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De Novo Design and Their Antimicrobial Activity of Stapled Amphipathic Helices of Heptapeptides

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dc.contributor.authorDinh, Thuy T. T.-
dc.contributor.authorKim, Do-Hee-
dc.contributor.authorLee, Song-Jin-
dc.contributor.authorKim, Young-Woo-
dc.date.accessioned2024-08-08T01:31:17Z-
dc.date.available2024-08-08T01:31:17Z-
dc.date.issued2014-12-20-
dc.identifier.issn0253-2964-
dc.identifier.issn1229-5949-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/15271-
dc.description.abstractIn this study we designed and synthesized several heptapeptides that are enforced to form an amphipathic helix using all-hydrocarbon stapling system and evaluated their antimicrobial and hemolytic activities. The antimicrobial activity showed clear structure-activity relationships, confirming the importance of helicity and amphipathicity. Some stapled heptapeptides displayed a moderate antimicrobial activity along with a low hemolytic activity. To our best knowledge, although not highly potent, these stapled peptides represent the shortest helical amphipathic antimicrobial peptides reported to date. The preliminary data obtained in this work would serve as a good starting point for further developing short analogs of amphipathic helical antimicrobial peptides.-
dc.format.extent5-
dc.language영어-
dc.language.isoENG-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.titleDe Novo Design and Their Antimicrobial Activity of Stapled Amphipathic Helices of Heptapeptides-
dc.typeArticle-
dc.publisher.location독일-
dc.identifier.doi10.5012/bkcs.2014.35.12.3632-
dc.identifier.scopusid2-s2.0-84920076603-
dc.identifier.wosid000346113000039-
dc.identifier.bibliographicCitationBULLETIN OF THE KOREAN CHEMICAL SOCIETY, v.35, no.12, pp 3632 - 3636-
dc.citation.titleBULLETIN OF THE KOREAN CHEMICAL SOCIETY-
dc.citation.volume35-
dc.citation.number12-
dc.citation.startPage3632-
dc.citation.endPage3636-
dc.type.docTypeArticle-
dc.identifier.kciidART001932328-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusCLOSING OLEFIN METATHESIS-
dc.subject.keywordPlusBIOLOGICAL-ACTIVITY-
dc.subject.keywordPlusPEPTIDES-
dc.subject.keywordPlusANTIBIOTICS-
dc.subject.keywordAuthorAntimicrobial peptides-
dc.subject.keywordAuthoralpha-Helix-
dc.subject.keywordAuthorStapled peptides-
dc.subject.keywordAuthorProtease resistance-
dc.subject.keywordAuthorPeptide drugs-
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