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Novel Approaches to Flavivirus Drug Discovery

Overview
Specialties Chemistry
Pharmacology
Date 2012 Mar 24
PMID 22439769
Citations 12
Authors
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Abstract

Introduction: The members of the family Flaviviridae, including West Nile virus, yellow fever virus and dengue virus, are important human pathogens that are expanding their impact around the globe. The four serotypes of dengue infect 50-100 million people each year, yet the only clinical treatment is supportive care to reduce symptoms. Drugs that employ novel inhibition mechanisms and targets are urgently needed to combat the growing incidence of dengue worldwide.

Areas Covered: The authors discuss recently discovered flavivirus inhibitors with a focus on antivirals targeting non-enzymatic proteins of the dengue virus lifecycle. Specifically, the authors discuss the flaviviruses, the need for novel inhibitors and the criteria for successful antiviral drug development. Current literature describing new advances in antiviral therapy at each stage of the flavivirus lifecycle (entry, endosomal escape, viral RNA processing and replication, assembly and immune evasion) are evaluated and summarized.

Expert Opinion: Overall, the prognosis of flavivirus antiviral drug development is positive: new effective compounds have been discovered and studied. However, repurposing existing compounds and a greater translation to the clinical setting are recommended in order to combat the growing threat of flaviviruses.

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References
1.
Issur M, Geiss B, Bougie I, Picard-Jean F, Despins S, Mayette J . The flavivirus NS5 protein is a true RNA guanylyltransferase that catalyzes a two-step reaction to form the RNA cap structure. RNA. 2009; 15(12):2340-50. PMC: 2779676. DOI: 10.1261/rna.1609709. View

2.
Wang Q, Patel S, Vangrevelinghe E, Xu H, Rao R, Jaber D . A small-molecule dengue virus entry inhibitor. Antimicrob Agents Chemother. 2009; 53(5):1823-31. PMC: 2681551. DOI: 10.1128/AAC.01148-08. View

3.
Kim H, Choi E, Delgado M, Granja J, Khasanov A, Kraehenbuehl K . Antibacterial agents based on the cyclic D,L-alpha-peptide architecture. Nature. 2001; 412(6845):452-5. DOI: 10.1038/35086601. View

4.
Seth Horne W, Wiethoff C, Cui C, Wilcoxen K, Amorin M, Ghadiri M . Antiviral cyclic D,L-alpha-peptides: targeting a general biochemical pathway in virus infections. Bioorg Med Chem. 2005; 13(17):5145-53. PMC: 1829313. DOI: 10.1016/j.bmc.2005.05.051. View

5.
Allison S, Stiasny K, Stadler K, Mandl C, Heinz F . Mapping of functional elements in the stem-anchor region of tick-borne encephalitis virus envelope protein E. J Virol. 1999; 73(7):5605-12. PMC: 112618. DOI: 10.1128/JVI.73.7.5605-5612.1999. View