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Real-TimeBiological Annotation of Synthetic Compounds

机译:即时的合成化合物的生物注释

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摘要

Organic chemists are able to synthesize molecules in greater number and chemical complexity than ever before. Yet, a majority of these compounds go untested in biological systems, and those that do are often tested long after the chemist can incorporate the results into synthetic planning. We propose the use of high-dimensional “multiplex” assays, which are capable of measuring thousands of cellular features in one experiment, to annotate rapidly and inexpensively the biological activities of newly synthesized compounds. This readily accessible and inexpensive “real-time” profiling method can be used in a prospective manner to facilitate, for example, the efficient construction of performance-diverse small-molecule libraries that are enriched in bioactives. Here, we demonstrate this concept by synthesizing ten triads of constitutionally isomeric compounds via complexity-generating photochemical and thermal rearrangements and measuring compound-induced changes in cellular morphology via an imaging-based “cell painting” assay. Our results indicate that real-time biological annotation caninform optimization efforts and library syntheses by illuminatingtrends relating to biological activity that would be difficult topredict if only chemical structure were considered. We anticipatethat probe and drug discovery will benefit from the use of optimizationefforts and libraries that implement this approach.
机译:有机化学家能够以前所未有的数量和化学复杂性合成分子。但是,这些化合物中的大多数在生物系统中未经测试,经常在化学家将结果纳入合成计划后很长时间才进行测试。我们建议使用能够在一个实验中测量数千个细胞特征的高维“多重”测定法,以快速,廉价地注释新合成化合物的生物学活性。这种易于访问且便宜的“实时”配置方法可以以预期的方式使用,以促进例如高效构建富含生物活性物质的性能多样化的小分子文库。在这里,我们通过产生光化学和热重排的复杂性合成十个三联体的组成异构化合物,并通过基于成像的“细胞绘画”测定法测量化合物诱导的细胞形态变化,从而证明了这一概念。我们的结果表明,实时生物注释可以通过照亮来告知优化工作和库综合与生物活性有关的趋势,很难预测是否仅考虑化学结构。我们期待探针和药物发现将从优化中受益努力和实现此方法的库。

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