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    GSK2578215A 1285515-21-0

    簡(jiǎn)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.

    • 產(chǎn)品型號(hào):abs47027961
    • 廠商性質(zhì):生產(chǎn)廠家
    • 更新時(shí)間:2026-01-09
    • 訪  問(wèn)  量:617

    詳細(xì)介紹

    品牌absinCAS1285515-21-0
    分子式C24H18FN3O2純度>98%
    分子量399.42貨號(hào)abs47027961
    規(guī)格10mg供貨周期現(xiàn)貨
    主要用途is a potent and selective應(yīng)用領(lǐng)域化工,生物產(chǎn)業(yè),農(nóng)林牧漁,制藥/生物制藥,綜合

    GSK2578215A  1285515-21-0

    產(chǎn)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.
    純度
    >98%
    儲(chǔ)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
    別名
    LRRK2-kinase inhibitor
    外觀
    white to beige powder
    可溶性/溶解性
    DMSO : 50 mg/mL (125.18 mM)
    生物活性
    靶點(diǎn)
    LRRK2 (G2019S),LRRK2 (WT)
    In vitro(體外研究)
    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(體內(nèi)研究)
    In vivo, GSK2578215A (100 mg/kg i.p.) inhibits Ser910 and Ser935 phosphorylation in mouse spleen and kidney, but not in brain.
    參考文獻(xiàn)
    參考文獻(xiàn)
    研究領(lǐng)域
    研究領(lǐng)域
    NeuroscienceDiseases
    NeuroscienceNeurology processNeurodegenerative diseaseParkinson's diseaseSynuclein
    Drug DiscoverySmall Molecule DrugLead Compound Discovery
    GSK2578215A  1285515-21-0溫馨提示:本產(chǎn)品僅作科研實(shí)驗(yàn)使用,不支持臨床等研究

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