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Anti-SARS-CoV-2 activity of small molecule inhibitors of cathepsin L
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Wen-wen ZHOU, Bao-qing YOU, Yi-fan ZHENG, Shu-yi SI, Yan LI*, Jing ZHANG*
Acta Pharmaceutica Sinica | 2024, 59(3) : 600 - 607
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Acta Pharmaceutica Sinica | 2024, 59(3): 600-607
Original Articles
Anti-SARS-CoV-2 activity of small molecule inhibitors of cathepsin L
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Wen-wen ZHOU, Bao-qing YOU, Yi-fan ZHENG, Shu-yi SI, Yan LI*, Jing ZHANG*
Affiliations
  • Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China
Published: 2024-03-12 doi: 10.16438/j.0513-4870.2023-1214
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The coronavirus disease 2019 (COVID-19) is an acute infectious disease caused by the new severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, which has led to serious worldwide economic burden. Due to the continuous emergence of variants, vaccines and monoclonal antibodies are only partial effective against infections caused by distinct strains of SARS-CoV-2. Therefore, it is still of great importance to call for the development of broad-spectrum and effective small molecule drugs to combat both current and future outbreaks triggered by SARS-CoV-2. Cathepsin L (CatL) cleaves the spike glycoprotein (S) of SARS-CoV-2, playing an indispensable role in enhancing virus entry into host cells. Therefore CatL is one of the ideal targets for the development of pan-coronavirus inhibitor-based drugs. In this study, a CatL enzyme inhibitor screening model was established based on fluorescein labeled substrate. Two CatL inhibitors IMB 6290 and IMB 8014 with low cytotoxicity were obtained through high-throughput screening, the half inhibition concentrations (IC50) of which were 11.53 ± 0.68 and 1.56 ± 1.10 μmol·L-1, respectively. SDS-PAGE and cell-cell fusion experiments confirmed that the compounds inhibited the hydrolysis of S protein by CatL in a concentration-dependent manner. Surface plasmon resonance (SPR) detection showed that both compounds exhibited moderate binding affinity with CatL. Molecular docking revealed the binding mode between the compound and the CatL active pocket. The pseudovirus experiment further confirmed the inhibitory effects of IMB 8014 on the S protein mediated entry process. In vitro pharmacokinetic evaluation indicated that the compounds had relatively good drug-likeness properties. Our research suggested that these two compounds have the potential to be further developed as antiviral drugs for COVID-19 treatment.

SARS-CoV-2  /  cathepsin L  /  antiviral drug  /  small molecule inhibitor  /  high throughput screening
Wen-wen ZHOU, Bao-qing YOU, Yi-fan ZHENG, Shu-yi SI, Yan LI, Jing ZHANG. Anti-SARS-CoV-2 activity of small molecule inhibitors of cathepsin L[J]. Acta Pharmaceutica Sinica, 2024 , 59 (3) : 600 -607 . DOI: 10.16438/j.0513-4870.2023-1214
Year 2024 volume 59 Issue 3
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Article Info
doi: 10.16438/j.0513-4870.2023-1214
  • Receive Date:2023-10-27
  • Online Date:2025-11-28
  • Published:2024-03-12
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  • Received:2023-10-27
  • Revised:2023-12-19
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    Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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