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首页> 外文期刊>Bulletin of the Korean Chemical Society >Microwave-Accelerated Click Chemistry: Expeditious Synthesis of Novel Triazole-linked Salicylic β-D-O-Glycosides with PTPIB Inhibitory Activity
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Microwave-Accelerated Click Chemistry: Expeditious Synthesis of Novel Triazole-linked Salicylic β-D-O-Glycosides with PTPIB Inhibitory Activity

机译:微波加速点击化学:快速合成具有PTPIB抑制活性的新型三唑连接的水杨酸β-D-O-糖苷

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摘要

The incorporation of microwave irradiation with the prevalent "click chemistry" is currently of considerable synthetic interest. We describe here the introduction of such laboratorial shortcut into carbohydrate-based drug discovery, resulting in the rapid formation of a series of triazole-linked salicylic β-D-O-glycosides with biological activities. All "clicked" products were achieved in excellent yields (≈ 90%) within only a quarter. In addition, based on the structural characteristics of the afforded glycomimetics, their inhibitory activities were evaluated toward protein tyrosine phosphatases 1B (PTP1B) and a panel of homologous protein tyrosine phosphatases (PTPs). Docking simulation was also conducted to plausibly propose binding modes of this glycosyl salicylate series with the enzymatic target.
机译:微波辐射与流行的“点击化学”的结合目前具有相当大的合成意义。我们在这里描述了将这种实验室快捷方式引入基于碳水化合物的药物发现中,从而导致一系列具有生物活性的三唑连接的水杨酸β-D-O-糖苷快速形成。在短短四分之一的时间内,所有“点击”产品均以优异的产量(约90%)获得了成功。另外,基于所提供的糖模拟物的结构特征,评估了它们对蛋白质酪氨酸磷酸酶1B(PTP1B)和一组同源蛋白质酪氨酸磷酸酶(PTP)的抑制活性。还进行了对接模拟以合理地提出该糖基水杨酸酯系列与酶促靶标的结合模式。

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