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产品名称 | NMDA receptor ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Empirical Formula | ✔ | 97% | |||||||||||||||||
Dizocilpine maleate |
+++
NMDA receptor, Kd: 37.2 nM |
99%+ | |||||||||||||||||
Felbamate |
+
NMDAR, IC50: 1.8 mM |
98% | |||||||||||||||||
(-)-Dizocilpine maleate |
++++
NMDA receptor, Ki: 30.5 nM |
98% | |||||||||||||||||
Ifenprodil tartrate |
+++
NMDA Receptor, IC50: 0.3 μM |
98% | |||||||||||||||||
Spermidine | ✔ | Autophagy | 98% GC | ||||||||||||||||
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 |
描述 | Traxoprodil mesylate (CP101,606) is a potent and selective NMDA antagonist and protect hippocampal neurons with an IC50 of 10 nM. Traxoprodil is effective at 1 mg/kg to block NMDA (ip) stimulated cfos induction in mice[1]. Traxoprodil (20nmol i.c.v.) increased the latency to generalized tonic-clonic seizures induced by PTZ (pentylenetetrazol) (70mg/kg; i.p.). Traxoprodil (60mg/kg, p.o.) increased the latency to clonic and generalized seizures, and decreased the total time spent in seizures[2]. Traxoprodil at a dose of 20 and 40 mg/kg exhibited antidepressant activity in the FST (forced swim test) and it was not related to changes in animals' locomotor activity[3]. |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
2.09mL 0.42mL 0.21mL |
10.47mL 2.09mL 1.05mL |
20.94mL 4.19mL 2.09mL |
CAS号 | 189894-57-3 |
分子式 | C21H35NO9S |
分子量 | 477.57 |
SMILES Code | CS(=O)(O)=O.[H]O[H].[H]O[H].[H]O[H].C[C@H](N1CCC(C2=CC=CC=C2)(O)CC1)[C@@H](O)C3=CC=C(O)C=C3 |
MDL No. | MFCD22377951 |
别名 | |
运输 | 蓝冰 |
InChI Key | LUILKELNVBKKTG-ZOZJKLBQSA-N |
Pubchem ID | 9826324 |
存储条件 |
In solvent -20°C:3-6个月-80°C:12个月 Pure form Inert atmosphere, 2-8°C |