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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/75155
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dc.contributor.authorMa, M.-
dc.contributor.authorKaras, J.-
dc.contributor.authorWhite, J.-
dc.contributor.authorScanlon, D.-
dc.contributor.authorDonnelly, P.-
dc.date.issued2009-
dc.identifier.citationChemical Communications, 2009; 14(22):3237-3239-
dc.identifier.issn1359-7345-
dc.identifier.issn1364-548X-
dc.identifier.urihttp://hdl.handle.net/2440/75155-
dc.description.abstractA new sarcophagine cage amine ligand with a pendent carboxylate functional group has been synthesised; the ligand has been conjugated to tumour targeting peptides ([Tyr3]- octreotate and [Lys3]-bombesin) and the conjugates radiolabelled with copper-64.-
dc.description.statementofresponsibilityMichelle T. Ma, John A. Karas, Jonathan M. White, Denis Scanlon and Paul S. Donnelly-
dc.language.isoen-
dc.publisherRoyal Soc Chemistry-
dc.rights© The Royal Society of Chemistry 2009-
dc.source.urihttp://dx.doi.org/10.1039/b903426a-
dc.subjectAnimals-
dc.subjectHumans-
dc.subjectCopper-
dc.subjectAmines-
dc.subjectCarboxylic Acids-
dc.subjectPeptides-
dc.subjectChelating Agents-
dc.subjectCross-Linking Reagents-
dc.subjectRadiopharmaceuticals-
dc.subjectLigands-
dc.titleA new bifunctional chelator for copper radiopharmaceuticals: a cage amine ligand with a carboxylate functional group for conjugation to peptides-
dc.typeJournal article-
dc.identifier.doi10.1039/B903426A-
pubs.publication-statusPublished-
Appears in Collections:Aurora harvest
Medical Sciences publications

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