Bench-to-bedside: Innovation of small molecule anti-SARS-CoV-2 drugs in China

被引:66
作者
Yang, Liyan [1 ,2 ]
Wang, Zhonglei [3 ,4 ]
机构
[1] Qufu Normal Univ, Sch Phys & Phys Engn, Qufu 273165, Peoples R China
[2] Chinese Acad Sci, Inst Chem, Beijing Natl Lab Mol Sci, Beijing 100190, Peoples R China
[3] Qufu Normal Univ, Key Lab Green Nat Prod & Pharmaceut Intermediates, Sch Chem & Chem Engn, Qufu 273165, Peoples R China
[4] Tsinghua Univ, Sch Pharmaceut Sci, Key Lab Bioorgan Phosphorus Chem & Chem Biol, Minist Educ, Beijing 100084, Peoples R China
关键词
COVID-19; SARS-CoV-2; Azvudine; VV116; FB2001; Cepharanthine; C VIRUS-REPLICATION; MAIN PROTEASE INHIBITORS; ANTIVIRAL ACTIVITY; EBOLA-VIRUS; COVALENT INHIBITORS; NUCLEOSIDE ANALOGS; SARS-COV-2; DISCOVERY; DESIGN; 4'-AZIDOCYTIDINE;
D O I
10.1016/j.ejmech.2023.115503
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The ongoing COVID-19 pandemic has resulted in millions of deaths globally, highlighting the need to develop potent prophylactic and therapeutic strategies against SARS-CoV-2. Small molecule inhibitors (remdesivir, Paxlovid, and molnupiravir) are essential complements to vaccines and play important roles in clinical treatment of SARS-CoV-2. Many advances have been made in development of anti-SARS-CoV-2 inhibitors in China, but progress in discovery and characterization of pharmacological activity, antiviral mechanisms, and clinical effi-cacy are limited. We review development of small molecule anti-SARS-CoV-2 drugs (azvudine [approved by the NMPA of China on July 25, 2022], VV116 [approved by the NMPA of China on January 29, 2023], FB2001, WPV01, pentarlandir, and cepharanthine) in China and summarize their pharmacological activity, potential mechanisms of action, clinical trials and use, and important milestones in their discovery. The role of structural biology in drug development is also reviewed. Future studies should focus on development of diverse second-generation inhibitors with excellent oral bioavailability, superior plasma half-life, increased antiviral activity against SARS-CoV-2 and its variants, high target specificity, minimal side effects, reduced drug-drug interactions, and improved lung histopathology.
引用
收藏
页数:15
相关论文
共 163 条
[1]   Remdesivir plus standard of care versus standard of care alone for the treatment of patients admitted to hospital with COVID-19 (DisCoVeRy): a phase 3, randomised, controlled, open-label trial [J].
Ader, Florence ;
Bouscambert-Duchamp, Maude ;
Hites, Maya ;
Peiffer-Smadja, Nathan ;
Poissy, Julien ;
Belhadi, Drifa ;
Diallo, Alpha ;
Le, Minh-Patrick ;
Peytavin, Gilles ;
Staub, Therese ;
Greil, Richard ;
Guedj, Jeremie ;
Paiva, Jose-Artur ;
Costagliola, Dominique ;
Yazdanpanah, Yazdan ;
Burdet, Charles ;
Mentre, France .
LANCET INFECTIOUS DISEASES, 2022, 22 (02) :209-221
[2]   SARS-CoV-2 Omicron BA.5: Evolving tropism and evasion of potent humoral responses and resistance to clinical immunotherapeutics relative to viral variants of concern [J].
Aggarwal, Anupriya ;
Akerman, Anouschka ;
Milogiannakis, Vanessa ;
Silva, Mariana Ruiz ;
Walker, Gregory ;
Stella, Alberto Ospina ;
Kindinger, Andrea ;
Angelovich, Thomas ;
Waring, Emily ;
Amatayakul-Chantler, Supavadee ;
Roth, Nathan ;
Manni, Sandro ;
Hauser, Thomas ;
Barnes, Thomas ;
Condylios, Anna ;
Yeang, Malinna ;
Wong, Maureen ;
Jean, Tyra ;
Foster, Charles S. P. ;
Christ, Daniel ;
Hoppe, Alexandra Carey ;
Munier, Mee Ling ;
Darley, David ;
Churchill, Melissa ;
Stark, Damien J. ;
Matthews, Gail ;
Rawlinson, William D. ;
Kelleher, Anthony D. ;
Turville, Stuart G. .
EBIOMEDICINE, 2022, 84
[3]  
ANZAI K, 1957, J ANTIBIOT, V10, P201
[4]   Nirmatrelvir Use and Severe Covid-19 Outcomes during the Omicron Surge [J].
Arbel, Ronen ;
Sagy, Yael Wolff ;
Hoshen, Moshe ;
Battat, Erez ;
Lavie, Gil ;
Sergienko, Ruslan ;
Friger, Michael ;
Waxman, Jacob G. ;
Dagan, Noa ;
Balicer, Ran ;
Ben-Shlomo, Yatir ;
Peretz, Alon ;
Yaron, Shlomit ;
Serby, Danielle ;
Hammerman, Ariel ;
Netzer, Doron .
