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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/42803
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dc.contributor.authorAvery, T.-
dc.contributor.authorMacreadie, P.-
dc.contributor.authorGreatrex, B.-
dc.contributor.authorRobinson, A.-
dc.contributor.authorTaylor, D.-
dc.contributor.authorMacreadie, I.-
dc.date.issued2007-
dc.identifier.citationBioorganic and Medicinal Chemistry, 2007; 15(1):36-42-
dc.identifier.issn0968-0896-
dc.identifier.issn1464-3391-
dc.identifier.urihttp://hdl.handle.net/2440/42803-
dc.descriptionAvailable online 13 October 2006-
dc.description.abstractBroad antifungal structure–activity relationships governing epoxy-endoperoxides 2 and 3 and their parent endoperoxides 1 are reported. Their inhibitory activity against Candida albicans in conjunction with hemolytic activity and/or growth inhibition of cultured mammalian cells are reported. This information provided guidance for the further development of endoperoxide and epoxy-endoperoxides as topical antifungal agents.-
dc.description.statementofresponsibilityThomas D. Avery, Peter I. Macreadie, Ben W. Greatrex, Tony V. Robinson, Dennis K. Taylor, and Ian G. Macreadie-
dc.language.isoen-
dc.publisherPergamon-Elsevier Science Ltd-
dc.source.urihttp://dx.doi.org/10.1016/j.bmc.2006.10.021-
dc.subjectArtemisinin-
dc.titleDesign of endoperoxides with anti-Candida activity-
dc.typeJournal article-
dc.identifier.doi10.1016/j.bmc.2006.10.021-
pubs.publication-statusPublished-
dc.identifier.orcidAvery, T. [0000-0001-6882-5461]-
dc.identifier.orcidTaylor, D. [0000-0002-3302-4610] [0000-0002-4274-3983] [0000-0003-0633-7424]-
Appears in Collections:Aurora harvest 6
Chemistry publications

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