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Sustainable, three-component, one-pot procedure to obtain active anti-flavivirus agents

机译:可持续,三组分,单罐程序,以获得活性抗黄病毒剂

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The mosquito-borne viruses belonging to the genus Flavivirus such as Dengue virus (DENV) and Zika virus (ZIKV) cause human infections ranging from mild flu-like symptoms to hemorrhagic fevers, hepatitis, and neuropathies. To date, there are vaccines only for few flaviviruses while no effective treatments are available. Pyridobenzothiazole (PBTZ) derivatives are a class of compounds endowed with a promising broad-spectrum anti-flavivirus activity and most of them have been reported as potent inhibitors of the flaviviral NS5 polymerase. However, synthesis of PBTZ analogues entails a high number of purification steps, the use of hazardous reagents and environmentally unsustainable generation of waste. Considering the promising antiviral activity of PBTZ analogues which require further exploration, in this work, we report the development of a new and sustainable three-component reaction (3CR) that can be combined with a basic hydrolysis in a one-pot procedure to obtain the PBTZ scaffold, thus reducing the number of synthetic steps, improving yields and saving time. 3CR was significantly explored in order to demonstrate its wide scope by using different starting materials. In addition, taking advantage of these procedures, we next designed and synthesized a new set of PBTZ analogues that were tested as anti-DENV-2 and anti-ZIKV agents. Compound 22 inhibited DENV-2 NS5 polymerase with an IC50 of 10.4 mu M and represented the best anti-flavivirus compound of the new series by inhibiting DENV-2- and ZIKV-infected cells with EC50 values of 1.2 and 5.0 mu M, respectively, that translates into attractive selectivity indexes (SI - 83 and 20, respectively). These results strongly reaffirm PBTZ derivatives as promising anti-flavivirus agents that now can be synthesized through a convenient and sustainable 3CR in order to obtain more potent compounds for further pre-clinical development studies. (C) 2020 Elsevier Masson SAS. All rights reserved.
机译:蚊子传播的病毒属于黄病毒属,如登革热病毒(DENV)和寨卡病毒(ZIKV),可引起人类感染,从轻微的流感样症状到出血热、肝炎和神经病变。迄今为止,只有少数黄病毒的疫苗,但没有有效的治疗方法。吡啶苯并噻唑(PBTZ)衍生物是一类具有广谱抗黄病毒活性的化合物,其中大多数被报道为黄病毒NS5聚合酶的有效抑制剂。然而,PBTZ类似物的合成需要大量的纯化步骤、使用危险试剂和环境不可持续的废物产生。考虑到PBTZ类似物有很好的抗病毒活性,需要进一步探索,在这项工作中,我们报告了一种新的可持续的三组分反应(3CR)的开发,该反应可以与一锅法中的碱性水解相结合,以获得PBTZ支架,从而减少合成步骤的数量,提高产率并节省时间。为了通过使用不同的起始材料来展示其广泛的应用范围,3CR得到了显著的探索。此外,利用这些程序,我们接下来设计并合成了一组新的PBTZ类似物,作为抗DENV-2和抗ZIKV药物进行了测试。化合物22以10.4μM的IC50抑制DENV-2 NS5聚合酶,并通过分别以1.2和5.0μM的EC50值抑制DENV-2和ZIKV感染的细胞,代表了新系列中最好的抗黄病毒化合物,这转化为有吸引力的选择性指数(分别为SI-83和20)。这些结果有力地证实了PBTZ衍生物是一种有前途的抗黄病毒药物,现在可以通过一种方便且可持续的3CR合成,以获得更有效的化合物,用于进一步的临床前开发研究。(C) 2020年爱思唯尔马森SAS。版权所有。

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