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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >SYNTHESIS OF CHEMICAL-BIOLOGY TOOLS ENABLING IN VIVO IMAGING AND ANALYSIS OF EPIGALLOCATECHIN GALLATE
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SYNTHESIS OF CHEMICAL-BIOLOGY TOOLS ENABLING IN VIVO IMAGING AND ANALYSIS OF EPIGALLOCATECHIN GALLATE

机译:化学生物学工具的合成能够进行体内成像和ePigallocateChin pallate的分析

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摘要

(-)-Epigallocatechin gallate (EGCg) has multiple bioactivities, and imaging/analytical tools are required for drug development studies. Here we present full details of our synthetic studies aimed at providing building blocks for development of such tools, including a concise synthesis of model compound 5,7-dideoxyEGCg (DOEGCg, 2) and an asymmetric synthesis of 6-(5-aminopenty1)-5,7-deoxyepigallocatechin gallate (APDOEGCg, 4), which contains a reactive terminal amino group. To demonstrate its utility, APDOEGCg (4) was efficiently converted to a fluorescent probe 53 by linking it to a fluorescein derivative, Tokyo Green, via the amino group. We confirmed that 53 is suitable for in vivo imaging studies. We also prepared an immunogen 56 by conjugation of 4 to human serum albumin carrier protein via a glutaraldehyde linker, and we used 56 to raise anti-EGCg antiserum in mice. The fluorescent probe and antiserum should be useful tools for biochemical investigations of the localization and target sites of EGCg. APDOEGCg should also be available for developing other novel tools for biochemical studies of catechins.
机译:(-)-表没食子儿茶素没食子酸酯(EGCg)具有多种生物活性,药物开发研究需要成像/分析工具。在这里,我们详细介绍了我们的合成研究,旨在为此类工具的开发提供基础,包括模型化合物5,7-二脱氧EGCG(DOEGCg,2)的简明合成和6-(5-氨基戊烯基)-5,7-脱氧猪没食子酸没食子酸酯(APDOEGCg,4)的不对称合成,其中包含一个反应性末端氨基。为了证明其效用,通过氨基将APDOEGCg(4)连接到荧光素衍生物东京绿,有效地将其转化为荧光探针53。我们确认53适用于活体成像研究。我们还通过戊二醛连接物将4与人血清白蛋白载体蛋白结合制备了免疫原56,并使用56在小鼠中提高抗EGCg抗血清。荧光探针和抗血清应该是EGCg定位和靶点生化研究的有用工具。APDOEGCg还可用于开发儿茶素生化研究的其他新工具。

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