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dc.contributor.authorMarchal, Estelle
dc.contributor.authorSmithen, Deborah A.
dc.contributor.authorUddin, Md. Imam
dc.contributor.authorRobertson, Andrew W.
dc.contributor.authorJakeman, David L.
dc.contributor.authorVanessa, Mollard
dc.contributor.authorGoodman, Christopher D.
dc.contributor.authorMacDougall, Kristopher S.
dc.contributor.authorMcFarland, Sherri A.
dc.contributor.authorMcFadden, Geoffrey I.
dc.contributor.authorThompson, Alison
dc.date.accessioned2018-11-01T17:10:30Z
dc.date.available2018-11-01T17:10:30Z
dc.date.issued2014
dc.identifier.citationMarchal, E., Smithen, D. A., Uddin, M. I., Robertson, A. W., Jakeman, D. L., Mollard, V., ... & Thompson, A. (2014). Synthesis and antimalarial activity of prodigiosenes. Organic & biomolecular chemistry, 12(24), 4132-4142. DOI:b10.1039/C3OB42548Gen_US
dc.identifier.urihttp://hdl.handle.net/10222/74925
dc.descriptionPost-printen_US
dc.description.abstractSeveral analogues of the natural compound prodigiosin with modified A- and C-rings were synthesised as were some of their tin, cobalt, boron and zinc complexes. The antimalarial activity of these prodigiosenes was evaluated in vitro using the 3D7 Plasmodium falciparum strain. The presence of a nitrogen atom in the A-ring is needed for antimalarial activity but the presence of an alkyl group at the β’-position of the C-ring seems detrimental. Dibutyl tin complexes exhibit IC50 values mostly in the nanomolar range with equal or improved activity compared to the free-base prodigiosene ligand, despite the fact that the general toxicity of such tin complexes is demonstrably lower than that of the free-bases.en_US
dc.publisherOrganic and Biomolecular Chemistryen_US
dc.titleSynthesis and Antimalarial Activity of Prodigiosenesen_US
dc.typeArticleen_US
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