| Literature DB >> 32435411 |
Annalaura Brai1, Adele Boccuto2, Martina Monti3, Serena Marchi3, Ilaria Vicenti2, Francesco Saladini2, Claudia Immacolata Trivisani1, Alessandro Pollutri1, Claudia Maria Trombetta3, Emanuele Montomoli3,4, Valentina Riva5, Anna Garbelli5, Emanuele Maria Nola5, Maurizio Zazzi2, Giovanni Maga5, Elena Dreassi1, Maurizio Botta1,6.
Abstract
In the absence of effective drugs or vaccines for the treatment of the five Dengue Virus serotypes, the search for novel antiviral drugs is of primary importance for the scientific community. In this context, drug repurposing represents the most used strategy; however, the study of host targets is now attracting attention since it allows identification of broad-spectrum drugs endowed with high genetic barrier. In the last ten years our research group identified several small molecules DDX3X inhibitors and proved their efficacy against different viruses including novel emerging ones. Herein, starting from a screening of our compounds, we designed and synthesized novel derivatives with potent activity and high selectivity. Finally, we synthesized a fluorescent inhibitor that allowed us to study DDX3X cellular localization during DENV infection in vitro. Immunofluorescence analysis showed that our inhibitor colocalized with DDX3X, promoting the reduction of infected cells and recovering the number of viable cells.Entities:
Year: 2020 PMID: 32435411 PMCID: PMC7236276 DOI: 10.1021/acsmedchemlett.9b00681
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345