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GSK2578215A 1285515-21-0

简要描述:GSK2578215A 1285515-21-0
GSK2578215A is a potent and selective LRRK2 kinase inhibitor with IC50 of 8.9 nM and 10.9 nM for LRRK2 (G2019S) and LRRK2 (WT), respectively.

  • 产品型号:abs47027961
  • 厂商性质:生产厂家
  • 更新时间:2026-01-09
  • 访  问  量:633

详细介绍

品牌absinCAS1285515-21-0
分子式C24H18FN3O2纯度>98%
分子量399.42货号abs47027961
规格10mg供货周期现货
主要用途is a potent and selective应用领域化工,生物产业,农林牧渔,制药/生物制药,综合

GSK2578215A  1285515-21-0

产品描述
描述
GSK2578215A is a potent and selective LRRK2 kinase inhibitor with IC50 of 8.9 nM and 10.9 nM for LRRK2 (G2019S) and LRRK2 (WT), respectively.
纯度
>98%
储存/保存方法
Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.
基本信息
别名
LRRK2-kinase inhibitor
外观
white to beige powder
可溶性/溶解性
DMSO : 50 mg/mL (125.18 mM)
生物活性
靶点
LRRK2 (G2019S),LRRK2 (WT)
In vitro(体外研究)
GSK2578215A induces a dose-dependent inhibition of Ser910 and Ser935 phosphorylation in both wild-type LRRK2 and LRRK2 stably transfected into HEK293 cells, and induces similar dose-dependent Ser910 and Ser935 dephosphorylation of endogenous LRRK2 in mouse Swiss 3T3 cells. In SH-SY5Y cells, GSK2578215A impairs the autophagy flux by altering autophagosome–lysosome fusion, and induces mitophagy though induction of Drp-1-mediated mitochondrial fission and mitochondrial-derived ROS signaling.
In vivo(体内研究)
In vivo, GSK2578215A (100 mg/kg i.p.) inhibits Ser910 and Ser935 phosphorylation in mouse spleen and kidney, but not in brain.
参考文献
参考文献
研究领域
研究领域
NeuroscienceDiseases
NeuroscienceNeurology processNeurodegenerative diseaseParkinson's diseaseSynuclein
Drug DiscoverySmall Molecule DrugLead Compound Discovery
GSK2578215A  1285515-21-0温馨提示:本产品仅作科研实验使用,不支持临床等研究

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