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VUF10460研究進展

發(fā)布日期:2017-10-30   瀏覽次數(shù):0
核心提示:a href=https://www.medchemexpress.com/VUF10460.htmlVUF10460/a產(chǎn)品描述:VUF10460 is a non-imidazole histamine bH4/b recep
<a href="https://www.medchemexpress.com/VUF10460.html">VUF10460</a>產(chǎn)品描述:VUF10460 is a non-imidazole histamine <b>H4</b> receptor agonist; binds to rat H4 receptor with a <b>pK<sub>i</sub></b> of 7.46.

IC50 & Target: pKi: 7.46 (H4)<sup>[1]</sup>

<i><b>In Vitro:</b></i> UF10460 binds to rat H3 and H4 receptor with pK<sub>i</sub> values of 5.75, and 7.46, respectively. VUF10460 displays approximately a 50-fold selectivity for the rat H4 receptor over the H3 receptor<sup>[1]</sup>.

<i><b>In Vivo:</b></i> HCl-induced rat gastric lesions is significantly enhanced by the H4 receptor agonists VUF10460. This effect is not modified by H4 receptor antagonist JNJ7777120<sup>[1]</sup>.<br><br>
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已為全球多個知名企業(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/vuf10460.html">www.medchemexpress.cn/vuf10460.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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