• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Drugs against SARS-CoV-2: What do we know about their mode of action?抗 SARS-CoV-2 药物:它们的作用机制我们了解多少?
Rev Med Virol. 2020 Nov;30(6):1-10. doi: 10.1002/rmv.2143. Epub 2020 Aug 11.
2
Repurposed Antiviral Drugs for the Treatment of COVID-19: Syntheses, Mechanism of Infection and Clinical Trials.用于治疗新冠肺炎的抗病毒药物再利用:合成、感染机制与临床试验
Mini Rev Med Chem. 2021;21(9):1123-1143. doi: 10.2174/1389557521666201222145842.
3
Cysteamine with In Vitro Antiviral Activity and Immunomodulatory Effects Has the Potential to Be a Repurposing Drug Candidate for COVID-19 Therapy.具有体外抗病毒活性和免疫调节作用的半胱胺有可能成为治疗 COVID-19 的重新定位药物候选物。
Cells. 2021 Dec 24;11(1):52. doi: 10.3390/cells11010052.
4
Efficacy and safety of nitazoxanide plus atazanavir/ritonavir for the treatment of moderate to severe COVID-19 (NACOVID): A structured summary of a study protocol for a randomised controlled trial.尼他唑胺联合阿扎那韦/利托那韦治疗中重度 COVID-19(NACOVID)的疗效和安全性:一项随机对照试验研究方案的结构化总结。
Trials. 2021 Jan 4;22(1):3. doi: 10.1186/s13063-020-04987-8.
5
Network analysis and molecular mapping for SARS-CoV-2 to reveal drug targets and repurposing of clinically developed drugs.针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的网络分析和分子图谱绘制,以揭示药物靶点和临床开发药物的重新利用。
Virology. 2021 Mar;555:10-18. doi: 10.1016/j.virol.2020.12.006. Epub 2020 Dec 30.
6
Pharmacological inhibition of fatty acid synthesis blocks SARS-CoV-2 replication.药物抑制脂肪酸合成可阻断 SARS-CoV-2 复制。
Nat Metab. 2021 Nov;3(11):1466-1475. doi: 10.1038/s42255-021-00479-4. Epub 2021 Sep 27.
7
Repurposed pharmacological agents for the potential treatment of COVID-19: a literature review.重新利用药理学药物治疗 COVID-19 的潜力:文献综述。
Respir Res. 2021 Nov 27;22(1):304. doi: 10.1186/s12931-021-01885-8.
8
Understanding Individual SARS-CoV-2 Proteins for Targeted Drug Development against COVID-19.理解单个 SARS-CoV-2 蛋白以针对 COVID-19 开发靶向药物。
Mol Cell Biol. 2021 Aug 24;41(9):e0018521. doi: 10.1128/MCB.00185-21.
9
Recent Approaches of Repositioning and Traditional Drugs for the Treatment of COVID-19 Pandemic Outbreak.重新定位和传统药物治疗 COVID-19 大流行的最新方法。
Mini Rev Med Chem. 2021;21(8):952-968. doi: 10.2174/1389557520666201124141103.
10
Lack of Effectiveness of Repurposed Drugs for COVID-19 Treatment.用于治疗新冠病毒病的重新利用药物缺乏有效性。
Front Immunol. 2021 Mar 11;12:635371. doi: 10.3389/fimmu.2021.635371. eCollection 2021.

