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Development of carbapenem-based fluorogenic probes for the clinical screening of carbapenemase-producing bacteria

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dc.contributor.authorKim, Juhyeon-
dc.contributor.authorKim, Yihoon-
dc.contributor.authorAbdelazem, Ahmed Z.-
dc.contributor.authorKim, Hak Joong-
dc.contributor.authorChoo, Hyunah-
dc.contributor.authorKim, Hoon Seok-
dc.contributor.authorKim, Jung Ok-
dc.contributor.authorPark, Yeon-Joon-
dc.contributor.authorMin, Sun-Joon-
dc.date.accessioned2021-08-31T15:07:14Z-
dc.date.available2021-08-31T15:07:14Z-
dc.date.created2021-06-18-
dc.date.issued2020-01-
dc.identifier.issn0045-2068-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/58516-
dc.description.abstractThis report describes the synthesis of a library of fluorogenic carbapenemase substrates consisting of carbapenem derivatives, fluorescence dyes, and active cleavable linkers and their evaluation for specifically detecting carbapenemase-producing organisms (CPOs). We synthesized a series of compounds having three different types of linkers such as benzyl ether, carbamate, and amine using hydroxymethyl carbapenem 7a and hydroxyallyl carbapenem 7b as key intermediates. Probe 1b exhibited high stability and a prompt turn-on fluorescence signal upon hydrolysis by carbapenemases. In particular, the screening of clinical samples indicated that the probe 1b exhibited excellent selectivity to the CPOs over other beta-lactamases or non-carbapenemase producing bacteria, which may be of clinical use for the rapid and accurate detection of CPOs for timely diagnosis and treatment.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.subjectBETA-LACTAMASE-
dc.subjectPSEUDOMONAS-AERUGINOSA-
dc.subjectENTEROBACTERIACEAE-
dc.subjectRESISTANCE-
dc.subjectINHIBITORS-
dc.subjectPROPOSAL-
dc.subjectGENES-
dc.titleDevelopment of carbapenem-based fluorogenic probes for the clinical screening of carbapenemase-producing bacteria-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Hak Joong-
dc.identifier.doi10.1016/j.bioorg.2019.103405-
dc.identifier.scopusid2-s2.0-85076526923-
dc.identifier.wosid000505596300061-
dc.identifier.bibliographicCitationBIOORGANIC CHEMISTRY, v.94-
dc.relation.isPartOfBIOORGANIC CHEMISTRY-
dc.citation.titleBIOORGANIC CHEMISTRY-
dc.citation.volume94-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.subject.keywordPlusBETA-LACTAMASE-
dc.subject.keywordPlusPSEUDOMONAS-AERUGINOSA-
dc.subject.keywordPlusENTEROBACTERIACEAE-
dc.subject.keywordPlusRESISTANCE-
dc.subject.keywordPlusINHIBITORS-
dc.subject.keywordPlusPROPOSAL-
dc.subject.keywordPlusGENES-
dc.subject.keywordAuthorCarbapenems-
dc.subject.keywordAuthorCarbapenemase-producing bacteria-
dc.subject.keywordAuthorLinker-
dc.subject.keywordAuthorFluorescence-
dc.subject.keywordAuthorProbes-
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