SARS-CoV-2 main protease inhibitors: What is moving in the field of peptides and peptidomimetics?

被引:4
作者
Algar-Lizana, Sergio [1 ]
Angeles Bonache, Maria [1 ]
Gonzalez-Muniz, Rosario [1 ]
机构
[1] Inst Quim Med IQM CSIC, Dept Biomimet, Juan Cierva 3, Madrid 28006, Spain
关键词
covalent; COVID-19; inhibitors; main protease; Mpro; peptides; peptidomimetics; SARS-CoV-2; DESIGN; MECHANISM;
D O I
10.1002/psc.3467
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The COVID-19 pandemic, caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is still affecting people worldwide. Despite the good degree of immunological protection achieved through vaccination, there are still severe cases that require effective antivirals. In this sense, two specific pharmaceutical preparations have been marketed already, the RdRp polymerase inhibitor molnupiravir and the main viral protease inhibitor nirmatrelvir (commercialized as Paxlovid, a combination with ritonavir). Nirmatrelvir is a peptidomimetic acting as orally available, covalent, and reversible inhibitor of SARS-CoV-2 main viral protease. The success of this compound has revitalized the search for new peptide and peptidomimetic protease inhibitors. This highlight collects some selected examples among those recently published in the field of SARS-CoV-2.
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页数:6
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共 54 条
[1]   Advances in the Development of SARS-CoV-2 Mpro Inhibitors [J].
Agost-Beltran, Laura ;
de la Hoz-Rodriguez, Sergio ;
Bou-Iserte, Lledo ;
Rodriguez, Santiago ;
Fernandez-de-la-Pradilla, Adrian ;
Gonzalez, Florenci V. .
MOLECULES, 2022, 27 (08)
[2]  
Alugubelli Yugendar R, 2021, bioRxiv, DOI 10.1101/2021.12.18.473330
[3]   Building on Success: A Bright Future for Peptide Therapeutics [J].
Angell, Yvonne ;
Holford, Mande ;
Moos, Walter H. .
PROTEIN AND PEPTIDE LETTERS, 2018, 25 (12) :1044-1050
[4]  
[Anonymous], 2020, Biochemistry, DOI DOI 10.1101/2020.10.29.339317
[5]  
[Anonymous], EURPEPSOCCOMSMALL PE
[6]  
[Anonymous], LIST CRITICAL MED CO
[7]   Mechanism of inhibition of SARS-CoV-2 Mpro by N3 peptidyl Michael acceptor explained by QM/MM simulations and design of new derivatives with tunable chemical reactivity [J].
Arafet, Kemel ;
Serrano-Aparicio, Natalia ;
Lodola, Alessio ;
Mulholland, Adrian J. ;
Gonzalez, Florenci, V ;
Swiderek, Katarzyna ;
Moliner, Vicent .
CHEMICAL SCIENCE, 2021, 12 (04) :1433-1444
[8]   Peptidomimetic α-Acyloxymethylketone Warheads with Six-Membered Lactam P1 Glutamine Mimic: SARS-CoV-2 3CL Protease Inhibition, Coronavirus Antiviral Activity, and in Vitro Biological Stability [J].
Bai, Bing ;
Belovodskiy, Alexandr ;
Hena, Mostofa ;
Kandadai, Appan Srinivas ;
Joyce, Michael A. ;
Saffran, Holly A. ;
Shields, Justin A. ;
Khan, Muhammad Bashir ;
Arutyunova, Elena ;
Lu, Jimmy ;
Bajwa, Sardeev K. ;
Hockman, Darren ;
Fischer, Conrad ;
Lamer, Tess ;
Vuong, Wayne ;
van Belkum, Marco J. ;
Gu, Zhengxian ;
Lin, Fusen ;
Du, Yanhua ;
Xu, Jia ;
Rahim, Mohammad ;
Young, Howard S. ;
Vederas, John C. ;
Tyrrell, D. Lorne ;
Lemieux, M. Joanne ;
Nieman, James A. .
JOURNAL OF MEDICINAL CHEMISTRY, 2022, 65 (04) :2905-2925
[9]  
Boras Britton, 2021, bioRxiv, DOI 10.1101/2020.09.12.293498
[10]   Evaluation of SARS-CoV-2 Main Protease Inhibitors Using a Novel Cell-Based Assay [J].
Cao, Wenyue ;
Cho, Chia-Chuan Dean ;
Geng, Zhi Zachary ;
Shaabani, Namir ;
Ma, Xinyu R. ;
Vatansever, Erol C. ;
Alugubelli, Yugendar R. ;
Ma, Yuying ;
Chaki, Sankar P. ;
Ellenburg, William H. ;
Yang, Kai S. ;
Qiao, Yuchen ;
Allen, Robert ;
Neuman, Benjamin W. ;
Ji, Henry ;
Xu, Shiqing ;
Liu, Wenshe Ray .
ACS CENTRAL SCIENCE, 2022, 8 (02) :192-204