Development of potent and effective SARS-CoV-2 main protease inhibitors based on maleimide analogs for the potential treatment of COVID-19

被引:4
作者
Biernacki, Karol [1 ]
Ciupak, Olga [1 ]
Dasko, Mateusz [2 ]
Rachon, Janusz [1 ]
Flis, Damian [3 ]
Budka, Justyna [3 ]
Inkielewicz-Stepniak, Iwona [3 ]
Czaja, Anna [4 ]
Rak, Janusz [4 ]
Demkowicz, Sebastian [1 ]
机构
[1] Gdansk Univ Technol, Dept Organ Chem, Gdansk, Poland
[2] Gdansk Univ Technol, Dept Inorgan Chem, Gdansk, Poland
[3] Med Univ Gdansk, Dept Pharmaceut Pathophysiol, Gdansk, Poland
[4] Univ Gdansk, Dept Phys Chem, Gdansk, Poland
关键词
Coronavirus SARS-CoV-2; SARS-CoV-2 main protease mpro inhibitors; maleimide derivatives; COVID-19;
D O I
10.1080/14756366.2023.2290910
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
In the present work, we report a new series of potent SARS-CoV-2 Main Protease (Mpro) inhibitors based on maleimide derivatives. The inhibitory activities were tested in an enzymatic assay using recombinant Mpro (3CL Protease from coronavirus SARS-CoV-2). Within the set of new Mpro inhibitors, 6e demonstrated the highest activity in the enzymatic assay with an IC50 value of 8.52 +/- 0.44 mu M. The IC50 value for Nirmatrelvir (PF-07321332, used as a reference) was 0.84 +/- 0.37 mu M. The cytotoxic properties were determined in the MTT assay using MRC-5 and HEK-293 cell lines. In the course of the investigation, we found that the newly obtained maleimide derivatives are not substantially cytotoxic (IC50 values for most compounds were above 200 mu M).
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页数:10
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