Department of Medicinal Chemistry, Jagiellonian University Medical College, Medyczna 9, 30-688 Kraków, Poland.
Biomolecules. 2024 Jul 4;14(7):797. doi: 10.3390/biom14070797.
The main protease (Mpro) of SARS-CoV-2 is an essential enzyme that plays a critical part in the virus's life cycle, making it a significant target for developing antiviral drugs. The inhibition of SARS-CoV-2 Mpro has emerged as a promising approach for developing therapeutic agents to treat COVID-19. This review explores the structure of the Mpro protein and analyzes the progress made in understanding protein-ligand interactions of Mpro inhibitors. It focuses on binding kinetics, origin, and the chemical structure of these inhibitors. The review provides an in-depth analysis of recent clinical trials involving covalent and non-covalent inhibitors and emerging dual inhibitors targeting SARS-CoV-2 Mpro. By integrating findings from the literature and ongoing clinical trials, this review captures the current state of research into Mpro inhibitors, offering a comprehensive understanding of challenges and directions in their future development as anti-coronavirus agents. This information provides new insights and inspiration for medicinal chemists, paving the way for developing more effective Mpro inhibitors as novel COVID-19 therapies.
新型冠状病毒主蛋白酶(Mpro)是一种至关重要的酶,在病毒生命周期中起着关键作用,因此成为开发抗病毒药物的重要靶点。抑制新型冠状病毒 Mpro 已成为开发治疗 COVID-19 的治疗药物的有前途的方法。本综述探讨了 Mpro 蛋白的结构,并分析了在理解 Mpro 抑制剂的蛋白-配体相互作用方面取得的进展。它重点介绍了结合动力学、起源和这些抑制剂的化学结构。该综述深入分析了涉及共价和非共价抑制剂以及针对新型冠状病毒 Mpro 的新兴双重抑制剂的最新临床试验。通过整合文献和正在进行的临床试验的结果,本综述捕捉到了目前对 Mpro 抑制剂的研究状况,全面了解了它们作为抗冠状病毒药物未来发展的挑战和方向。这些信息为药物化学家提供了新的见解和灵感,为开发更有效的 Mpro 抑制剂作为新型 COVID-19 疗法铺平了道路。