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dc.contributor.authorFares, Mohamed
dc.contributor.authorWu, Xin
dc.contributor.authorRamesh, Deepthi
dc.contributor.authorLewis, William
dc.contributor.authorKeller, Paul A.
dc.contributor.authorHowe, Ethan N.W.
dc.contributor.authorPérez-Tomás, Ricardo
dc.contributor.authorGale, Philip A.
dc.date.accessioned2020-10-26
dc.date.available2020-10-26
dc.date.issued2020-01-01en
dc.identifier.urihttps://hdl.handle.net/2123/23683
dc.description.abstractAnion transporters have shown potential application as anti-cancer agents that function by disrupting homeostasis and triggering cell death. In this research article we report switchable anion transport by gold complexes of anion transporters that are ‘switched on’ in situ in the presence of the reducing agent GSH by decomplexation of gold. GSH is found in higher concentrations in tumours than in healthy tissue and hence this approach offers a strategy to target these systems to tumours.en
dc.language.isoenen
dc.publisherWiley-VCH GmbHen
dc.relation.ispartofAngewandte Chemie International Editionen
dc.rightsCopyright All Rights Reserveden
dc.subjectanion transport · gold complexes · molecular switch · reduction kinetics · supramolecular chemistryen
dc.titleStimuli-responsive cycloaurated ‘OFF-ON’ switchable anion transportersen
dc.typeArticleen
dc.subject.asrc0303 Macromolecular and Materials Chemistryen
dc.identifier.doi10.1002/anie.202006392
dc.relation.arcDP200100453
dc.rights.other"This is the peer reviewed version of the following articleM. Fares, X. Wu, D. Ramesh, W. Lewis, P. A. Keller, E. N. W. Howe, R. Pérez-Tomás, P. A. Gale, Angew. Chem. Int. Ed. 2020, 59, 17614,,which has been published in final form at https://doi.org/10.1002/anie.202006392.This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.en
usyd.facultySeS faculties schools::Faculty of Science::School of Chemistryen
usyd.citation.volume59en
usyd.citation.spage17614en
usyd.citation.epage17621en
workflow.metadata.onlyNoen


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