Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1925
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dc.contributor.authorMALWAL, SATISH R.en_US
dc.contributor.authorLabade, Ajayen_US
dc.contributor.authorAndhalkar, Abhijeet S.en_US
dc.contributor.authorSENGUPTA, KUNDANen_US
dc.contributor.authorCHAKRAPANI, HARINATHen_US
dc.date.accessioned2019-02-25T09:00:43Z
dc.date.available2019-02-25T09:00:43Z
dc.date.issued2014-08en_US
dc.identifier.citationChemical Communications, 50(78), 11533-11535.en_US
dc.identifier.issn1359-7345en_US
dc.identifier.issn1364-548Xen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1925-
dc.identifier.urihttps://doi.org/10.1039/C4CC05462Hen_US
dc.description.abstractWe describe here hitherto unexplored chemistry of the sulfinate ester functional group as being highly selective towards nucleophilic substitution by thiols at physiological pH. Using this cleavable trigger, an optical thiol probe that is suitable for thiol bioimaging has been developed.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectSulfinate esteren_US
dc.subjectThiol bioimagingen_US
dc.subjectCleavable triggeren_US
dc.subjectBiological nucleophiles including amino acidsen_US
dc.subject2014en_US
dc.titleA highly selective sulfinate ester probe for thiol bioimagingen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemical Communicationsen_US
dc.publication.originofpublisherForeignen_US
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