首页> 外文期刊>Journal of the American Chemical Society >Synthesis of a 10,000-membered library of molecules resembling carpanone and discovery of vesicular traffic inhibitors
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Synthesis of a 10,000-membered library of molecules resembling carpanone and discovery of vesicular traffic inhibitors

机译:具有10,000个分子的类似于甲酮的分子文库的合成和水泡交通抑制剂的发现

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Split-and-pool synthesis of a 10,000-membered library of molecules resembling the natural product carpanone has been achieved. The synthesis features development of solid-phase multicomponent reactions between nitrogen nucleophiles, enones, and hydroxylamines, and a solid-phase application of the Huisgen cycloaddition affording substituted triazoles. The synthesis was performed in high-capacity (500 pm) polystyrene beads using a one bead-one stock solution strategy that enabled phenotypic screens of the resulting library. Using whole-cell fluorescence imaging, we discovered a series of molecules from the carpanone-based library that inhibit exocytosis from the Golgi apparatus. The most potent member of this series has an IC50 of 14 mu M. We also report structure-activity relationships for the molecules exhibiting this interesting phenotype. These inhibitors of exocytosis may be useful reagents for the study of vesicular traffic.
机译:已经实现了由10,000元组成的分子库的拆分和合并合成,该分子库类似于天然产物甲酮。该合成的特征在于氮亲核体,烯酮和羟胺之间的固相多组分反应的发展,以及Huisgen环加成的固相应用提供了取代的三唑。合成是在高容量(500 pm)聚苯乙烯珠粒中进行的,使用的是一种珠粒一储备液策略,该策略可对所得文库进行表型筛选。使用全细胞荧光成像,我们从基于甲酮的文库中发现了一系列抑制高尔基体细胞胞吐作用的分子。该系列中最有效的成员的IC50为14μM。我们还报告了表现出这种有趣表型的分子的构效关系。这些胞吐抑制剂可能是研究囊泡运输的有用试剂。

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