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In Vitro Activity of Diphenyleneiodonium toward Multidrug-Resistant Helicobacter pylori Strains

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dc.contributor.authorChung, Jun-Won-
dc.contributor.authorKim, Su Young-
dc.contributor.authorPark, Hee Jung-
dc.contributor.authorChung, Chang Su-
dc.contributor.authorLee, Hee Woo-
dc.contributor.authorLee, Sun Mi-
dc.contributor.authorKim, Inki-
dc.contributor.authorPak, Jhang Ho-
dc.contributor.authorLee, Gin Hyug-
dc.contributor.authorJeong, Jin-Yong-
dc.date.available2020-02-27T17:42:58Z-
dc.date.created2020-02-06-
dc.date.issued2017-09-
dc.identifier.issn1976-2283-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/5779-
dc.description.abstractBackground/Aims: The increased resistance of Helicobacter pylori to antibiotics has increased the need to develop new treatments for this bacterium. The aim of our study was to identify new drugs with anti-H. pylori activity. Methods: We screened a small molecule library the library of pharmacologically active compounds (LOPAC), which includes 1,280 pharmacologically active compounds to identify inhibitors of H. pylori growth. The minimal inhibitory concentrations (MICs) of antibiotics against multidrug-resistant H. pylori strains were determined using the agar dilution method. Results: We identified diphenyleneiodonium (DPI) as a novel anti H. pylori agent. The MIC values for DPI were <0.03 mu g/mL against all tested H. pylori strains. DPI also exhibited strong antibacterial activity against common gram-negative and gram-positive pathogenic bacteria. Conclusions: DPI may be a candidate anti-H. pylori drug for future development.-
dc.language영어-
dc.language.isoen-
dc.publisherEDITORIAL OFFICE GUT & LIVER-
dc.relation.isPartOfGUT AND LIVER-
dc.subjectGASTRIC EPITHELIAL-CELLS-
dc.subjectNADPH OXIDASE-
dc.subjectTRIPLE THERAPY-
dc.subjectERADICATION-
dc.subjectEXPRESSION-
dc.subjectINFECTION-
dc.subjectMETRONIDAZOLE-
dc.subjectAMOXICILLIN-
dc.subjectACTIVATION-
dc.subjectINHIBITORS-
dc.titleIn Vitro Activity of Diphenyleneiodonium toward Multidrug-Resistant Helicobacter pylori Strains-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000411046200011-
dc.identifier.doi10.5009/gnl16503-
dc.identifier.bibliographicCitationGUT AND LIVER, v.11, no.5, pp.648 - 654-
dc.identifier.kciidART002262822-
dc.identifier.scopusid2-s2.0-85032028848-
dc.citation.endPage654-
dc.citation.startPage648-
dc.citation.titleGUT AND LIVER-
dc.citation.volume11-
dc.citation.number5-
dc.contributor.affiliatedAuthorChung, Jun-Won-
dc.contributor.affiliatedAuthorKim, Su Young-
dc.contributor.affiliatedAuthorChung, Chang Su-
dc.contributor.affiliatedAuthorLee, Hee Woo-
dc.type.docTypeArticle-
dc.subject.keywordAuthorHelicobacter pylori-
dc.subject.keywordAuthorDiphenyleneiodonium-
dc.subject.keywordAuthorDrug resistance, multiple-
dc.subject.keywordAuthorAnti-bacterial agents-
dc.subject.keywordAuthorMinimal inhibitory concentration-
dc.subject.keywordPlusGASTRIC EPITHELIAL-CELLS-
dc.subject.keywordPlusNADPH OXIDASE-
dc.subject.keywordPlusTRIPLE THERAPY-
dc.subject.keywordPlusERADICATION-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusINFECTION-
dc.subject.keywordPlusMETRONIDAZOLE-
dc.subject.keywordPlusAMOXICILLIN-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusINHIBITORS-
dc.relation.journalResearchAreaGastroenterology & Hepatology-
dc.relation.journalWebOfScienceCategoryGastroenterology & Hepatology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
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