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抗新型冠状病毒潜在药物研发的最新进展。

Recent progress in the development of potential drugs against SARS-CoV-2.

作者信息

Chen Jianmin, Ali Fayaz, Khan Imran, Zhu Yi Zhun

机构信息

School of Pharmacy and State Key Laboratory of Quality Research in Chinese Medicine, Macau University of Science & Technology Avenida Wai Long, Taipa, 999078, Macau.

State Key Laboratory of Quality Research in Chinese Medicine, Macau University of Science & Technology Avenida Wai Long, Taipa, 999078, Macau.

出版信息

Curr Res Pharmacol Drug Discov. 2021;2:100057. doi: 10.1016/j.crphar.2021.100057. Epub 2021 Sep 14.

DOI:10.1016/j.crphar.2021.100057
PMID:34870155
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8437701/
Abstract

SARS-CoV-2, a newly emerged and highly pathogenic coronavirus, is identified as the causal agent of Coronavirus Disease (2019) (COVID-19) in the late December 2019, in China. The virus has rapidly spread nationwide and spilled over to the other countries around the globe, resulting in more than 120 million infections and 2.6 million deaths until the time of this review. Unfortunately, there are still no specific drugs available against this disease, and it is very necessary to call upon more scientists to work together to stop a further spread. Hence, the recent progress in the development of drugs may help scientific community quickly understand current research status and further develop new effective drugs. Herein, we summarize the cellular entry and replication process of this virus and discuss the recent development of potential viral based drugs that target bio-macromolecules in different stages of the viral life cycle, especially S protein, 3CL, PL, RdRp and helicase.

摘要

严重急性呼吸综合征冠状病毒2(SARS-CoV-2)是一种新出现的高致病性冠状病毒,于2019年12月底在中国被确定为冠状病毒病(2019)(COVID-19)的病原体。该病毒已在全国迅速传播,并蔓延至全球其他国家,截至本综述撰写时,已导致超过1.2亿人感染和260万人死亡。不幸的是,目前仍没有针对这种疾病的特效药物,非常有必要呼吁更多科学家共同努力阻止疫情进一步蔓延。因此,近期药物研发的进展可能有助于科学界快速了解当前的研究状况,并进一步开发新的有效药物。在此,我们总结了该病毒的细胞进入和复制过程,并讨论了近期针对病毒生命周期不同阶段生物大分子的潜在病毒靶向药物的研发进展,特别是针对刺突蛋白(S蛋白)、3C样蛋白酶(3CL)、木瓜蛋白酶样蛋白酶(PL)、RNA依赖性RNA聚合酶(RdRp)和解旋酶的药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c42/8663967/d96c5b3e8069/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c42/8663967/d96c5b3e8069/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c42/8663967/d96c5b3e8069/gr1.jpg

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本文引用的文献

1
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RSC Adv. 2020 Apr 21;10(27):15775-15783. doi: 10.1039/d0ra01899f.
2
extract and baicalein inhibit replication of SARS-CoV-2 and its 3C-like protease .黄芩提取物和黄芩素抑制 SARS-CoV-2 及其 3CL 样蛋白酶的复制。
J Enzyme Inhib Med Chem. 2021 Dec;36(1):497-503. doi: 10.1080/14756366.2021.1873977.
3
Enfuvirtide, an HIV-1 fusion inhibitor peptide, can act as a potent SARS-CoV-2 fusion inhibitor: an drug repurposing study.恩夫韦肽,一种 HIV-1 融合抑制剂肽,可作为一种有效的 SARS-CoV-2 融合抑制剂:药物再利用研究。
Eur J Med Chem. 2022 Dec 15;244:114803. doi: 10.1016/j.ejmech.2022.114803. Epub 2022 Oct 3.
4
COVID-19 therapy, from lung disease to systemic disorder.新冠病毒疾病治疗:从肺部疾病到全身性疾病
Curr Res Pharmacol Drug Discov. 2022;3:100099. doi: 10.1016/j.crphar.2022.100099. Epub 2022 Apr 1.
5
[Nirmatrelvir plus ritonavir (Paxlovid) a potent SARS-CoV-2 3CLpro protease inhibitor combination].[奈玛特韦片/利托那韦片组合包装(帕罗韦德),一种有效的严重急性呼吸综合征冠状病毒2 3CL蛋白酶抑制剂组合]
Rev Esp Quimioter. 2022 Jun;35(3):236-240. doi: 10.37201/req/002.2022. Epub 2022 Feb 21.
J Biomol Struct Dyn. 2022 Aug;40(12):5566-5576. doi: 10.1080/07391102.2021.1871958. Epub 2021 Jan 13.
4
Humanized single domain antibodies neutralize SARS-CoV-2 by targeting the spike receptor binding domain.人源化单域抗体通过靶向刺突受体结合域中和 SARS-CoV-2。
Nat Commun. 2020 Sep 10;11(1):4528. doi: 10.1038/s41467-020-18387-8.
5
Molecular Docking and Virtual Screening Based Prediction of Drugs for COVID-19.基于分子对接和虚拟筛选的 COVID-19 药物预测。
Comb Chem High Throughput Screen. 2021;24(5):716-728. doi: 10.2174/1386207323666200814132149.
6
Repurposing of known anti-virals as potential inhibitors for SARS-CoV-2 main protease using molecular docking analysis.利用分子对接分析将已知抗病毒药物重新用作严重急性呼吸综合征冠状病毒2主蛋白酶的潜在抑制剂。
Bioinformation. 2020 Apr 30;16(4):301-306. doi: 10.6026/97320630016301. eCollection 2020.
7
HIV/SARS-CoV-2 coinfection: A global perspective.HIV/SARS-CoV-2 合并感染:全球视角。
J Med Virol. 2021 Feb;93(2):726-732. doi: 10.1002/jmv.26321. Epub 2020 Jul 28.
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N Engl J Med. 2021 Feb 25;384(8):693-704. doi: 10.1056/NEJMoa2021436. Epub 2020 Jul 17.
9
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Antiviral Res. 2020 Oct;182:104868. doi: 10.1016/j.antiviral.2020.104868. Epub 2020 Jul 10.
10
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Anal Chem. 2020 Jul 21;92(14):9895-9900. doi: 10.1021/acs.analchem.0c01394. Epub 2020 Jul 2.