Nucleoside Inhibitors of Zika Virus
Language English Country United States Media print-electronic
Document type Journal Article
PubMed
27234417
DOI
10.1093/infdis/jiw226
PII: jiw226
Knihovny.cz E-resources
- Keywords
- Zika virus, antiviral, flavivirus, nucleoside analogue, therapy,
- MeSH
- Antiviral Agents chemistry isolation & purification pharmacology MeSH
- Chlorocebus aethiops MeSH
- Microbial Sensitivity Tests MeSH
- Nucleosides chemistry isolation & purification pharmacology MeSH
- Virus Replication drug effects MeSH
- Vero Cells MeSH
- Zika Virus drug effects physiology MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Antiviral Agents MeSH
- Nucleosides MeSH
There is growing evidence that Zika virus (ZIKV) can cause devastating infant brain defects and other neurological disorders in humans. However, no specific antiviral therapy is available at present. We tested a series of 2'-C- or 2'-O-methyl-substituted nucleosides, 2'-C-fluoro-2'-C-methyl-substituted nucleosides, 3'-O-methyl-substituted nucleosides, 3'-deoxynucleosides, derivatives with 4'-C-azido substitution, heterobase-modified nucleosides, and neplanocins for their ability to inhibit ZIKV replication in cell culture. Antiviral activity was identified when 2'-C-methylated nucleosides were tested, suggesting that these compounds might represent promising lead candidates for further development of specific antivirals against ZIKV.
Department of Virology Veterinary Research Institute Brno
Institute of Organic Chemistry and Biochemistry Czech Academy of Sciences Prague
National Institute of Health Dr Ricardo Jorge CEVDI INSA Águas de Moura Portugal
References provided by Crossref.org
Synthesis and Biological Profiling of Quinolino-Fused 7-Deazapurine Nucleosides
Nucleoside analogs as a rich source of antiviral agents active against arthropod-borne flaviviruses
Characterisation of Zika virus infection in primary human astrocytes
An Approach for Zika Virus Inhibition Using Homology Structure of the Envelope Protein