Detalle de: Discovery of Thiophene Derivatives as Potent, Orally Bioavailable, and Blood–Brain Barrier-Permeable Ebola Virus Entry Inhibitors
| Title | Discovery of Thiophene Derivatives as Potent, Orally Bioavailable, and Blood–Brain Barrier-Permeable Ebola Virus Entry Inhibitors |
| Abstract |
The endemic nature of the Ebola virus disease in Africa underscores the need for prophylactic and therapeutic drugs that are affordable and easy to administer. Through a phenotypic screening employing viral pseudotypes and our in-house chemical library, we identified a promising hit featuring a thiophene scaffold, exhibiting antiviral activity in the micromolar range. Following up on this thiophene hit, a new series of compounds that retain the five-membered heterocyclic scaffold while modifying several substituents was synthesized. Initial screening using a pseudotype viral system and validation assays employing authentic Ebola virus demonstrated the potential of this new chemical class as viral entry inhibitors. Subsequent investigations elucidated the mechanism of action through site-directed mutagenesis. Furthermore, we conducted studies to assess the pharmacokinetic profile of selected compounds to confirm its pharmacological and therapeutic potential. |
| Apa Reference | Morales-Tenorio, M., Lasala, F., Garcia-Rubia, A., Aledavood, E., Heung, M., Olal, C., Escudero-Pérez, B., Alonso, C., Martínez, A., Muñoz-Fontela, C., Delgado, R., & Gil, C. (2024). Discovery of Thiophene Derivatives as Potent, Orally Bioavailable, and Blood–Brain Barrier-Permeable Ebola Virus Entry Inhibitors. Journal of Medicinal Chemistry, 67(18), 16381–16402. 10.1021/acs.jmedchem.4c01267 |
| Doi | 10.1021/acs.jmedchem.4c01267 |
| Publication Date | 9 Sep 2024 |
| Publication Type | Article |
| Researcher | Ana Martínez |
| Ontology | Genome Assembly, Mutation Analysis and design, Structure-function relationship, Drug Discovery and design |
| Research Groups | Translational Medicinal and Biological Chemistry |
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