Cytotoxicity of triterpenes isolated from Aceriphyllum rossii

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dc.contributor.authorI Lee-
dc.contributor.authorJ K Yoo-
dc.contributor.authorM Na-
dc.contributor.authorB S Min-
dc.contributor.authorJ Lee-
dc.contributor.authorBong Sik Yun-
dc.contributor.authorW Y Jin-
dc.contributor.authorH Kim-
dc.contributor.authorU Youn-
dc.contributor.authorQ C Chen-
dc.contributor.authorK S Song-
dc.contributor.authorY H Seong-
dc.contributor.authorK Bae-
dc.date.accessioned2017-04-19T09:08:26Z-
dc.date.available2017-04-19T09:08:26Z-
dc.date.issued2007-
dc.identifier.issn0009-2363-
dc.identifier.uri10.1248/cpb.55.1376ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/8152-
dc.description.abstractBioassay-guided fractionation of a MeOH extract of the whole plant of Aceriphyllum rossii (Saxifragaceae) led to the isolation of two new triterpenes, 3 α,23-isopropylidenedioxyolean-12-en-27-oic acid (1) and 23-hydroxy-3-oxoolean-12-en-27-oic acid (2), together with six known triterpenes, 3-oxoolean-12-en-27-oic acid (3), 3 α-hydroxyolean-12-en-27- oic acid (4), β-peltoboykinolic acid (5), aceriphyllic acid A (6), oleanolic acid (7), and gypsogenic acid (8). The structures of these compounds were elucidated on the basis of physicochemical and spectroscopic analyses. These compounds were evaluated for in vitro cytotoxicity against the K562 and HL-60 cell lines. Olean-12-en-27-oic acid derivatives (1-6) exhibited considerable cytotoxicity against K562 and HL-60 cell lines with IC50 values ranging from 12.2 to 28.7 μM and from 12.1 to 25.8 μM, respectively.-
dc.publisherPharmaceutical Soc Japan-
dc.titleCytotoxicity of triterpenes isolated from Aceriphyllum rossii-
dc.title.alternativeCytotoxicity of triterpenes isolated from Aceriphyllum rossii-
dc.typeArticle-
dc.citation.titleChemical & Pharmaceutical Bulletin-
dc.citation.number9-
dc.citation.endPage1378-
dc.citation.startPage1376-
dc.citation.volume55-
dc.contributor.affiliatedAuthorBong Sik Yun-
dc.contributor.alternativeName이익수-
dc.contributor.alternativeName유재국-
dc.contributor.alternativeName나민균-
dc.contributor.alternativeName민병선-
dc.contributor.alternativeName이종필-
dc.contributor.alternativeName윤봉식-
dc.contributor.alternativeNameJin-
dc.contributor.alternativeName김홍진-
dc.contributor.alternativeName윤의정-
dc.contributor.alternativeNameChen-
dc.contributor.alternativeName송경식-
dc.contributor.alternativeName성연희-
dc.contributor.alternativeName배기환-
dc.identifier.bibliographicCitationChemical & Pharmaceutical Bulletin, vol. 55, no. 9, pp. 1376-1378-
dc.identifier.doi10.1248/cpb.55.1376-
dc.subject.keywordAceriphyllum rossii-
dc.subject.keywordCytotoxicity-
dc.subject.keywordSaxifragaceae-
dc.subject.keywordTriterpene-
dc.subject.localAceriphyllum rossii-
dc.subject.localaceriphyllum rossii-
dc.subject.localCytotoxicity-
dc.subject.localcytotoxicity-
dc.subject.localsaxifragaceae-
dc.subject.localSaxifragaceae-
dc.subject.localtriterpene-
dc.subject.localTriterpene-
dc.description.journalClassY-
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