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dc.contributor.authorHataichanok Chuljermen_US
dc.contributor.authorYu Lin Chenen_US
dc.contributor.authorSomdet Srichairatanakoolen_US
dc.contributor.authorRobert C. Hideren_US
dc.contributor.authorAgostino Cilibrizzien_US
dc.date.accessioned2020-04-02T15:01:17Z-
dc.date.available2020-04-02T15:01:17Z-
dc.date.issued2019-01-01en_US
dc.identifier.issn14779234en_US
dc.identifier.issn14779226en_US
dc.identifier.other2-s2.0-85075692395en_US
dc.identifier.other10.1039/c9dt02731aen_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85075692395&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/67686-
dc.description.abstractThis journal is © The Royal Society of Chemistry. The iron(iii) affinity constants for schizokinen and its imide derivative are reported for the first time. Surprisingly, schizokinen possesses a higher affinity for iron(iii) than desferrioxamine B; log KFeIII (FeL), 36.2 and 30.6, respectively. This increase in value is associated with the substitution of one hydroxamate function by an α-hydroxycarboxylate grouping. By virtue of the similarity of siderophore-iron(iii) complexes and siderophore-gallium(iii) complexes, schizokinen (which is a Gram positive siderophore) has potential for 68Ga PET-based imaging.en_US
dc.subjectChemistryen_US
dc.titleSynthesis and iron coordination properties of schizokinen and its imide derivativeen_US
dc.typeJournalen_US
article.title.sourcetitleDalton Transactionsen_US
article.volume48en_US
article.stream.affiliationsKing's College Londonen_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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