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首页> 外文期刊>The Journal of Organic Chemistry >Detection of Lysosome by a Fluorescent Heterocycle: Development of Fused Pyrido-Imidazo-Indole Framework via Cu-Catalyzed Tandem N-Arylation
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Detection of Lysosome by a Fluorescent Heterocycle: Development of Fused Pyrido-Imidazo-Indole Framework via Cu-Catalyzed Tandem N-Arylation

机译:荧光杂环检测溶酶体:通过Cu催化串联N-芳基熔融吡啶 - 咪唑 - 吲哚框架的发育

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摘要

Fluorescent active small molecules for organelle-specific bioimaging are in great demand. We synthesized 20 different pyrido-imidazo-indole fused heterocycles (6-5-5-6 ring) via copper catalyzed tandem N-arylation reaction in moderate to good yields. Due to decent fluorescent property, lysosome-directing moieties were attached on two of these heterocycles. Delightfully, those molecules tracked lysosome with bright blue fluorescence and colocalized with a known lysosome marker (Lysotracker Red) in human/murine cells. Therefore, it may be considered as a rapid (10 min) lysosome staining probe.
机译:用于细胞器特异性生物成像的荧光活性小分子具有很大的需求。 通过中等至良好的产率,通过铜催化的串联N-芳基化反应合成20种不同的吡啶-Imidazo-Indole融合杂环(6-5-5-6环)。 由于体面的荧光特性,将溶酶体引导部分连接在其中两种杂环上。 令人愉快地,这些分子跟踪溶酶体,用鲜艳的蓝色荧光,并在人/鼠细胞中用已知的溶酶体标记物(Lysotracker Red)结合。 因此,它可以被认为是快速(10分钟)溶酶体染色探针。

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