NEW ENGLAND JOURNAL OF MEDICINE, 2022, 387 (09) :790-798
[5]   Potent Anti-SARS-CoV-2 Activity by the Natural Product Gallinamide A and Analogues via Inhibition of Cathepsin L [J].
Ashhurst, Anneliese S. ;
Tang, Arthur H. ;
Fajtova, Pavla ;
Yoon, Michael C. ;
Aggarwal, Anupriya ;
Bedding, Max J. ;
Stoye, Alexander ;
Beretta, Laura ;
Pwee, Dustin ;
Drelich, Aleksandra ;
Skinner, Danielle ;
Li, Linfeng ;
Meek, Thomas D. ;
McKerrow, James H. ;
Hook, Vivian ;
Tseng, Chien-Te ;
Larance, Mark ;
Turville, Stuart ;
Gerwick, William H. ;
O'Donoghue, Anthony J. ;
Payne, Richard J. .
JOURNAL OF MEDICINAL CHEMISTRY, 2022, 65 (04) :2956-2970
[6]   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
[7]   Cepharanthine: An update of its mode of action, pharmacological properties and medical applications [J].
Bailly, Christian .
PHYTOMEDICINE, 2019, 62
[8]   Preclinical characterization of an intravenous coronavirus 3CL protease inhibitor for the potential treatment of COVID19 [J].
Boras, Britton ;
Jones, Rhys M. ;
Anson, Brandon J. ;
Arenson, Dan ;
Aschenbrenner, Lisa ;
Bakowski, Malina A. ;
Beutler, Nathan ;
Binder, Joseph ;
Chen, Emily ;
Eng, Heather ;
Hammond, Holly ;
Hammond, Jennifer ;
Haupt, Robert E. ;
Hoffman, Robert ;
Kadar, Eugene P. ;
Kania, Rob ;
Kimoto, Emi ;
Kirkpatrick, Melanie G. ;
Lanyon, Lorraine ;
Lendy, Emma K. ;
Lillis, Jonathan R. ;
Logue, James ;
Luthra, Suman A. ;
Ma, Chunlong ;
Mason, Stephen W. ;
McGrath, Marisa E. ;
Noell, Stephen ;
Obach, R. Scott ;
O' Brien, Matthew N. ;
O'Connor, Rebecca ;
Ogilvie, Kevin ;
Owen, Dafydd ;
Pettersson, Martin ;
Reese, Matthew R. ;
Rogers, Thomas F. ;
Rosales, Romel ;
Rossulek, Michelle I. ;
Sathish, Jean G. ;
Shirai, Norimitsu ;
Steppan, Claire ;
Ticehurst, Martyn ;
Updyke, Lawrence W. ;
Weston, Stuart ;
Zhu, Yuao ;
White, Kris M. ;
Garcia-Sastre, Adolfo ;
Wang, Jun ;
Chatterjee, Arnab K. ;
Mesecar, Andrew D. ;
Frieman, Matthew B. .
NATURE COMMUNICATIONS, 2021, 12 (01)
[9]   SARS-CoV-2: from its discovery to genome structure, transcription, and replication [J].
Brant, Ayslan Castro ;
Tian, Wei ;
Majerciak, Vladimir ;
Yang, Wei ;
Zheng, Zhi-Ming .
CELL AND BIOSCIENCE, 2021, 11 (01)
[10]   FXR inhibition may protect from SARS-CoV-2 infection by reducing ACE2 [J].
Brevini, Teresa ;
Maes, Mailis ;
Webb, Gwilym J. ;
John, Binu, V ;
Fuchs, Claudia D. ;
Buescher, Gustav ;
Wang, Lu ;
Griffiths, Chelsea ;
Brown, Marnie L. ;
Scott, William E., III ;
Pereyra-Gerber, Pehuen ;
Gelson, William T. H. ;
Brown, Stephanie ;
Dillon, Scott ;
Muraro, Daniele ;
Sharp, Jo ;
Neary, Megan ;
Box, Helen ;
Tatham, Lee ;
Stewart, James ;
Curley, Paul ;
Pertinez, Henry ;
Forrest, Sally ;
Mlcochova, Petra ;
Varankar, Sagar S. ;
Darvish-Damavandi, Mahnaz ;
Mulcahy, Victoria L. ;
Kuc, Rhoda E. ;
Williams, Thomas L. ;
Heslop, James A. ;
Rossetti, Davide ;
Tysoe, Olivia C. ;
Galanakis, Vasileios ;
Vila-Gonzalez, Marta ;
Crozier, Thomas W. M. ;
Bargehr, Johannes ;
Sinha, Sanjay ;
Upponi, Sara S. ;
Fear, Corrina ;
Swift, Lisa ;
Saeb-Parsy, Kourosh ;
Davies, Susan E. ;
Wester, Axel ;
Hagstrom, Hannes ;
Melum, Espen ;
Clements, Darran ;
Humphreys, Peter ;
Herriott, Jo ;
Kijak, Edyta ;
Cox, Helen .
NATURE, 2023, 615 (7950) :134-+