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COVID-19:潜在的再利用药物。

COVID-19: Potential Repurposing Drugs.

机构信息

Department of Clinical Tropical Medicine, Faculty of Tropical Medicine, Mahidol University, 420/6 Rajavithi Road, Rachatawee, Bangkok 10400, Thailand.

出版信息

Infect Disord Drug Targets. 2022;22(1):e110122191924. doi: 10.2174/1871526521666210301143441.

DOI:10.2174/1871526521666210301143441
PMID:33645490
Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is one of the most infectious diseases which has been caused by coronavirus in 2019 (COVID-19). It has widely spread worldwide and infected more than 28 million people in 215 countries, and more than 920,000 have now died from COVID-19. To date, no effective antiviral drugs or specific vaccines have been discovered yet. Considering this situation, the potential therapeutic antiviral drug targets for the COVID-19 are being repurposed to speed up the discovery of effective treatment. The most potential drug targets that are continuously being recommended include Favipiravir, Chloroquine, Hydroxychloroquine, and Remdesivir. Moreover, the antiviral target proteins and anti-host target proteins are being reported continuously. This review has summarized the current research studies on potential therapeutic drug targets that are being tested against the SARS-CoV-2. It will provide information related to potential repurposing drugs for overcoming COVID-19.

摘要

严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)是由冠状病毒引起的 2019 年(COVID-19)最具传染性的疾病之一。它已在全球范围内广泛传播,在 215 个国家感染了超过 2800 万人,目前已有超过 92 万人死于 COVID-19。迄今为止,尚未发现有效的抗病毒药物或特定疫苗。鉴于这种情况,正在重新利用有治疗潜力的抗病毒药物靶点,以加快有效治疗方法的发现。目前持续推荐的最有潜力的药物靶点包括法匹拉韦、氯喹、羟氯喹和瑞德西韦。此外,抗病毒目标蛋白和抗宿主目标蛋白也在不断被报道。这篇综述总结了目前针对 SARS-CoV-2 正在测试的潜在治疗药物靶点的研究。它将提供有关克服 COVID-19 的潜在再利用药物的信息。

相似文献

1
COVID-19: Potential Repurposing Drugs.COVID-19:潜在的再利用药物。
Infect Disord Drug Targets. 2022;22(1):e110122191924. doi: 10.2174/1871526521666210301143441.
2
Impact of repurposed drugs on the symptomatic COVID-19 patients.重新利用药物对有症状的 COVID-19 患者的影响。
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The Anatomy of the SARS-CoV-2 Biomedical Literature: Introducing the CovidX Network Algorithm for Drug Repurposing Recommendation.严重急性呼吸综合征冠状病毒2生物医学文献剖析:介绍用于药物重新利用推荐的CovidX网络算法
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Drug Discovery by Drug Repurposing: Combating COVID-19 in the 21st Century.药物重定位的药物发现:在 21 世纪抗击 COVID-19。
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Docking study of chloroquine and hydroxychloroquine interaction with RNA binding domain of nucleocapsid phospho-protein - an insight into the comparative efficacy of repurposing antiviral drugs.氯喹和羟氯喹与核衣壳磷酸蛋白 RNA 结合域相互作用的对接研究——重新利用抗病毒药物的相对疗效的深入了解。
J Biomol Struct Dyn. 2021 Aug;39(12):4243-4255. doi: 10.1080/07391102.2020.1775703. Epub 2020 Jul 6.
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Facts and Myths: Efficacies of Repurposing Chloroquine and Hydroxychloroquine for the Treatment of COVID-19.事实与误区:重新利用氯喹和羟氯喹治疗 COVID-19 的疗效。
Curr Drug Targets. 2020;21(16):1703-1721. doi: 10.2174/1389450121666200617133142.
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Small-molecule Antiviral Agents in Ongoing Clinical Trials for COVID-19.正在进行的COVID-19临床试验中的小分子抗病毒药物
Curr Drug Targets. 2021;22(17):1986-2005. doi: 10.2174/1389450122666210215112150.
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Effective drugs used to combat SARS-CoV-2 infection and the current status of vaccines.用于对抗 SARS-CoV-2 感染的有效药物和当前疫苗的状况。
Biomed Pharmacother. 2021 May;137:111330. doi: 10.1016/j.biopha.2021.111330. Epub 2021 Jan 28.
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Favipiravir at high doses has potent antiviral activity in SARS-CoV-2-infected hamsters, whereas hydroxychloroquine lacks activity.高剂量的法匹拉韦对感染 SARS-CoV-2 的仓鼠具有强大的抗病毒活性,而羟氯喹则没有活性。
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What makes (hydroxy)chloroquine ineffective against COVID-19: insights from cell biology.(羟)氯喹对抗 COVID-19 无效的原因:细胞生物学的见解。
J Mol Cell Biol. 2021 Jul 6;13(3):175-184. doi: 10.1093/jmcb/mjab016.

引用本文的文献

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May Interfere with the Interaction Between ACE2 and SARS-CoV-2 Spike Protein in vitro and Reduces Lung Inflammation in a Hamster Model of COVID-19.在体外可能干扰血管紧张素转换酶2(ACE2)与严重急性呼吸综合征冠状病毒2(SARS-CoV-2)刺突蛋白之间的相互作用,并减轻新冠病毒肺炎仓鼠模型中的肺部炎症。
J Inflamm Res. 2023 Oct 26;16:4867-4884. doi: 10.2147/JIR.S431222. eCollection 2023.
2
Repurposing clinically available drugs and therapies for pathogenic targets to combat SARS-CoV-2.重新利用临床可用药物和疗法针对致病靶点来对抗新型冠状病毒。
MedComm (2020). 2023 May 14;4(3):e254. doi: 10.1002/mco2.254. eCollection 2023 Jun.