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Nurr1 agonist 9 (Compound 36) 是一种Nurr1激动剂,具有EC50 0.090 µM 和 Kd 0.17 µM 的活性。它能够激活Nurr1同型二聚体 (NurRE,EC50=0.094 µM) 以及Nurr1-RXR异型二聚体 (DR5,EC50=0.165 µM)。在类器官帕金森病模型中,Nurr1 agonist 9 能诱导Nurr1调节的酪氨酸羟化酶 (TH) 表达,而且可以通过人脑内皮细胞屏障。
Nurr1 agonist 9 (Compound 36) 是一种Nurr1激动剂,具有EC50 0.090 µM 和 Kd 0.17 µM 的活性。它能够激活Nurr1同型二聚体 (NurRE,EC50=0.094 µM) 以及Nurr1-RXR异型二聚体 (DR5,EC50=0.165 µM)。在类器官帕金森病模型中,Nurr1 agonist 9 能诱导Nurr1调节的酪氨酸羟化酶 (TH) 表达,而且可以通过人脑内皮细胞屏障。

| 产品描述 | Nurr1 agonist 9 (Compound 36) acts as an agonist for Nurr1, with an EC50 of 0.090 µM and a Kd of 0.17 µM. It activates Nurr1 homodimers (NurRE, EC50 = 0.094 µM) and Nurr1-RXR heterodimers (DR5, EC50 = 0.165 µM). This compound induces the expression of Nurr1-regulated tyrosine hydroxylase (TH) in Parkinson's disease organoid models and can penetrate the human brain endothelial cell barrier. |
| 靶点活性 | Nurr1:0.09 μM (EC50), Nurr1:0.17 μM (Ki) |
| 分子式 | C21H19ClN4O2 |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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