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鉴定天然化合物作为潜在的新型冠状病毒主要蛋白酶(Mpro)抑制剂:一项全面研究及证据

Identification of Natural Compounds as Potential COVID-19 Main Protease (Mpro) Inhibitors: A Comprehensive Study and Evidence.

作者信息

Devi Arti, Dwibedi Vagish, Jain Sahil, Kaur Gursharan, Khan Zaved Ahmed, Mandal Sudip Kumar, Shiven Aditya, Shah Kamal, Dewangan Hitesh Kumar, Rath Santosh Kumar

机构信息

University Institute of Biotechnology, Chandigarh University, Mohali, Punjab, India.

Faculty of Life Sciences Baba Farid College, Muktsar Road, Bathinda, Punjab, India.

出版信息

Curr Pharm Des. 2025;31(30):2416-2437. doi: 10.2174/0113816128344055250220100720.

DOI:10.2174/0113816128344055250220100720
PMID:40108907
Abstract

SARS-CoV-2, the virus responsible for COVID-19, has resulted in a devastating global impact with millions of lives lost. Remdesivir and 2-DG are among the few drugs authorized for emergency use against COVID-19, but concerns about their efficacy and side effects persist. Vaccines have been developed and approved, yet the emergence of viral mutations has raised questions about their effectiveness against new variants. Natural compounds with antiviral properties have shown promise in combating SARS-CoV-2. The review highlights the potential of medicinal plant compounds, particularly in targeting the virus' main protease, a crucial component for viral replication. Natural, plant-derived compounds represent a promising avenue for COVID-19 therapeutics. Further clinical validation is necessary to ascertain their efficacy and safety in treating COVID-19. This underscores the importance of continued research into alternative treatments for combating this global health crisis. This review examines the potential of natural, plant-derived compounds as safe and cost-effective alternatives for combating COVID-19. It summarizes the pathogenesis of SARS-CoV- 2 and the ongoing drug studies and identifies natural compounds with known antiviral properties. Additionally, it explores the potential of medicinal plant compounds in targeting the SARS-CoV-2 main protease through and molecular docking studies.

摘要

导致新冠肺炎的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)已在全球造成毁灭性影响,数百万人丧生。瑞德西韦和2-脱氧-D-葡萄糖是少数被批准用于紧急治疗新冠肺炎的药物,但人们对其疗效和副作用的担忧依然存在。疫苗已研发并获批,但病毒突变的出现引发了对其针对新变种有效性的质疑。具有抗病毒特性的天然化合物在对抗SARS-CoV-2方面显示出前景。该综述强调了药用植物化合物的潜力,特别是在靶向病毒主要蛋白酶方面,这是病毒复制的关键组成部分。天然的、植物来源的化合物是治疗新冠肺炎的一个有前景的途径。需要进一步的临床验证来确定它们在治疗新冠肺炎方面的疗效和安全性。这凸显了继续研究对抗这一全球健康危机的替代疗法的重要性。本综述探讨了天然的、植物来源的化合物作为对抗新冠肺炎的安全且经济有效的替代方案的潜力。它总结了SARS-CoV-2的发病机制以及正在进行的药物研究,并确定了具有已知抗病毒特性的天然化合物。此外,它还通过 和分子对接研究探索了药用植物化合物靶向SARS-CoV-2主要蛋白酶的潜力。

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Ther Deliv. 2024;15(9):685-698. doi: 10.1080/20415990.2024.2380239. Epub 2024 Aug 12.
2
Inhibition of hepatocellular carcinoma cell proliferation through regulation of the Cell Cycle, AGE-RAGE, and Leptin signaling pathways by a compound formulation comprised of andrographolide, wogonin, and oroxylin A derived from Andrographis Paniculata(Burm.f.) Nees.穿心莲(爵床科穿心莲属)中提取的穿心莲内酯、汉黄芩素和木犀草素的化合物配方通过调节细胞周期、晚期糖基化终产物受体(AGE-RAGE)和瘦素信号通路抑制肝癌细胞增殖。
J Ethnopharmacol. 2024 Jul 15;329:118001. doi: 10.1016/j.jep.2024.118001. Epub 2024 Mar 11.
3
Delivery of nano-emulgel carrier: optimization, evaluation and anti-inflammation estimations for osteoarthritis.纳米乳凝胶载体的递送:骨关节炎的优化、评估及抗炎评估
Ther Deliv. 2024 Mar;15(3):181-192. doi: 10.4155/tde-2023-0109. Epub 2024 Feb 15.
4
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Chem Biodivers. 2024 Mar;21(3):e202301468. doi: 10.1002/cbdv.202301468. Epub 2024 Feb 22.
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Review on the Artificial Intelligence-based Nanorobotics Targeted Drug Delivery System for Brain-specific Targeting.基于人工智能的脑特异性靶向纳米机器人给药系统综述
Curr Pharm Des. 2023;29(44):3519-3531. doi: 10.2174/0113816128279248231210172053.
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Cancer Immunol Immunother. 2023 Oct;72(10):3279-3292. doi: 10.1007/s00262-023-03487-3. Epub 2023 Jul 18.