• 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

用于治疗新冠肺炎的蛋白酶抑制剂GC376:从猫传染性腹膜炎中吸取的经验教训。

Protease inhibitor GC376 for COVID-19: Lessons learned from feline infectious peritonitis.

作者信息

Sharun Khan, Tiwari Ruchi, Dhama Kuldeep

机构信息

Division of Surgery, ICAR-Indian Veterinary Research Institute, Izatnagar, Bareilly, 243 122, Uttar Pradesh, India.

Department of Veterinary Microbiology and Immunology, College of Veterinary Sciences, Uttar Pradesh Pandit Deen Dayal Upadhyaya Pashu Chikitsa Vigyan Vishwavidyalaya Evam Go Anusandhan Sansthan (DUVASU), Mathura, 281001, India.

出版信息

Ann Med Surg (Lond). 2020 Dec 28;61:122-125. doi: 10.1016/j.amsu.2020.12.030. eCollection 2021 Jan.

DOI:10.1016/j.amsu.2020.12.030
PMID:33456770
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7797473/
Abstract

The main protease (M) of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is an important therapeutic target as it plays a major role in the processing and maturation of the viral polyprotein. GC376 is a pre-clinical dipeptide-based protease inhibitor that has been previously used for managing feline infectious peritonitis virus (FIPV). Since both GC373 and GC376 have already been successfully used in treating animal coronavirus infection, they can be considered as strong drug candidates for COVID-19 in humans. GC376 is a broad-spectrum antiviral drug that inhibits M of several viruses, including the coronaviruses like feline coronavirus, porcine epidemic diarrhoea virus, severe acute respiratory syndrome coronavirus, Middle East respiratory syndrome coronavirus, ferret, and mink coronavirus. However, further studies should be conducted to evaluate the potency, efficacy, and safety of these broad-spectrum M inhibitors in patients with COVID-19. The lessons learned from the successful use of drug candidates for treating animal coronavirus infections will help us to develop framework for their use in human trials.

摘要

严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的主要蛋白酶(M)是一个重要的治疗靶点,因为它在病毒多聚蛋白的加工和成熟过程中起主要作用。GC376是一种临床前基于二肽的蛋白酶抑制剂,此前已用于治疗猫传染性腹膜炎病毒(FIPV)。由于GC373和GC376都已成功用于治疗动物冠状病毒感染,它们可被视为治疗人类COVID-19的有力候选药物。GC376是一种广谱抗病毒药物,可抑制多种病毒的M蛋白酶,包括猫冠状病毒、猪流行性腹泻病毒、严重急性呼吸综合征冠状病毒、中东呼吸综合征冠状病毒、雪貂冠状病毒和水貂冠状病毒等冠状病毒。然而,应进一步开展研究,以评估这些广谱M蛋白酶抑制剂在COVID-19患者中的效力、疗效和安全性。从成功使用候选药物治疗动物冠状病毒感染中吸取的经验教训将有助于我们制定其在人体试验中的使用框架。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ee9/7797473/a09d5fbcbd57/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ee9/7797473/741ffc210dc1/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ee9/7797473/a09d5fbcbd57/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ee9/7797473/741ffc210dc1/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ee9/7797473/a09d5fbcbd57/gr2.jpg