引用本文的文献

1
Comprehensive and translational pathobiology of COVID-19 based on cellular and molecular techniques.基于细胞和分子技术的新冠病毒综合与转化病理生物学
Pract Lab Med. 2025 Aug 11;46:e00497. doi: 10.1016/j.plabm.2025.e00497. eCollection 2025 Sep.
2
Challenges in natural product-based drug discovery assisted with -based methods.基于[具体方法]辅助的天然产物药物发现中的挑战。 (原文中“-based methods”处表述不完整,可能影响准确理解)
RSC Adv. 2023 Oct 30;13(45):31578-31594. doi: 10.1039/d3ra06831e. eCollection 2023 Oct 26.
3
Drug-Induced Acute Pancreatitis in Hospitalized COVID-19 Patients.住院COVID-19患者的药物性急性胰腺炎
Diagnostics (Basel). 2023 Apr 12;13(8):1398. doi: 10.3390/diagnostics13081398.
4
Emerging Treatment Approaches for COVID-19 Infection: A Critical Review.新型冠状病毒肺炎感染的新兴治疗方法:批判性综述
Curr Mol Med. 2024;24(4):435-448. doi: 10.2174/1566524023666230417112543.
5
An Overview of Repurposed Drugs for Potential COVID-19 Treatment.用于潜在COVID-19治疗的老药概述。
Antibiotics (Basel). 2022 Nov 22;11(12):1678. doi: 10.3390/antibiotics11121678.
6
Plant-derived immuno-adjuvants in vaccines formulation: a promising avenue for improving vaccines efficacy against SARS-CoV-2 virus.植物来源的免疫佐剂在疫苗配方中的应用:提高疫苗针对 SARS-CoV-2 病毒疗效的有前途途径。
Pharmacol Rep. 2022 Dec;74(6):1238-1254. doi: 10.1007/s43440-022-00418-4. Epub 2022 Sep 20.
7
In silico analysis of SARS-CoV-2 spike protein N501Y and N501T mutation effects on human ACE2 binding.基于 SARS-CoV-2 刺突蛋白 N501Y 和 N501T 突变对人 ACE2 结合影响的计算机分析。
J Mol Graph Model. 2022 Nov;116:108260. doi: 10.1016/j.jmgm.2022.108260. Epub 2022 Jul 1.
8
A Tale of Three Recent Pandemics: Influenza, HIV and SARS-CoV-2.近期三大疫情之故事:流感、艾滋病毒与新型冠状病毒2019
Front Microbiol. 2022 Jun 2;13:889643. doi: 10.3389/fmicb.2022.889643. eCollection 2022.
9
Human SARS-CoV-2 has evolved to increase U content and reduce genome size.人类 SARS-CoV-2 已经进化到增加 U 含量并减少基因组大小。
Int J Biol Macromol. 2022 Apr 15;204:356-363. doi: 10.1016/j.ijbiomac.2022.02.034. Epub 2022 Feb 8.
10
Two years of SARS-CoV-2 infection (2019-2021): structural biology, vaccination, and current global situation.新型冠状病毒2019-2021年两年感染情况:结构生物学、疫苗接种及当前全球形势
Egypt J Intern Med. 2022;34(1):5. doi: 10.1186/s43162-021-00092-7. Epub 2022 Jan 14.

本文引用的文献

1
In vitro screening of a FDA approved chemical library reveals potential inhibitors of SARS-CoV-2 replication.在体外筛选美国食品药品监督管理局批准的化学药物库时发现了一些可能抑制 SARS-CoV-2 复制的化合物。
Sci Rep. 2020 Aug 4;10(1):13093. doi: 10.1038/s41598-020-70143-6.
2
TMPRSS2 and furin are both essential for proteolytic activation of SARS-CoV-2 in human airway cells.TMPRSS2 和 furin 均是 SARS-CoV-2 在人呼吸道细胞中蛋白水解激活所必需的。
Life Sci Alliance. 2020 Jul 23;3(9). doi: 10.26508/lsa.202000786. Print 2020 Sep.
3
Association of Angiotensin-Converting Enzyme Inhibitor or Angiotensin Receptor Blocker Use With COVID-19 Diagnosis and Mortality.血管紧张素转化酶抑制剂或血管紧张素受体阻滞剂的使用与 COVID-19 诊断和死亡率的关系。
JAMA. 2020 Jul 14;324(2):168-177. doi: 10.1001/jama.2020.11301.
4
Coronavirus breakthrough: dexamethasone is first drug shown to save lives.冠状病毒研究突破:地塞米松是首个被证明能挽救生命的药物。
Nature. 2020 Jun;582(7813):469. doi: 10.1038/d41586-020-01824-5.
5
Macrolides and viral infections: focus on azithromycin in COVID-19 pathology.大环内酯类药物与病毒感染:聚焦 COVID-19 病理学中的阿奇霉素。
Int J Antimicrob Agents. 2020 Aug;56(2):106053. doi: 10.1016/j.ijantimicag.2020.106053. Epub 2020 Jun 10.
6
Effect of Convalescent Plasma Therapy on Time to Clinical Improvement in Patients With Severe and Life-threatening COVID-19: A Randomized Clinical Trial.恢复期血浆疗法对重症和危及生命的 COVID-19 患者临床改善时间的影响:一项随机临床试验。
JAMA. 2020 Aug 4;324(5):460-470. doi: 10.1001/jama.2020.10044.
7
A review on possible modes of action of chloroquine/hydroxychloroquine: repurposing against SAR-CoV-2 (COVID-19) pandemic.关于氯喹/羟氯喹可能作用模式的综述:重新用于对抗 SAR-CoV-2(COVID-19)大流行。
Int J Antimicrob Agents. 2020 Aug;56(2):106028. doi: 10.1016/j.ijantimicag.2020.106028. Epub 2020 May 22.
8
SARS-CoV-2 Receptor ACE2 Is an Interferon-Stimulated Gene in Human Airway Epithelial Cells and Is Detected in Specific Cell Subsets across Tissues.SARS-CoV-2 受体 ACE2 是人类气道上皮细胞中的一种干扰素刺激基因,可在组织中的特定细胞亚群中检测到。
Cell. 2020 May 28;181(5):1016-1035.e19. doi: 10.1016/j.cell.2020.04.035. Epub 2020 Apr 27.
9
Structural Basis for Potent Neutralization of Betacoronaviruses by Single-Domain Camelid Antibodies.结构基础为单域骆驼科抗体对β冠状病毒的强效中和作用。
Cell. 2020 May 28;181(5):1004-1015.e15. doi: 10.1016/j.cell.2020.04.031. Epub 2020 May 5.
10
Identification of Antiviral Drug Candidates against SARS-CoV-2 from FDA-Approved Drugs.从 FDA 批准药物中鉴定抗 SARS-CoV-2 的抗病毒候选药物。
Antimicrob Agents Chemother. 2020 Jun 23;64(7). doi: 10.1128/AAC.00819-20.

