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Detalle de: N'-Phenylacetohydrazide Derivatives as Potent Ebola Virus Entry Inhibitors with an Improved Pharmacokinetic Profile

Title N'-Phenylacetohydrazide Derivatives as Potent Ebola Virus Entry Inhibitors with an Improved Pharmacokinetic Profile
Abstract

Ebola virus (EBOV) is a single-strand RNA virus belonging to the Filoviridae family, which has been associated to most Ebola virus disease outbreaks to date, including the West African and the North Kivu epidemics between 2013 and 2022. This unprecedented health emergency prompted the search for effective medical countermeasures. Following up on the carbazole hit identified in our previous studies, we synthetized a new series of compounds, which demonstrated to prevent EBOV infection in cells by acting as virus entry inhibitors. The in vitro inhibitory activity was evaluated through the screening against surrogate models based on viral pseudotypes and further confirmed using replicative EBOV. Docking and molecular dynamics simulations joined to saturation transfer difference-nuclear magnetic resonance (STD-NMR) and mutagenesis experiments to elucidate the biological target of the most potent compounds. Finally, in vitro metabolic stability and in vivo pharmacokinetic studies were performed to confirm their therapeutic potential.

Apa Reference Garcia-Rubia, A., Lasala, F., Ginex, T., Morales-Tenorio, M., Olal, C., Heung, M., Oquist, P., Galindo, I., Cuesta-Geijo, M. Á., Casasnovas, J. M., Campillo, N. E., Canales, Á., Alonso, C., Martínez, A., Muñoz-Fontela, C., Delgado, R., & Gil, C. (2023). N′-Phenylacetohydrazide Derivatives as Potent Ebola Virus Entry Inhibitors with an Improved Pharmacokinetic Profile. Journal of Medicinal Chemistry, 66(8), 5465–5483. 10.1021/acs.jmedchem.2c01785
Doi 10.1021/acs.jmedchem.2c01785
Publication Date 6 Apr 2023
Publication Type Article
Researcher Ana Martínez
Ontology Computational models and simulations, Mutation Analysis and design, Biomolecular simulation, Drug Discovery and design, Molecular Interactions/Docking
Research Groups Translational Medicinal and Biological Chemistry
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