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Rapid identification of methylglyoxal trapping constituents from onion peels by pre-column incubation method

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dc.contributor.authorKim, Ji Hoon-
dc.contributor.authorKim, Myeong Il-
dc.contributor.authorSyed, Ahmed Shah-
dc.contributor.authorJung, Kiwon-
dc.contributor.authorKim, Chul Young-
dc.date.accessioned2021-06-22T15:23:21Z-
dc.date.available2021-06-22T15:23:21Z-
dc.date.created2021-01-22-
dc.date.issued2017-12-
dc.identifier.issn1226-3907-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/11621-
dc.description.abstractThe methylglyoxal (MGO) trapping constituents from onion (Allium cepa L.) peels were investigated using pre-column incubation of MGO and crude extract followed by HPLC analysis. The peak areas of MGO trapping compounds decreased, and their chemical structures were identified by HPLC-ESI/MS. Among major constituents in outer scale of onion, 2-(3,4-dihydroxybenzoyl)-2,4,6-trihydroxy-3(2H)-benzofuranone (2) was more effective MGO scavenger than quercetin (6) and its 4′-glucoside, spiraeoside (3). After 1 h incubation, compound 2 trapped over 90% MGO at a concentration of 0.5 mM under physiological conditions, but compounds 3 and 6 scavenged 45%, 16% MGO, respectively. HPLC-ESI/MS showed that compound 2 trapped two molecules of MGO to form a di-MGO adduct and compounds 3 and 6 captured one molecule of MGO to form mono-MGO adducts, and the positions 6 and 8 of the A ring of flavonoids were major active sites for trapping MGO. © 2017, Korean Society of Pharmacognosy. All rights reserved.-
dc.language영어-
dc.language.isoen-
dc.publisherKorean Society of Pharmacognosy-
dc.titleRapid identification of methylglyoxal trapping constituents from onion peels by pre-column incubation method-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Chul Young-
dc.identifier.doi10.20307/nps.2017.23.4.247-
dc.identifier.scopusid2-s2.0-85041037260-
dc.identifier.bibliographicCitationNatural Product Sciences, v.23, no.4, pp.247 - 252-
dc.relation.isPartOfNatural Product Sciences-
dc.citation.titleNatural Product Sciences-
dc.citation.volume23-
dc.citation.number4-
dc.citation.startPage247-
dc.citation.endPage252-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.identifier.kciidART002294534-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.subject.keywordPlus2 (3,4 dihydroxybenzoyl) 2,4,6 trihydroxy 3 benzofuranone-
dc.subject.keywordPlus3 benzofuranone derivative-
dc.subject.keywordPlusflavonoid-
dc.subject.keywordPlusmethylglyoxal-
dc.subject.keywordPlusquercetin-
dc.subject.keywordPlusspiraeoside-
dc.subject.keywordPlusunclassified drug-
dc.subject.keywordPlusArticle-
dc.subject.keywordPluschemical structure-
dc.subject.keywordPlusconcentration response-
dc.subject.keywordPluselectrospray mass spectrometry-
dc.subject.keywordPlushigh performance liquid chromatography-
dc.subject.keywordPlusincubation time-
dc.subject.keywordPlusnonhuman-
dc.subject.keywordPlusonion-
dc.subject.keywordPlusreaction time-
dc.subject.keywordAuthorAllium cepa L-
dc.subject.keywordAuthorFlavonoids-
dc.subject.keywordAuthorMethylglyoxal trapping-
dc.subject.keywordAuthorPre-column incubation-
dc.identifier.urlhttps://synapse.koreamed.org/articles/1060675-
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