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JW 55研究進(jìn)展

發(fā)布日期:2017-11-02   瀏覽次數(shù):0
核心提示:a href=https://www.medchemexpress.com/JW-55.htmlJW 55/a產(chǎn)品描述:JW 55 is a potent and selective b-catenin/b signaling p
JW 55產(chǎn)品描述:JW 55 is a potent and selective β-catenin signaling pathway inhibitor, which functions via inhibition of the PARP domain of tankyrase 1 and tankyrase 2 (TNKS1/2). JW 55 decreases auto-PARsylation of TNKS1/2 in vitro with IC50s of 1.9 μM and 830 nM respectively. IC50 & Target: IC50: 1.9 μM (TNKS1); 830 nM (TNKS2)[1]In Vitro: JW 55 (JW55) is a potent and selective inhibitor of the canonical Wnt pathway. Wnt3a-induced HEK293 cells containing a transiently transfected ST-Luc (SuperTop-luciferase) reporter show inhibition by JW55 with an IC50 value of 470 nM. JW55 is effective in the range of 1 to 5 μM in SW480 cells and 0.01 to 5 μM in HCT-15 cells. JW55 is effective in the range of 1 to 5 μM in SW480 cells and 0.01 to 5 μM in HCT-15 cells[1]. In Vivo: JW 55 (100 mg/kg, orally) reduces tumor development in conditional Apc knockout mice. JW55 reduces XWnt8-induced axis duplication inXenop


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