生物活性 | |||
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描述 | Rislenemdaz, also known as CERC-301, inhibits calcium influx agonist-stimulated NMDA-GluN1a/GluN2B L(tk-) cells with an IC50 of 3.6 nM. Rislenemdaz is at least 1000-fold more selective for the GluN2B receptor compared to all targets tested, including hERG potassium channels. At 10 uM, Rislenemdaz is also minimally active against sigma-type receptors[1]. |
实验方案 | |||
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1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
2.79mL 0.56mL 0.28mL |
13.95mL 2.79mL 1.40mL |
27.90mL 5.58mL 2.79mL |
参考文献 |
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