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Cited 14 time in webofscience Cited 16 time in scopus
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Phenols displaying tyrosinase inhibition from Humulus lupulus

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dc.contributor.authorKim, Dae Wook-
dc.contributor.authorWoo, Hyun Sim-
dc.contributor.authorKim, Jeong Yoon-
dc.contributor.authorRyuk, Jin Ah-
dc.contributor.authorPark, Ki Hun-
dc.contributor.authorKo, Byoung Seob-
dc.date.accessioned2022-12-26T21:23:52Z-
dc.date.available2022-12-26T21:23:52Z-
dc.date.issued2016-
dc.identifier.issn1475-6366-
dc.identifier.issn1475-6374-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/16824-
dc.description.abstractTyrosinase is the rate-limiting enzyme for the production of melanin and other pigments via the oxidation of l-tyrosine. The methanol extract from Humulus lupulus showed potent inhibition against mushroom tyrosinase. The bioactivity-guided fractionation of this methanol extract resulted in the isolation of seven flavonoids (1-7), identified as xanthohumol (1), 4-O-methylxanthohumol (2), xanthohumol C (3), flavokawain C (4), xanthoumol B (5), 6-prenylnaringenin (6) and isoxanthohumol (7). All isolated flavonoids (1-7) effectively inhibited the monophenolase (IC(50)s=15.4-58.4 mu M) and diphenolase (IC(50)s=27.1-117.4 mu M) activities of tyrosinase. Kinetic studies using Lineweaver-Burk and Dixon-plots revealed that chalcones (1-5) were competitive inhibitors, whereas flavanones (6 and 7) exhibited both mixed and non-competitive inhibitory characteristics. In conclusion, this study is the first to demonstrate that the phenolic phytochemicals of H. lupulus display potent inhibitory activities against tyrosinase.-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisherTAYLOR & FRANCIS LTD-
dc.titlePhenols displaying tyrosinase inhibition from Humulus lupulus-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.3109/14756366.2015.1063621-
dc.identifier.scopusid2-s2.0-84976488792-
dc.identifier.wosid000379783700007-
dc.identifier.bibliographicCitationJOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, v.31, no.5, pp 742 - 747-
dc.citation.titleJOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY-
dc.citation.volume31-
dc.citation.number5-
dc.citation.startPage742-
dc.citation.endPage747-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.subject.keywordPlusXANTHOHUMOL-
dc.subject.keywordPlusHOPS-
dc.subject.keywordPlusPRENYLFLAVONOIDS-
dc.subject.keywordPlusMETABOLITES-
dc.subject.keywordPlusFLAVONOIDS-
dc.subject.keywordPlusPRODUCTS-
dc.subject.keywordPlusHEALTH-
dc.subject.keywordPlusBEER-
dc.subject.keywordAuthorCompetitive inhibition-
dc.subject.keywordAuthordiphenolase-
dc.subject.keywordAuthorHulumuls lupulus-
dc.subject.keywordAuthormonophenolase-
dc.subject.keywordAuthortyrosinase inhibitor-
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