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Synthesis and antiviral evaluation of the 2′-C-methyl branched derivative of a nucleoside analog inhibitor of RNA viral infections, T-1106
Claire Pierra, Clément Counor, Richard Storer and Gilles Gosselin
Language English Country Czech Republic Media elektronický zdroj
- MeSH
- Antiviral Agents MeSH
- Biological Phenomena MeSH
- Hepatitis C MeSH
- Nucleosides MeSH
- Hepatitis Viruses MeSH
An example of a 2′-C-methyl branched nucleoside analogue bearing 3,4-dihydro-3-oxopyrazine-2-carboxamide as the base, namely 4-(2-C-methyl-β-D-ribofuranosyl)-3-oxo-3,4-dihydropyrazine-2-carboxamide, is reported. This compound was synthesized following a Vorbrüggen's glycosylation procedure in a few steps. When evaluated in cell culture experiments against a broad range of viruses, this compound did not exhibit any significant antiviral effect or cytotoxicity.
Current Address Summit Corporation plc 91 Milton Park Abingdon Oxfordshire OX14 4RY England
UMR 5247 CNRS UM1 UM2 Université Montpellier 2 CC 1704 34095 Montpellier Cedex 5 France
Synthesis and antiviral evaluation of the 2′-C-methyl branched derivative of a nucleoside analog inhibitor of RNA viral infections, T-1106 [elektronický zdroj] /
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