Agastaquinone, A new cytotoxic diterpenoid quinone from Agastache rugosa

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dc.contributor.authorHyeong Kyu Lee-
dc.contributor.authorSei Ryang Oh-
dc.contributor.authorJO Lee-
dc.contributor.authorJIN-WOONG KIM-
dc.contributor.authorCHONG-OCK LEE-
dc.date.accessioned2017-04-19T08:45:08Z-
dc.date.available2017-04-19T08:45:08Z-
dc.date.issued1995-
dc.identifier.issn0163-3864-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/3649-
dc.description.abstractA new diterpenoid quinone, agastaquinone [1], was isolated from the roots of Agastache rugosa. An oxime derivative [2] of agastaquinone was prepared with hydroxylamine hydrochloride. The structure of agastaquinone [1] was established as 7-hydroxy-12- methoxy-20-norabieta-1,5(10),6,812-pentaene-3,1,1,11-trione by spectroscopic techniques. Compounds 1 and 2 showed nonspecific cytotoic activities against several human cancer cell lines in vitro (A549, SK-OV-3, SK-MEL-2, XF198, and HCT15).-
dc.publisherAmer Chem Soc-
dc.titleAgastaquinone, A new cytotoxic diterpenoid quinone from Agastache rugosa-
dc.title.alternativeAgastaquinone, A new cytotoxic diterpenoid quinone from Agastache rugosa-
dc.typeArticle-
dc.citation.titleJournal of Natural Products-
dc.citation.number11-
dc.citation.endPage1721-
dc.citation.startPage1718-
dc.citation.volume58-
dc.contributor.affiliatedAuthorHyeong Kyu Lee-
dc.contributor.affiliatedAuthorSei Ryang Oh-
dc.contributor.affiliatedAuthorJO Lee-
dc.contributor.alternativeName이형규-
dc.contributor.alternativeName오세량-
dc.contributor.alternativeName김정일-
dc.contributor.alternativeName김진웅-
dc.contributor.alternativeName이정욱-
dc.identifier.bibliographicCitationJournal of Natural Products, vol. 58, no. 11, pp. 1718-1721-
dc.identifier.doi10.1021/np50125a011-
dc.description.journalClassY-
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Ochang Branch Institute > 1. Journal Articles
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