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首页> 外文期刊>European Journal of Pharmacology: An International Journal >Flavonols as potential antiviral drugs targeting SARS-CoV-2 proteases (3CL(pro) and PLpro), spike protein, RNA-dependent RNA polymerase (RdRp) and angiotensin-converting enzyme II receptor (ACE2)
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Flavonols as potential antiviral drugs targeting SARS-CoV-2 proteases (3CL(pro) and PLpro), spike protein, RNA-dependent RNA polymerase (RdRp) and angiotensin-converting enzyme II receptor (ACE2)

机译:黄酮醇作为靶向SARS-COV-2蛋白酶(3CL(PRO)和PLPRO),穗蛋白,RNA依赖性RNA聚合酶(RDRP)和血管紧张素转换酶II受体(ACE2)的潜在抗病毒药物(ACE2)

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摘要

The novel coronavirus outbreak (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) represents the actual greatest global public health crisis. The lack of efficacious drugs and vaccines against this viral infection created a challenge for scientific researchers in order to find effective solutions. One of the promising therapeutic approaches is the search for bioactive molecules with few side effects that display antiviral properties in natural sources like medicinal plants and vegetables. Several computational and experimental studies indicated that flavonoids especially flavonols and their derivatives constitute effective viral enzyme inhibitors and possess interesting antiviral activities. In this context, the present study reviews the efficacy of many dietary flavonols as potential antiviral drugs targeting the SARS-CoV-2 enzymes and proteins including Chymotrypsin-Like Protease (3CL(pro)), Papain Like protease (PLpro), Spike protein (S protein) and RNA-dependent RNA polymerase (RdRp), and also their ability to interact with the angiotensin-converting enzyme II (ACE2) receptor. The relationship between flavonol structures and their SARS-CoV-2 antiviral effects were discussed. On the other hand, the immunomodulatory, the anti-inflammatory and the antiviral effects of secondary metabolites from this class of flavonoids were reported. Also, their bioavailability limitations and toxicity were predicted.
机译:新型冠状病毒2019冠状病毒疾病(COVID-19)由严重急性呼吸综合征冠状病毒2(SARS COV-2)引起,是全球最大的公共卫生危机。缺乏有效的药物和疫苗来对抗这种病毒感染,这给科研人员寻找有效的解决方案带来了挑战。其中一个有希望的治疗方法是寻找副作用小的生物活性分子,在药用植物和蔬菜等天然来源中显示抗病毒特性。一些计算和实验研究表明,黄酮类化合物尤其是黄酮醇及其衍生物是有效的病毒酶抑制剂,具有有趣的抗病毒活性。在此背景下,本研究综述了许多膳食黄酮醇作为潜在抗病毒药物针对SARS-CoV-2酶和蛋白质的功效,包括糜蛋白酶样蛋白酶(3CL(pro))、木瓜蛋白酶样蛋白酶(PLpro)、棘突蛋白(S蛋白)和RNA依赖性RNA聚合酶(RdRp),以及它们与血管紧张素转换酶II(ACE2)受体相互作用的能力。讨论了黄酮醇结构与SARS-CoV-2抗病毒作用的关系。另一方面,这类黄酮类化合物的次级代谢产物具有免疫调节、抗炎和抗病毒作用。此外,还预测了它们的生物利用度限制和毒性。

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