A Rigid Bicyclic Platform for the Generation of Conformationally Locked Neuraminidase Inhibitors

dc.contributor.authorBrant, Michael G.
dc.contributor.authorWulff, Jeremy E.
dc.date.accessioned2020-06-21T13:30:52Z
dc.date.available2020-06-21T13:30:52Z
dc.date.copyright2012en_US
dc.date.issued2012
dc.description.abstractRapid mutation of the influenza virus through genetic mixing raises the prospect of new strains that are both highly transmissible and highly lethal, and which have the ability to evade both immunization strategies (through mutation of hemagglutinin) and current therapies (through mutation of neuraminidase). Inspired by a need for next-generation therapeutics, a synthetic strategy for a new class of rigid, bicyclic inhibitors of influenza neuraminidase is reported.en_US
dc.description.reviewstatusRevieweden_US
dc.description.scholarlevelFacultyen_US
dc.description.sponsorshipWe thank the Canadian Institutes of Health Research for funding and Dr. Martin Petric (BC Centre for Disease Control) for a sample of inactivated influenza virus. We also thank Dr. Allen Oliver (University of Notre Dame) for X-ray analysis, Dr. Martin Boulanger (UVic Biochemistry) for helpful discussions, and the UVic Genome BC Proteomics Centre for mass spectrometry support.en_US
dc.identifier.citationBrant, M. G. & Wulff, J. E. (2012). A rigid bicyclic platform for the generation of conformationally locked neuraminidase inhibitors. Organic Letters, 14(23), 5876-5879. https://doi.org/10.1021/ol3027939en_US
dc.identifier.urihttps://doi.org/10.1021/ol3027939
dc.identifier.urihttp://hdl.handle.net/1828/11868
dc.language.isoenen_US
dc.publisherOrganic Lettersen_US
dc.subject.departmentDepartment of Chemistry
dc.titleA Rigid Bicyclic Platform for the Generation of Conformationally Locked Neuraminidase Inhibitorsen_US
dc.typeArticleen_US

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