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dc.contributor.author유경호-
dc.contributor.author조혜정-
dc.date.accessioned2024-01-20T21:06:05Z-
dc.date.available2024-01-20T21:06:05Z-
dc.date.created2021-09-06-
dc.date.issued2009-06-
dc.identifier.issn1225-9098-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/132419-
dc.description.abstractIn this work, a novel series of aminoisoquinolinylamide derivatives 1a-c and 2a-f were synthesized via several reaction steps, starting from 2-methyl-4-nitrobenzonitrile (3) and 1-chloro-5-nitroquinoline (8). And their antiproliferative activities were screened against A375 human melanoma cell line compared to Sorafenib as a reference compound. Among them, compound 1b and 1c exhibited meaningful inhibitory activities. These results demonstrated that aminoisoquinolinylamide scaffold possesses the possibility as the treatment for melanoma.-
dc.languageKorean-
dc.publisher한국응용과학기술학회-
dc.title새로운 Aminoisoquinolinylamide 유도체의 합성 및 흑색종 저해 효능-
dc.typeArticle-
dc.description.journalClass2-
dc.identifier.bibliographicCitation한국응용과학기술학회지, v.26, no.2, pp.161 - 170-
dc.citation.title한국응용과학기술학회지-
dc.citation.volume26-
dc.citation.number2-
dc.citation.startPage161-
dc.citation.endPage170-
dc.description.journalRegisteredClasskci-
dc.identifier.kciidART001356879-
dc.subject.keywordAuthoraminoisoquinolinylamides-
dc.subject.keywordAuthorsynthesis-
dc.subject.keywordAuthorantiproliferative activity-
dc.subject.keywordAuthormelanoma cell line-
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