| 生物活性 | |||
|---|---|---|---|
| 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 | |||
|---|---|---|---|
| 1mg | 5mg | 10mg | |
|
1 mM 5 mM 10 mM |
4.13mL 0.83mL 0.41mL |
20.63mL 4.13mL 2.06mL |
41.26mL 8.25mL 4.13mL |
| 参考文献 |
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