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Development of potent and effective SARS-CoV-2 main protease inhibitors based on maleimide analogs for the potential treatment of COVID-19.
Biernacki, Karol; Ciupak, Olga; Dasko, Mateusz; Rachon, Janusz; Flis, Damian; Budka, Justyna; Inkielewicz-Stepniak, Iwona; Czaja, Anna; Rak, Janusz; Demkowicz, Sebastian.
Afiliación
  • Biernacki K; Department of Organic Chemistry, Gdansk University of Technology, Gdansk, Poland.
  • Ciupak O; Department of Organic Chemistry, Gdansk University of Technology, Gdansk, Poland.
  • Dasko M; Department of Inorganic Chemistry, Gdansk University of Technology, Gdansk, Poland.
  • Rachon J; Department of Organic Chemistry, Gdansk University of Technology, Gdansk, Poland.
  • Flis D; Department of Pharmaceutical Pathophysiology, Medical University of Gdansk, Gdansk, Poland.
  • Budka J; Department of Pharmaceutical Pathophysiology, Medical University of Gdansk, Gdansk, Poland.
  • Inkielewicz-Stepniak I; Department of Pharmaceutical Pathophysiology, Medical University of Gdansk, Gdansk, Poland.
  • Czaja A; Department of Physical Chemistry, University of Gdansk, Gdansk, Poland.
  • Rak J; Department of Physical Chemistry, University of Gdansk, Gdansk, Poland.
  • Demkowicz S; Department of Organic Chemistry, Gdansk University of Technology, Gdansk, Poland.
J Enzyme Inhib Med Chem ; 39(1): 2290910, 2024 Dec.
Article en En | MEDLINE | ID: mdl-38093611
ABSTRACT
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 µM. The IC50 value for Nirmatrelvir (PF-07321332, used as a reference) was 0.84 ± 0.37 µM. 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 µM).
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: COVID-19 Límite: Humans Idioma: En Revista: J Enzyme Inhib Med Chem Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2024 Tipo del documento: Article País de afiliación: Polonia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: COVID-19 Límite: Humans Idioma: En Revista: J Enzyme Inhib Med Chem Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2024 Tipo del documento: Article País de afiliación: Polonia
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