生物活性 | |||
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描述 | GPR52 antagonist-1 is a GPR52 antagonist with an IC50 of 0.63 μM, which reduces mutant huntingtin protein (mHTT) levels by targeting GPR52 and enhances the survival of mouse primary striatal neurons[1]. |
实验方案 | |||
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1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
4.13mL 0.83mL 0.41mL |
20.63mL 4.13mL 2.06mL |
41.27mL 8.25mL 4.13mL |
参考文献 |
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