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dc.contributor.authorAriawan, A. Daryl
dc.contributor.authorWebb, James E.A.
dc.contributor.authorHowe, Ethan N.W.
dc.contributor.authorGale, Philip A.
dc.contributor.authorThordarson, Pall
dc.contributor.authorHunter, Luke
dc.date.accessioned2019-02-07
dc.date.available2019-02-07
dc.date.issued2017-02-01
dc.identifier.citationA. Daryl Ariawan, J. E. A. Webb, E. N. W. Howe, P. A. Gale, P. Thordarson and L. Hunter, Org. Biomol. Chem., 2017, 15, 2962 DOI: 10.1039/c7ob00316aen
dc.identifier.urihttp://hdl.handle.net/2123/19953
dc.description.abstractUnguisin A (1) is a marine-derived, GABA-containing cyclic heptapeptide. The biological function of this flexible macrocycle is obscure. Here we show that compound 1 lacks any detectable activity in antimicrobial growth inhibition assays, a result that runs contrary to a previous report. However, we find that 1 functions as a promiscuous host molecule in a variety of anion-binding interactions, with high affinity particularly for phosphate and pyrophosphate. We also show that a series of rigidified, backbone-fluorinated analogues of 1 displays altered affinity for chloride ions.en
dc.description.sponsorshipARCen
dc.language.isoenen
dc.publisherRoyal Society of Chemistryen
dc.relationARC DP170100118en
dc.rightsOtheren
dc.subjectsupramolecular chemistryen
dc.titleCyclic peptide unguisin A is an anion receptor with high affinity for phosphate and pyrophosphateen
dc.typeArticleen
dc.subject.asrc030302en
dc.identifier.doi10.1039/c7ob00316a
dc.type.pubtypePost-printen
dc.rights.otherReproduced from Organic & Biomolecular Chemistry with permission from the Royal Society of Chemistry.en
usyd.facultyFaculty of Science, School of Chemistry


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