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dc.contributor.author김철영-
dc.date.accessioned2019-08-05T07:00:03Z-
dc.date.available2019-08-05T07:00:03Z-
dc.date.issued2006-06-
dc.identifier.citationJOURNAL OF LIQUID CHROMATOGRAPHY & RELATED TECHNOLOGIES, v. 29, No. 6, Page. 869-875en_US
dc.identifier.issn1082-6076-
dc.identifier.issn1520-572X-
dc.identifier.urihttps://www.tandfonline.com/doi/full/10.1080/10826070500531391-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/108248-
dc.description.abstractMangiferin was separated from rhizomes of Anemarrhena asphodeloides extract using centrifugal partition chromatography (CPC) with a two-phase solvent system composed of ethyl acetate-isopropanol-water (3:2:5, v/v). Mangiferin (22.5 mg) was successfully isolated from methanolic extracts (957 mg) in only one step, and the purity of isolated compound was determined to be over 95% by HPLC analysis. The structure of mangiferin was identified by H-1, C-13 NMR and ESI-MS spectral data analysis.en_US
dc.description.sponsorshipThis work was supported by the Korea Research Foundation Grant (KRF‐2003‐015‐E00217).en_US
dc.language.isoen_USen_US
dc.publisherTAYLOR & FRANCIS INCen_US
dc.subjectcentrifugal partition chromatographyen_US
dc.subjectAnemarrhena asphodeloidesen_US
dc.subjectpreparative chromatographyen_US
dc.subjectmangiferinen_US
dc.subjectxanthone glycosideen_US
dc.titlePreparative isolation of mangiferin from Anemarrhena asphodeloides rhizomes by centrifugal partition chromatographyen_US
dc.typeArticleen_US
dc.relation.no6-
dc.relation.volume29-
dc.identifier.doi10.1080/10826070500531391-
dc.relation.page869-875-
dc.relation.journalJOURNAL OF LIQUID CHROMATOGRAPHY & RELATED TECHNOLOGIES-
dc.contributor.googleauthorKim, CY-
dc.contributor.googleauthorAhn, MJ-
dc.contributor.googleauthorKim, J-
dc.relation.code2007205340-
dc.sector.campusE-
dc.sector.daehakCOLLEGE OF PHARMACY[E]-
dc.sector.departmentDEPARTMENT OF PHARMACY-
dc.identifier.pidchulykim-
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COLLEGE OF PHARMACY[E](약학대학) > PHARMACY(약학과) > Articles
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