1. Autophagy
  2. LRRK2
  3. Lu AF58786

Lu AF58786 是一种高效且选择性的 LRRK2 抑制剂,IC50 值为 12 nM。Lu AF58786 对 LRRK2 G2019S 和 LRRK2 A2016T 也具有抑制活性,IC50 值分别为 19 nM 和 93 nM。Lu AF58786 可抑制人外周血单核细胞中 LRRK2、Rab10 和 Rab12 的磷酸化。Lu AF58786 可用于帕金森病的研究。

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Lu AF58786

Lu AF58786 Chemical Structure

CAS No. : 1632368-13-8

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  • 生物活性

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生物活性

Lu AF58786 is a potent and selective LRRK2 inhibitor with an IC50 of 12 nM. Lu AF58786 also exhibits inhibition activity against LRRK2 G2019S and LRRK2 A2016T with IC50s of 19 and 93 nM. Lu AF58786 inhibits phosphorylation of LRRK2, Rab10 and Rab12 in human peripheral blood mononuclear cells. Lu AF58786 can be used for parkinson’s disease research[1][2].

分子量

328.37

Formula

C19H16N6

CAS 号
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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产品名称:
Lu AF58786
目录号:
HY-180320
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