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dc.contributor.authorIşık, M.en_US
dc.contributor.authorGuliyev, R.en_US
dc.contributor.authorKolemen, S.en_US
dc.contributor.authorAltay, Y.en_US
dc.contributor.authorSenturk, B.en_US
dc.contributor.authorTekinay, T.en_US
dc.contributor.authorAkkaya, E. U.en_US
dc.date.accessioned2016-02-08T10:50:57Z
dc.date.available2016-02-08T10:50:57Z
dc.date.issued2014en_US
dc.identifier.issn1523-7060
dc.identifier.urihttp://hdl.handle.net/11693/25825
dc.description.abstractA selective probe for glutathione was designed and synthesized. The design incorporates spatial and photophysical constraints for the maximal emission signal. Thus, pHs, as well as the intracellular thiol concentrations, determine the emission signal intensity through a tight control of charge-transfer and PeT processes. The probe works satisfactorily inside the human breast adenocarcinoma cells, highlighting GSH distribution in the cytosol.en_US
dc.language.isoEnglishen_US
dc.source.titleOrganic Lettersen_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/ol501272zen_US
dc.titleDesigning an intracellular fluorescent probe for glutathione: two modulation sites for selective signal transductionen_US
dc.typeArticleen_US
dc.departmentDepartment of Chemistryen_US
dc.citation.spage3260en_US
dc.citation.epage3263en_US
dc.citation.volumeNumber16en_US
dc.citation.issueNumber12en_US
dc.identifier.doi10.1021/ol501272zen_US
dc.publisherAmerican Chemical Societyen_US
dc.identifier.eissn1523-7052


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