抗 SARS-CoV-2 药物:它们的作用机制我们了解多少?

Drugs against SARS-CoV-2: What do we know about their mode of action?

机构信息

Laboratoire AFMB, Aix Marseille Université, CNRS, UMR 7257, Marseille, France.

Beyond Humanity, Lyon, France.

出版信息

Rev Med Virol. 2020 Nov;30(6):1-10. doi: 10.1002/rmv.2143. Epub 2020 Aug 11.

DOI:10.1002/rmv.2143
PMID:32779326
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7435512/
Abstract

The health emergency caused by the recent Covid-19 pandemic highlights the need to identify effective treatments against the virus causing this disease (SARS-CoV-2). The first clinical trials have been testing repurposed drugs that show promising anti-SARS-CoV-2 effects in cultured cells. Although more than 2400 clinical trials are already under way, the actual number of tested compounds is still limited to approximately 20, alone or in combination. In addition, knowledge on their mode of action (MoA) is currently insufficient. Their first results reveal some inconsistencies and contradictory results and suggest that cohort size and quality of the control arm are two key issues for obtaining rigorous and conclusive results. Moreover, the observed discrepancies might also result from differences in the clinical inclusion criteria, including the possibility of early treatment that may be essential for therapy efficacy in patients with Covid-19. Importantly, efforts should also be made to test new compounds with a documented MoA against SARS-CoV-2 in clinical trials. Successful treatment will probably be based on multitherapies with antiviral compounds that target different steps of the virus life cycle. Moreover, a multidisciplinary approach that combines artificial intelligence, compound docking, and robust in vitro and in vivo assays will accelerate the development of new antiviral molecules. Finally, large retrospective studies on hospitalized patients are needed to evaluate the different treatments with robust statistical tools and to identify the best treatment for each Covid-19 stage. This review describes different candidate antiviral strategies for Covid-19, by focusing on their mechanism of action.

摘要

由近期 COVID-19 大流行引起的卫生紧急情况突出表明,有必要确定针对该疾病(SARS-CoV-2)的有效治疗方法。首批临床试验一直在测试重新利用的药物,这些药物在培养细胞中显示出有希望的抗 SARS-CoV-2 作用。尽管已经有超过 2400 项临床试验正在进行,但实际测试的化合物数量仍然限于约 20 种,单独或组合使用。此外,对其作用机制(MoA)的了解目前仍然不足。它们的初步结果揭示了一些不一致和矛盾的结果,并表明队列规模和对照组的质量是获得严格和结论性结果的两个关键问题。此外,观察到的差异也可能是由于临床纳入标准的差异造成的,包括早期治疗的可能性,这对 COVID-19 患者的治疗效果可能至关重要。重要的是,还应努力在临床试验中测试具有针对 SARS-CoV-2 的记录 MoA 的新化合物。成功的治疗可能基于多种抗病毒化合物的联合治疗,这些化合物针对病毒生命周期的不同步骤。此外,结合人工智能、化合物对接以及强大的体外和体内检测的多学科方法将加速新抗病毒分子的开发。最后,需要对住院患者进行大型回顾性研究,以使用强大的统计工具评估不同的治疗方法,并确定每种 COVID-19 阶段的最佳治疗方法。本文通过重点介绍其作用机制,描述了针对 COVID-19 的不同候选抗病毒策略。