相似文献

1
Protease inhibitor GC376 for COVID-19: Lessons learned from feline infectious peritonitis.用于治疗新冠肺炎的蛋白酶抑制剂GC376:从猫传染性腹膜炎中吸取的经验教训。
Ann Med Surg (Lond). 2020 Dec 28;61:122-125. doi: 10.1016/j.amsu.2020.12.030. eCollection 2021 Jan.
2
Structural basis of SARS-CoV-2 main protease inhibition by a broad-spectrum anti-coronaviral drug.一种广谱抗冠状病毒药物对SARS-CoV-2主要蛋白酶的抑制作用的结构基础
Am J Cancer Res. 2020 Aug 1;10(8):2535-2545. eCollection 2020.
3
Crystallization of Feline Coronavirus M With GC376 Reveals Mechanism of Inhibition.猫冠状病毒M与GC376的结晶揭示了抑制机制。
Front Chem. 2022 Feb 24;10:852210. doi: 10.3389/fchem.2022.852210. eCollection 2022.
4
Adaptive Mutation in the Main Protease Cleavage Site of Feline Coronavirus Renders the Virus More Resistant to Main Protease Inhibitors.猫冠状病毒主要蛋白酶切割位点的适应性突变使病毒对主要蛋白酶抑制剂更具抗性。
J Virol. 2022 Sep 14;96(17):e0090722. doi: 10.1128/jvi.00907-22. Epub 2022 Aug 24.
5
Structural-based virtual screening and in vitro assays for small molecules inhibiting the feline coronavirus 3CL protease as a surrogate platform for coronaviruses.基于结构的虚拟筛选和小分子抑制猫冠状病毒 3CL 蛋白酶的体外检测,作为冠状病毒的替代平台。
Antiviral Res. 2020 Oct;182:104927. doi: 10.1016/j.antiviral.2020.104927. Epub 2020 Sep 7.
6
Crystal Structure of Feline Infectious Peritonitis Virus Main Protease in Complex with Synergetic Dual Inhibitors.猫传染性腹膜炎病毒主要蛋白酶与协同双抑制剂复合物的晶体结构
J Virol. 2015 Dec 9;90(4):1910-7. doi: 10.1128/JVI.02685-15. Print 2016 Feb 15.
7
Current status on treatment options for feline infectious peritonitis and SARS-CoV-2 positive cats.猫传染性腹膜炎和 SARS-CoV-2 阳性猫的治疗选择现状。
Vet Q. 2020 Dec;40(1):322-330. doi: 10.1080/01652176.2020.1845917.
8
Protease inhibitors broadly effective against feline, ferret and mink coronaviruses.广谱抗猫、雪貂和水貂冠状病毒的蛋白酶抑制剂。
Antiviral Res. 2018 Dec;160:79-86. doi: 10.1016/j.antiviral.2018.10.015. Epub 2018 Oct 19.
9
Broad-spectrum inhibitors against 3C-like proteases of feline coronaviruses and feline caliciviruses.针对猫冠状病毒和猫杯状病毒3C样蛋白酶的广谱抑制剂。
J Virol. 2015 May;89(9):4942-50. doi: 10.1128/JVI.03688-14. Epub 2015 Feb 18.
10
Current concepts in the development of therapeutics against human and animal coronavirus diseases by targeting NP.通过靶向核蛋白开发抗人类和动物冠状病毒疾病疗法的当前概念
Comput Struct Biotechnol J. 2021;19:1072-1080. doi: 10.1016/j.csbj.2021.01.032. Epub 2021 Jan 30.

引用本文的文献

1
A potential allosteric inhibitor of SARS-CoV-2 main protease (M) identified through metastable state analysis.通过亚稳态分析鉴定出的一种潜在的严重急性呼吸综合征冠状病毒2型主要蛋白酶(M)变构抑制剂。
Front Mol Biosci. 2024 Sep 6;11:1451280. doi: 10.3389/fmolb.2024.1451280. eCollection 2024.
2
A Gaussia luciferase reporter assay for the evaluation of coronavirus Nsp5/3CLpro activity.用于评估冠状病毒 Nsp5/3CLpro 活性的海肾荧光素酶报告基因检测法。
Sci Rep. 2024 Sep 5;14(1):20697. doi: 10.1038/s41598-024-71305-6.
3
Sulforaphane's Nuclear Factor Erythroid 2-Related Factor 2 (Nrf2)-Dependent and -Independent Mechanism of Anti-SARS-CoV-2 Activity.

