| Literature DB >> 30512950 |
Valentina Noemi Madia1, Antonella Messore1, Luca Pescatori1, Francesco Saccoliti1, Valeria Tudino1, Alessandro De Leo1, Luigi Scipione1, Lucia Fiore2, Eric Rhoden3, Fabrizio Manetti4,5, M Steven Oberste3, Roberto Di Santo1, Roberta Costi1.
Abstract
The final stages of polio eradication are proving more difficult than the early phases, and the development of effective drugs and treatments is considered a priority; thus, the research is ongoing. A screening of our in-house chemical library against poliovirus Sabin strains led to the identification of compounds 5 and 6 as hits active at submicromolar concentrations. Derivatives of these compounds were synthesized as a preliminary structure-activity-relationship study. Among them, 7 and 11 were highly active against poliovirus Sabin 1-3. Compound 11 was also very potent against a large panel of wild and vaccine-derived polioviruses. Time-of-addition experiments suggest that 5 and 7 could be active at an early stage of viral replication, whereas 11 was active at same concentration at all stages of viral replication. A ligand-based approach was applied to find the common structural features shared by the new compounds and already-known poliovirus inhibitors.Entities:
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Year: 2018 PMID: 30512950 PMCID: PMC9169555 DOI: 10.1021/acs.jmedchem.8b01482
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 8.039