Structure-activity relationship of indoline-2-carboxylic acid N-(substituted)phenylamide derivatives

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dc.contributor.authorJ W Kwak-
dc.contributor.authorY Kim-
dc.contributor.authorH Park-
dc.contributor.authorJ Y Jang-
dc.contributor.authorK K Lee-
dc.contributor.authorW Yi-
dc.contributor.authorJ A Kwak-
dc.contributor.authorSong Kyu Park-
dc.contributor.authorHwan Mook Kim-
dc.contributor.authorKiho Lee-
dc.contributor.authorJong Soon Kang-
dc.contributor.authorS B Han-
dc.contributor.authorB Y Hwang-
dc.contributor.authorJ T Hong-
dc.contributor.authorJ K Jung-
dc.contributor.authorY Kim-
dc.contributor.authorJ Cho-
dc.contributor.authorH Lee-
dc.date.accessioned2017-04-19T09:19:09Z-
dc.date.available2017-04-19T09:19:09Z-
dc.date.issued2010-
dc.identifier.issn0960-894X-
dc.identifier.uri10.1016/j.bmcl.2010.06.004ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/9639-
dc.description.abstractChroman derivatives exhibited potent inhibitory activity of NF-κB. For SAR, the chroman scaffold was modified with an indoline moiety. A series of indoline-2-carboxylic acid N-(substituted)phenylamide derivatives were synthesized to explore their inhibitory activities of NF-κB and they were also evaluated for cytotoxicity against various cancer cell lines. Since intermediates with Boc showed outstanding results, various substituents in place of the Boc group were introduced additionally and these compounds were also evaluated for SAR.-
dc.publisherElsevier-
dc.titleStructure-activity relationship of indoline-2-carboxylic acid N-(substituted)phenylamide derivatives-
dc.title.alternativeStructure-activity relationship of indoline-2-carboxylic acid N-(substituted)phenylamide derivatives-
dc.typeArticle-
dc.citation.titleBioorganic & Medicinal Chemistry Letters-
dc.citation.number15-
dc.citation.endPage4623-
dc.citation.startPage4620-
dc.citation.volume20-
dc.contributor.affiliatedAuthorSong Kyu Park-
dc.contributor.affiliatedAuthorHwan Mook Kim-
dc.contributor.affiliatedAuthorKiho Lee-
dc.contributor.affiliatedAuthorJong Soon Kang-
dc.contributor.alternativeName곽재환-
dc.contributor.alternativeName김요섭-
dc.contributor.alternativeName박현정-
dc.contributor.alternativeName장재용-
dc.contributor.alternativeName이건국-
dc.contributor.alternativeName이원희-
dc.contributor.alternativeName곽정아-
dc.contributor.alternativeName박성규-
dc.contributor.alternativeName김환묵-
dc.contributor.alternativeName이기호-
dc.contributor.alternativeName강종순-
dc.contributor.alternativeName한상배-
dc.contributor.alternativeName황방연-
dc.contributor.alternativeName홍진태-
dc.contributor.alternativeName정재경-
dc.contributor.alternativeName김영수-
dc.contributor.alternativeName조정숙-
dc.contributor.alternativeName이희순-
dc.identifier.bibliographicCitationBioorganic & Medicinal Chemistry Letters, vol. 20, no. 15, pp. 4620-4623-
dc.identifier.doi10.1016/j.bmcl.2010.06.004-
dc.subject.keywordCytotoxic activity-
dc.subject.keywordIndoline-2-carboxamide-
dc.subject.keywordNF-κB inhibitors-
dc.subject.localcytotoxic activities-
dc.subject.localcytotoxic activity-
dc.subject.localCytotoxic activity-
dc.subject.localIndoline-2-carboxamide-
dc.subject.localNF-κB inhibitors-
dc.description.journalClassY-
Appears in Collections:
Ochang Branch Institute > Division of National Bio-Infrastructure > Laboratory Animal Resource & Research Center > 1. Journal Articles
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