本文引用的文献

1
Coronavirus Infection of the Central Nervous System: Animal Models in the Time of COVID-19.冠状病毒感染中枢神经系统:COVID-19时代的动物模型
Front Vet Sci. 2020 Oct 23;7:584673. doi: 10.3389/fvets.2020.584673. eCollection 2020.
2
Structure and inhibition of the SARS-CoV-2 main protease reveal strategy for developing dual inhibitors against M and cathepsin L.SARS-CoV-2 主要蛋白酶的结构和抑制作用揭示了开发针对 M 和组织蛋白酶 L 的双重抑制剂的策略。
Sci Adv. 2020 Dec 9;6(50). doi: 10.1126/sciadv.abe0751. Print 2020 Dec.
3
Current status on treatment options for feline infectious peritonitis and SARS-CoV-2 positive cats.
萝卜硫素抗SARS-CoV-2活性的核因子红细胞2相关因子2(Nrf2)依赖性和非依赖性机制。
J Respir Biol Transl Med. 2024 Sep;1(3). doi: 10.35534/jrbtm.2024.10010. Epub 2024 Jun 24.
4
Why Certain Repurposed Drugs Are Unlikely to Be Effective Antivirals to Treat SARS-CoV-2 Infections.为何某些重新利用的药物不太可能成为治疗新冠病毒感染的有效抗病毒药物。
Viruses. 2024 Apr 22;16(4):651. doi: 10.3390/v16040651.
5
Statine-based peptidomimetic compounds as inhibitors for SARS-CoV-2 main protease (SARS-CoV‑2 Mpro).基于他汀类药物的肽模拟化合物作为 SARS-CoV-2 主蛋白酶(SARS-CoV-2 Mpro)抑制剂。
Sci Rep. 2024 Apr 18;14(1):8991. doi: 10.1038/s41598-024-59442-4.
6
assessment of diterpenes as potential inhibitors of SARS-COV-2 main protease.评估二萜类化合物作为新型冠状病毒主要蛋白酶的潜在抑制剂
Future Virol. 2023 Apr;18(5):295-308. doi: 10.2217/fvl-2022-0163. Epub 2023 May 22.
7
Computational Screening Using a Combination of Ligand-Based Machine Learning and Molecular Docking Methods for the Repurposing of Antivirals Targeting the SARS-CoV-2 Main Protease.基于配体的机器学习和分子对接方法的组合进行计算筛选,以重新利用针对 SARS-CoV-2 主蛋白酶的抗病毒药物。
Daru. 2024 Jun;32(1):47-65. doi: 10.1007/s40199-023-00484-w. Epub 2023 Oct 31.
8
Targeting the PEDV 3CL protease for identification of small molecule inhibitors: an insight from virtual screening, ADMET prediction, molecular dynamics, free energy landscape, and binding energy calculations.靶向猪流行性腹泻病毒3C样蛋白酶以鉴定小分子抑制剂:来自虚拟筛选、ADMET预测、分子动力学、自由能景观和结合能计算的见解
J Biol Eng. 2023 Apr 18;17(1):29. doi: 10.1186/s13036-023-00342-y.
9
Potential Anti-SARS-CoV-2 Prodrugs Activated by Phosphorylation and Their Role in the Aged Population.潜在的通过磷酸化激活的抗 SARS-CoV-2 前药及其在老年人群体中的作用。
Molecules. 2023 Mar 2;28(5):2332. doi: 10.3390/molecules28052332.
10
and computational investigations of novel synthetic carboxamide-linked pyridopyrrolopyrimidines with potent activity as SARS-CoV-2-M inhibitors.新型合成羧酰胺连接的吡啶并吡咯并嘧啶作为SARS-CoV-2-M抑制剂的活性及计算研究
RSC Adv. 2022 Sep 22;12(41):26895-26907. doi: 10.1039/d2ra04015h. eCollection 2022 Sep 16.
猫传染性腹膜炎和 SARS-CoV-2 阳性猫的治疗选择现状。
Vet Q. 2020 Dec;40(1):322-330. doi: 10.1080/01652176.2020.1845917.
4
Feline infectious peritonitis (FIP) and coronavirus disease 19 (COVID-19): Are they similar?猫传染性腹膜炎 (FIP) 和新型冠状病毒病 19 (COVID-19):它们相似吗?
Transbound Emerg Dis. 2021 Jul;68(4):1786-1799. doi: 10.1111/tbed.13856. Epub 2020 Oct 20.
5
Structural basis of SARS-CoV-2 main protease inhibition by a broad-spectrum anti-coronaviral drug.一种广谱抗冠状病毒药物对SARS-CoV-2主要蛋白酶的抑制作用的结构基础
Am J Cancer Res. 2020 Aug 1;10(8):2535-2545. eCollection 2020.
6
Both Boceprevir and GC376 efficaciously inhibit SARS-CoV-2 by targeting its main protease.博赛泼维与 GC376 均可通过靶向作用于 SARS-CoV-2 的主蛋白酶而有效抑制该病毒。
Nat Commun. 2020 Sep 4;11(1):4417. doi: 10.1038/s41467-020-18233-x.
7
Feline coronavirus drug inhibits the main protease of SARS-CoV-2 and blocks virus replication.猫冠状病毒药物可抑制新型冠状病毒的主要蛋白酶并阻断病毒复制。
Nat Commun. 2020 Aug 27;11(1):4282. doi: 10.1038/s41467-020-18096-2.
8
3C-like protease inhibitors block coronavirus replication in vitro and improve survival in MERS-CoV-infected mice.3C 样蛋白酶抑制剂可阻断冠状病毒在体外的复制,并改善 MERS-CoV 感染小鼠的存活率。
Sci Transl Med. 2020 Aug 19;12(557). doi: 10.1126/scitranslmed.abc5332. Epub 2020 Aug 3.
9
Coronavirus Disease 2019-COVID-19.新型冠状病毒肺炎。
Clin Microbiol Rev. 2020 Jun 24;33(4). doi: 10.1128/CMR.00028-20. Print 2020 Sep 16.
10
Boceprevir, GC-376, and calpain inhibitors II, XII inhibit SARS-CoV-2 viral replication by targeting the viral main protease.博赛匹韦、GC-376 和钙蛋白酶抑制剂 II、XII 通过靶向病毒主蛋白酶抑制 SARS-CoV-2 病毒复制。
Cell Res. 2020 Aug;30(8):678-692. doi: 10.1038/s41422-020-0356-z. Epub 2020 Jun 15.