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dc.contributor.author유혜현-
dc.date.accessioned2019-08-20T07:21:14Z-
dc.date.available2019-08-20T07:21:14Z-
dc.date.issued2006-11-
dc.identifier.citationBIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, v. 70, No. 11, Page. 2783-2785en_US
dc.identifier.issn0916-8451-
dc.identifier.issn1347-6947-
dc.identifier.urihttps://www.jstage.jst.go.jp/article/bbb/70/11/70_60290/_article/-char/ja/-
dc.identifier.urihttp://repository.hanyang.ac.kr/handle/20.500.11754/108817-
dc.description.abstractThe lignan glycoside, tracheloside, was isolated from seeds of Carthamus tinctorius (Compositae) as an anti-estrogenic principle against cultured Ishikawa cells by employing a bioassay-linked HPLC-ELSD method. Tracheloside significantly decreased the activity of alkaline phosphatase (AP), an estrogen-inducible marker enzyme, with an IC50 value of 0.31 mu g/ml, a level of inhibition comparable to that of tamoxifen (IC50 = 0.43 mu g/ml).en_US
dc.language.isoen_USen_US
dc.publisherJAPAN SOC BIOSCI BIOTECHN AGROCHEMen_US
dc.subjectCarthamus tinctoriusen_US
dc.subjecttrachelosideen_US
dc.subjectanti-estrogenic activityen_US
dc.subjectIshikawa cellen_US
dc.subjectbioassay-linked HPLC-ELSDen_US
dc.titleAn anti-estrogenic lignan glycoside, tracheloside, from seeds of Carthamus tinctoriusen_US
dc.typeArticleen_US
dc.relation.volume70-
dc.identifier.doi10.1271/bbb.60290-
dc.relation.page2783-2785-
dc.relation.journalBIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY-
dc.contributor.googleauthorYOO, Hye Hyun-
dc.contributor.googleauthorPARK, Jeong Hill-
dc.contributor.googleauthorKWON, Sung Won-
dc.relation.code2009201342-
dc.sector.campusE-
dc.sector.daehakCOLLEGE OF PHARMACY[E]-
dc.sector.departmentDEPARTMENT OF PHARMACY-
dc.identifier.pidyoohh-
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COLLEGE OF PHARMACY[E](약학대학) > PHARMACY(약학과) > Articles
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