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Design, Synthesis and Discovery of N,N’‐Carbazoyl‐aryl‐urea Inhibitors of Zika NS5 Methyltransferase and Virus Replication

The recent outbreaks of Zika virus (ZIKV) infection worldwide make the discovery of novel antivirals against flaviviruses a research priority. This work describes the identification of novel inhibitors of ZIKV through a structure‐based virtual screening approach using the ZIKV NS5‐MTase. A novel ser...

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Detalles Bibliográficos
Autores principales: Spizzichino, Sharon, Mattedi, Giulio, Lauder, Kate, Valle, Coralie, Aouadi, Wahiba, Canard, Bruno, Decroly, Etienne, Kaptein, Suzanne J. F., Neyts, Johan, Graham, Carl, Sule, Zakary, Barlow, David J., Silvestri, Romano, Castagnolo, Daniele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7106487/
https://www.ncbi.nlm.nih.gov/pubmed/31805205
http://dx.doi.org/10.1002/cmdc.201900533
Descripción
Sumario:The recent outbreaks of Zika virus (ZIKV) infection worldwide make the discovery of novel antivirals against flaviviruses a research priority. This work describes the identification of novel inhibitors of ZIKV through a structure‐based virtual screening approach using the ZIKV NS5‐MTase. A novel series of molecules with a carbazoyl‐aryl‐urea structure has been discovered and a library of analogues has been synthesized. The new compounds inhibit ZIKV MTase with IC(50) between 23–48 μM. In addition, carbazoyl‐aryl‐ureas also proved to inhibit ZIKV replication activity at micromolar concentration.