Journal article 619 views 82 downloads
Rational design of novel nucleoside analogues reveals potent antiviral agents for EV71
European Journal of Medicinal Chemistry, Volume: 246, Start page: 114942
Swansea University Authors: Martina Salerno Salerno, Salvatore Ferla , Marcella Bassetto
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DOI (Published version): 10.1016/j.ejmech.2022.114942
Abstract
Different viruses belonging to distinct viral families, such as enterovirus 71, rely on the host methyltransferase METTL3 for the completion of fundamental cytoplasmic stages of their life cycle. Modulation of the activity of this enzyme could therefore provide a broad-spectrum approach to interfere...
Published in: | European Journal of Medicinal Chemistry |
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ISSN: | 0223-5234 |
Published: |
Elsevier BV
2023
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Online Access: |
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URI: | https://cronfa.swan.ac.uk/Record/cronfa62048 |
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Abstract: |
Different viruses belonging to distinct viral families, such as enterovirus 71, rely on the host methyltransferase METTL3 for the completion of fundamental cytoplasmic stages of their life cycle. Modulation of the activity of this enzyme could therefore provide a broad-spectrum approach to interfere with viral infections caused by viruses that depend on its activity for the completion of their viral cycle. With the aim to identify antiviral therapeutics with this effect, a series of new nucleoside analogues was rationally designed to act as inhibitors of human METTL3, as a novel approach to interfere with a range of viral infections. Guided by molecular docking studies on the SAM binding pocket of the enzyme, 24 compounds were prepared following multiple-step synthetic protocols, and evaluated for their ability to interfere with the replication of different viruses in cell-based systems, and to directly inhibit the activity of METTL3. While different molecules displayed moderate inhibition of the human methyltransferase in vitro, multiple novel, potent and selective inhibitors of enterovirus 71 were identified. |
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College: |
Faculty of Science and Engineering |
Funders: |
This research was partly funded by the Sˆer Cymru II programme,
part-funded by Cardiff and Swansea Universities and the European
Regional Development Fund through the Welsh Government. |
Start Page: |
114942 |