Progress on SARS-CoV-2 3CLpro Inhibitors: Inspiration from SARS-CoV 3CLpro Peptidomimetics and Small-Molecule Anti-Inflammatory Compounds

被引:31
|
作者
Zhu, Jiajie [1 ]
Zhang, Haiyan [2 ]
Lin, Qinghong [1 ]
Lyu, Jingting [1 ]
Lu, Lu [1 ]
Chen, Hanxi [1 ]
Zhang, Xuning [1 ]
Zhang, Yanjun [3 ]
Chen, Keda [1 ]
机构
[1] Zhejiang Shuren Univ, Shulan Int Med Coll, Hangzhou, Peoples R China
[2] Zhejiang Chinese Med Univ, Hangzhou, Peoples R China
[3] Zhejiang Prov Ctr Dis Control & Prevent, Hangzhou, Peoples R China
来源
DRUG DESIGN DEVELOPMENT AND THERAPY | 2022年 / 16卷
关键词
SARS-CoV; SARS-CoV-2; 3CLpro; peptidomimetics; anti-inflammatory agents; small-molecule inhibitors; protease; inhibitors; CORONAVIRUS 3C-LIKE PROTEASE; MAIN PROTEASE; CRYSTAL-STRUCTURE; DIMER INTERFACE; PROTEINASE; MECHANISM; DESIGN; DISSOCIATION; DIMERIZATION; FLAVONOIDS;
D O I
10.2147/DDDT.S359009
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) currently poses a threat to human health. 3C-like proteinase (3CLpro) plays an important role in the viral life cycle. Hence, it is considered an attractive antiviral target protein. Whole-genome sequencing showed that the sequence homology between SARS-CoV-2 3CLpro and SARS-CoV 3CLpro is 96.08%, with high similarity in the substrate-binding region. Thus, assessing peptidomimetic inhibitors of SARS-CoV 3CLpro could accelerate the development of peptidomimetic inhibitors for SARS-CoV-2 3CLpro. Accordingly, we herein discuss progress on SARS-CoV-2 3CLpro peptidomimetic inhibitors. Inflammation plays a major role in the pathophysiological process of COVID-19. Small-molecule compounds targeting 3CLpro with both antiviral and anti-inflammatory effects are also briefly discussed in this paper.
引用
收藏
页码:1067 / 1082
页数:16
相关论文
共 50 条
  • [21] Structural and functional characterization of NEMO cleavage by SARS-CoV-2 3CLpro
    Hameedi, Mikhail Ali
    Prates, Erica T.
    Garvin, Michael R.
    Mathews, Irimpan
    Amos, B. Kirtley
    Demerdash, Omar
    Bechthold, Mark
    Iyer, Mamta
    Rahighi, Simin
    Kneller, Daniel W.
    Kovalevsky, Andrey
    Irle, Stephan
    Van-Quan Vuong
    Mitchell, Julie C.
    Labbe, Audrey
    Galanie, Stephanie
    Wakatsuki, Soichi
    Jacobson, Daniel
    NATURE COMMUNICATIONS, 2022, 13 (01)
  • [22] Human Superantibodies to 3CLpro Inhibit Replication of SARS-CoV-2 across Variants
    Glab-ampai, Kittirat
    Kaewchim, Kanasap
    Saenlom, Thanatsaran
    Thepsawat, Watayagorn
    Mahasongkram, Kodchakorn
    Sookrung, Nitat
    Chaicumpa, Wanpen
    Chulanetra, Monrat
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (12)
  • [23] Flavonoids from Siparuna cristata inhibitors against SARS-Cov-2 3Clpro? An in silico investigation
    Esteves, Maria Eduarda Alves
    Leal, Carla Monteiro
    Leitao, Suzana Guimaraes
    Leitao, Gilda Guimaraes
    da Silva, Manuela Leal
    BIOPHYSICAL REVIEWS, 2021, 13 (06) : 1454 - 1454
  • [24] A Study of Drug Repurposing to Identify SARS-CoV-2 Main Protease (3CLpro) Inhibitors
    Jo, Seri
    Signorile, Luca
    Kim, Suwon
    Kim, Mi-Sun
    Huertas, Oscar
    Insa, Raul
    Reig, Nuria
    Shin, Dong Hae
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (12)
  • [25] Molecular Docking Studies on the Anti-viral Effects of Compounds From Kabasura Kudineer on SARS-CoV-2 3CLpro
    Vincent, Savariar
    Arokiyaraj, Selvaraj
    Saravanan, Muthupandian
    Dhanraj, Manoj
    FRONTIERS IN MOLECULAR BIOSCIENCES, 2020, 7
  • [26] SARS-CoV 3CLpro inhibitory effects of quinone-methide triterpenes from Tripterygium regelii
    Ryu, Young Bae
    Park, Su-Jin
    Kim, Young Min
    Lee, Ju-Yeon
    Seo, Woo Duck
    Chang, Jong Sun
    Park, Ki Hun
    Rho, Mun-Chual
    Lee, Woo Song
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2010, 20 (06) : 1873 - 1876
  • [27] Structure-based design,synthesis, and biological evaluation of peptidomimetic SARS-CoV 3CLpro inhibitors
    Ghosh, Arun K.
    Xi, Kai
    Grum-Tokars, Valerie
    Xu, Xiaoming
    Ratia, Kiira
    Fu, Wentao
    Houser, Katherine V.
    Baker, Susan C.
    Johnson, Michael E.
    Mesecar, Andrew D.
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2007, 17 (21) : 5876 - 5880
  • [28] Structural stability of SARS-CoV-2 3CLpro and identification of quercetin as an inhibitor by experimental screening
    Abian, Olga
    Ortega-Alarcon, David
    Jimenez-Alesanco, Ana
    Ceballos-Laita, Laura
    Vega, Sonia
    Reyburn, Hugh T.
    Rizzuti, Bruno
    Velazquez-Campoy, Adrian
    INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2020, 164 : 1693 - 1703
  • [29] Targeting 3CLpro and SARS-CoV-2 RdRp by Amphimedon sp. Metabolites: A Computational Study
    Shady, Nourhan Hisham
    Hayallah, Alaa M.
    Mohamed, Mamdouh F. A.
    Ghoneim, Mohammed M.
    Chilingaryan, Garri
    Al-Sanea, Mohammad M.
    Fouad, Mostafa A.
    Kamel, Mohamed Salah
    Abdelmohsen, Usama Ramadan
    MOLECULES, 2021, 26 (12):
  • [30] Repositioning therapeutics for COVID-19: virtual screening of the potent synthetic and natural compounds as SARS-CoV-2 3CLpro inhibitors
    Sattari, Ahmad
    Ramazani, Ali
    Aghahosseini, Hamideh
    JOURNAL OF THE IRANIAN CHEMICAL SOCIETY, 2021, 18 (10) : 2807 - 2827