冠状病毒
穗蛋白
2019年冠状病毒病(COVID-19)
Spike(软件开发)
药理学
病毒学
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
计算生物学
医学
生物
计算机科学
疾病
传染病(医学专业)
内科学
软件工程
作者
Xing Huang,Heng Gao,Jiwei Zhang,Peng Zhan,Xinyong Liu
标识
DOI:10.1080/13543776.2025.2494860
摘要
In the 5 years since the outbreak of SARS-CoV-2, numerous methods and design strategies have been employed to develop innovative therapeutics against coronaviruses. Among these approaches, inhibitors targeting both the ACE2 receptor and the S protein have gained significant interest due to their potential in blocking various coronaviruses. Despite facing challenges similar to other protein-protein interaction inhibitors, progress has been made in developing these inhibitors through virtual screening, covalent protein binding, and peptide modification strategies. However, obstacles persist in clinical translation, necessitating a multidisciplinary strategy that integrates state-of-the-art methodologies to optimize S-ACE2 interface-targeted drug discovery.
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