Please use this identifier to cite or link to this item: https://apo.ansto.gov.au/dspace/handle/10238/9236
Title: Synthesis of 1,4-triazole linked zanamivir dimers as highly potent inhibitors of influenza A and B
Authors: Fraser, BH
Hamilton, S
Krause-Heuer, AM
Wright, PJ
Greguric, I
Tucker, SP
Draffan, AG
Fokin, VV
Sharpless, KB
Keywords: Synthesis
Triazoles
Dimers
Influenza
Enzyme inhibitors
Viruses
Lungs
Tissues
Issue Date: 29-Nov-2012
Publisher: The Royal Society of Chemistry
Citation: Fraser, B. H., Hamilton, S., Krause-Heuer, A. M., Wright, P. J., Greguric, I., Tucker, S. P., Draffan, A. G., Fokin, V. V., & Sharpless, K. B. (2013). Synthesis of 1, 4-triazole linked zanamivir dimers as highly potent inhibitors of influenza A and B. RSC Mediconal Chemistry, 4(2), 383-386. doi.10.1039/C2MD20300F
Abstract: The copper catalyzed azide alkyne cycloaddition (CuAAC) reaction – the quintessential ‘click’ reaction – was used to synthesise dimers of the neuraminidase inhibitor zanamivir in high yields. The effect upon anti-viral activity of varying the linker length and the number of triazole units was explored. All dimers were tested for anti-viral activity against influenza A/Sydney/5/97 and B/Harbin/7/94 in a cytopathic effect (CPE) assay. © Royal Society of Chemistry
Gov't Doc #: 8754
URI: https://doi.org/10.1039/C2MD20300F
http://apo.ansto.gov.au/dspace/handle/10238/9236
ISSN: 2632-8682
Appears in Collections:Journal Articles

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