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An efficient and convenient microwave-assisted chemical synthesis of (thio)xanthones with additional in vitro and in silico characterization

机译:高效,便捷的微波辅助化学合成(硫代)氧杂蒽酮,并具有体外和计算机表征

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摘要

Xanthones and their thio-derivatives are a class of pleiotropic compounds with various reported pharmacological and biological activities. Although these activities are mainly determined in laboratory conditions, the class itself has a great potential to be utilized as promising chemical scaffold for the synthesis of new drug candidates. One of the main obstacles in utilization of these compounds was related to the difficulties in their chemical synthesis. Most of the known methods require two steps, and are limited to specific reagents not applicable to a large number of starting materials. In this paper a new and improved method for chemical synthesis of xanthones is presented. By applying a new procedure, we have successfully obtained these compounds with the desired regioselectivity in a shorter reaction time (50 s) and with better yield (>80%). Finally, the preliminary in vitro screenings on different bacterial species and cytotoxicity assessment, as well as in silico activity evaluation were performed. The obtained results confirm potential pharmacological use of this class of molecules.
机译:氧杂蒽酮及其硫代衍生物是一类具有多种药理和生物学活性的多效化合物。尽管这些活动主要是在实验室条件下确定的,但该类本身具有很大的潜力,可以用作合成新药物候选物的有前途的化学支架。利用这些化合物的主要障碍之一与它们化学合成的困难有关。大多数已知方法需要两个步骤,并且限于不适用于大量起始材料的特定试剂。本文提出了一种新的和改进的化学合成improved吨的方法。通过应用新程序,我们已经在较短的反应时间(50 s)和较高的收率(> 80%)中成功获得了具有所需区域选择性的化合物。最后,进行了不同细菌种类的初步体外筛选和细胞毒性评估以及计算机活性评估。获得的结果证实了这类分子的潜在药理学用途。

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