State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, No. 38, Xueyuan Road, Haidian District, Beijing 100191, China.
J Med Chem. 2020 Dec 24;63(24):15371-15388. doi: 10.1021/acs.jmedchem.0c01348. Epub 2020 Nov 17.
Fatal infectious diseases caused by HIV-1, influenza A virus, Ebola virus, and currently pandemic coronavirus highlight the great need for the discovery of antiviral agents in mechanisms different from current viral replication-targeted approaches. Given the critical role of virus-host interactions in the viral life cycle, the development of entry or shedding inhibitors may expand the current repertoire of antiviral agents; the combination of antireplication inhibitors and entry or shedding inhibitors would create a multifaceted drug cocktail with a tandem antiviral mechanism. Therefore, we provide critical information about triterpenoids as potential antiviral agents targeting entry and release, focusing specifically on the emerging aspect of triterpenoid-mediated inhibition of a variety of virus-host membrane fusion mechanisms via a trimer-of-hairpin motif. These properties of triterpenoids supply their host an evolutionary advantage for chemical defense and may protect against an increasingly diverse array of viruses infecting mammals, providing a direction for antiviral drug discovery.
由 HIV-1、甲型流感病毒、埃博拉病毒和目前流行的冠状病毒引起的致命传染病突出表明,非常需要发现与目前针对病毒复制的方法不同的抗病毒药物。鉴于病毒-宿主相互作用在病毒生命周期中的关键作用,开发进入或脱落抑制剂可能会扩大目前抗病毒药物的种类;将复制抑制剂和进入或脱落抑制剂联合使用,将创建一种具有双重抗病毒机制的多方面药物鸡尾酒。因此,我们提供了有关三萜类化合物作为针对进入和释放的潜在抗病毒药物的关键信息,特别关注三萜类化合物通过三聚体发夹基序介导抑制多种病毒-宿主膜融合机制的新出现方面。三萜类化合物的这些特性为宿主提供了化学防御的进化优势,可能有助于预防感染哺乳动物的病毒种类不断增加,为抗病毒药物的发现提供了一个方向。