严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
2019年冠状病毒病(COVID-19)
大流行
病毒进入
病毒学
2019-20冠状病毒爆发
寄主(生物学)
酶
病毒
生物
细胞生物学
化学
医学
生物化学
遗传学
病毒复制
内科学
传染病(医学专业)
疾病
爆发
作者
Young‐Hee Shin,Kiyoung Jeong,Jihye Lee,Hyo‐Jung Lee,Junhyeong Yim,Jonghoon Kim,Seungtaek Kim,Seung Bum Park
标识
DOI:10.1002/anie.202115695
摘要
The emergence of SARS-CoV-2 variants is a significant concern in developing effective therapeutics and vaccines in the middle of the ongoing COVID-19 pandemic. Here, we have identified a novel small molecule that inhibited the interactions between SARS-CoV-2 spike RBDs and ACE2 by modulating ACE2 without impairing its enzymatic activity necessary for normal physiological functions. Furthermore, the identified compounds suppressed viral infection in cultured cells by inhibiting the entry of ancestral and variant SARS-CoV-2. Our study suggests that targeting ACE2 could be a novel therapeutic strategy to inhibit SARS-CoV-2 entry into host cells and prevent the development of COVID-19.
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