Are vanadium complexes druggable against the main protease M(pro) of SARS-CoV-2? – A computational approach

In silico techniques helped explore the binding capacities of the SARS-CoV-2 main protease (M(pro)) for a series of metalloorganic compounds. Along with small size vanadium complexes a vanadium-containing derivative of the peptide-like inhibitor N3 (N-[(5-methylisoxazol-3-yl)carbonyl]alanyl-l-valyl-...

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Detalles Bibliográficos
Autores principales: Scior, Thomas, Abdallah, Hassan H., Mustafa, Siti Fatimah Zaharah, Guevara-García, José Antonio, Rehder, Dieter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2021
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7875704/
https://www.ncbi.nlm.nih.gov/pubmed/33589845
http://dx.doi.org/10.1016/j.ica.2021.120287

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7875704/
https://www.ncbi.nlm.nih.gov/pubmed/33589845
http://dx.doi.org/10.1016/j.ica.2021.120287

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