Al Adem Kenana, Shanti Aya, Stefanini Cesare, Lee Sungmun
Healthcare Engineering Innovation Center, Department of Biomedical Engineering, Khalifa University of Science and Technology, Abu Dhabi 127788, UAE.
Khalifa University's Center for Biotechnology, Khalifa University of Science and Technology, Abu Dhabi 127788, UAE.
Pharmaceuticals (Basel). 2020 Dec 8;13(12):447. doi: 10.3390/ph13120447.
Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), a virus belonging to the Coronavirus family, is now known to cause Coronavirus Disease (Covid-19) which was first recognized in December 2019. Covid-19 leads to respiratory illnesses ranging from mild infections to pneumonia and lung failure. Strikingly, within a few months of its first report, Covid-19 has spread worldwide at an exceptionally high speed and it has caused enormous human casualties. As yet, there is no specific treatment for Covid-19. Designing inhibitory drugs that can interfere with the viral entry process constitutes one of the main preventative therapies that could combat SARS-CoV-2 infection at an early stage. In this review, we provide a brief introduction of the main features of coronaviruses, discuss the entering mechanism of SARS-CoV-2 into human host cells and review small molecules that inhibit SARS-CoV-2 entry into host cells. Specifically, we focus on small molecules, identified by experimental validation and/or computational prediction, that target the SARS-CoV-2 spike protein, human angiotensin converting enzyme 2 (ACE2) receptor and the different host cell proteases that activate viral fusion. Given the persistent rise in Covid-19 cases to date, efforts should be directed towards validating the therapeutic effectiveness of these identified small molecule inhibitors.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)是一种属于冠状病毒科的病毒,目前已知它会引发冠状病毒病(Covid-19),该病于2019年12月首次被发现。Covid-19会导致从轻度感染到肺炎和肺衰竭等一系列呼吸道疾病。引人注目的是,在首次报告后的几个月内,Covid-19已以极高的速度在全球传播,并造成了巨大的人员伤亡。截至目前,尚无针对Covid-19的特效治疗方法。设计能够干扰病毒进入过程的抑制性药物是可以在早期对抗SARS-CoV-2感染的主要预防疗法之一。在本综述中,我们简要介绍了冠状病毒的主要特征,讨论了SARS-CoV-2进入人类宿主细胞的机制,并综述了抑制SARS-CoV-2进入宿主细胞的小分子。具体而言,我们重点关注通过实验验证和/或计算预测确定的、靶向SARS-CoV-2刺突蛋白、人类血管紧张素转换酶2(ACE2)受体以及激活病毒融合的不同宿主细胞蛋白酶的小分子。鉴于迄今为止Covid-19病例持续增加,应致力于验证这些已确定的小分子抑制剂的治疗效果。