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LY3214996研究進(jìn)展

發(fā)布日期:2017-10-30   瀏覽次數(shù):0
核心提示:a href=https://www.medchemexpress.com/LY3214996.htmlLY3214996/a產(chǎn)品描述:LY3214996 is a highly selective inhibitor of bE
<a href="https://www.medchemexpress.com/LY3214996.html">LY3214996</a>產(chǎn)品描述:LY3214996 is a highly selective inhibitor of <b>ERK1</b> and <b>ERK2</b>, with <b>IC<sub>50</sub></b> of 5 nM for both enzymes in biochemical assays.

IC50 & Target: IC50: 5 nM (ERK1/2)<sup>[1]</sup>

<i><b>In Vitro:</b></i> LY3214996 is a highly selective inhibitor of ERK1 and ERK2, with IC<sub>50</sub> of 5 nM for both enzymes in biochemical assays. LY3214996 potently inhibits cellular phospho-RSK1 in BRAF and RAS mutant cancer cell lines. In an unbiased tumor cell panel sensitivity profiling for inhibition of cell proliferation, tumor cells with MAPK pathway alterations including BRAF, NRAS or KRAS mutation are generally sensitivity to LY3214996<sup>[1]</sup>.

<i><b>In Vivo:</b></i> In tumor xenograft models, LY3214996 inhibits PD biomarker phospho-p90RSK1 in tumors and the PD effects are correlated with compound exposures and anti-tumor activities. LY3214996 shows either similar or superior anti-tumor activity as compared to other published ERK inhibitors in BRAF or RAS mutant c<br><br>
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已為全球多個(gè)知名企業(yè)、院校構(gòu)建各種定制型化合物庫。</span><br><br>產(chǎn)品鏈接:<a href="http://www.medchemexpress.cn/ly3214996.html">www.medchemexpress.cn/ly3214996.html</a><br><br></span><img style="width: 600.0px;height: 310.0px;"

src="http://img.dxycdn.com/trademd/upload/userfiles/image/2014/08/A1408605159png_small.jpg"

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