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dc.contributor.author윤주영*
dc.date.accessioned2016-08-29T12:08:52Z-
dc.date.available2016-08-29T12:08:52Z-
dc.date.issued2016*
dc.identifier.issn0003-2700*
dc.identifier.otherOAK-18706*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/231595-
dc.description.abstractIn this study, we developed a turn-on mitochondria-targeting hydrogen sulfide, "probe 1", based on the selective thiolysis of 7-nitro-1,2,3-benzoxadiazole amine moiety attached to the piperazine-based naphthalimide scaffold. Probe 1 exhibited excellent properties with 68-fold fluorescence enhancement, a low detection limit (2.46 μM), a low cytotoxicity, and a good selectivity toward hydrogen sulfide. The success of intracellular imaging indicated that probe 1 could be used in further applications for the investigation of biological functions and pathological roles of H2S in living systems. © 2016 American Chemical Society.*
dc.languageEnglish*
dc.publisherAmerican Chemical Society*
dc.titleMitochondria-Targeted Reaction-Based Fluorescent Probe for Hydrogen Sulfide*
dc.typeArticle*
dc.relation.issue10*
dc.relation.volume88*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage5476*
dc.relation.lastpage5481*
dc.relation.journaltitleAnalytical Chemistry*
dc.identifier.doi10.1021/acs.analchem.6b00956*
dc.identifier.wosidWOS:000376223500062*
dc.identifier.scopusid2-s2.0-84969626849*
dc.author.googlePak Y.L.*
dc.author.googleLi J.*
dc.author.googleKo K.C.*
dc.author.googleKim G.*
dc.author.googleLee J.Y.*
dc.author.googleYoon J.*
dc.contributor.scopusid윤주영(7403587371)*
dc.date.modifydate20240118162450*
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자연과학대학 > 화학·나노과학전공 > Journal papers
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