally active and competitive antagonist of NMDA receptor(pKi : 7.7). |
| 靶点活性 | NMDAR:pki: 7.7 |
| 分子量 | 369.74 |
| 分子式 | C16H17ClNO5P |
| CAS No. | 174575-17-8 |
| Smiles | ClC1=C(C2=CC(C[C@@H](C(O)=O)N)=CC(CP(=O)(O)O)=C2)C=CC=C1 |
| 密度 | 1.478g/cm3 |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||
| 溶解度信息 | DMSO: 8.57 mg/mL (23.18 mM), Sonication and heating are recommended. | |||||||||||||||||||||||||
| 体内实验配方 | 10% DMSO+40% PEG300+5% Tween-80+45% Saline: 0.5 mg/mL (1.35 mM), Sonication is recommeded. 请按顺序添加溶剂,在添加下一种溶剂之前,尽可能使溶液澄清。如有必要,可通过加热、超声、涡旋处理进行溶解。工作液建议现配现用。以上配方仅供参考,体内配方并不是绝对的,请根据不同情况进行调整。 | |||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||
DMSO
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以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。
对于不同动物的给药剂量换算,您也可以参考 更多