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dc.contributor.author권영주*
dc.date.accessioned2016-08-28T12:08:27Z-
dc.date.available2016-08-28T12:08:27Z-
dc.date.issued2011*
dc.identifier.issn0968-0896*
dc.identifier.otherOAK-7450*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/221516-
dc.description.abstractIn order to develop potent skin whitening agents, we have synthesized 17 hydroxyphenyl benzyl ether compounds and tested their melanin synthesis inhibitory activity, DPPH free radical scavenging activity and tyrosinase inhibitory activity. Compounds 32, 35 and 36 possessing 4-hydroxyphenyl benzyl ether structure showed excellent inhibitory capacity with almost 50-fold than arbutin used as a reference in the inhibition test of α-MSH stimulated melanin synthesis in B-16 cells. 4-Hydroxyphenyl benzyl ether compounds also showed good antioxidant activity in the DPPH free radical scavenging test. The tyrosinase function was effectively inhibited by 3,5-dihydroxyphenyl benzyl ether analogues, especially compounds 18, 22, and 24. © 2011 Elsevier Ltd. All rights reserved.*
dc.languageEnglish*
dc.titleSynthesis and anti-melanogenic activity of hydroxyphenyl benzyl ether analogues*
dc.typeArticle*
dc.relation.issue7*
dc.relation.volume19*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage2168*
dc.relation.lastpage2175*
dc.relation.journaltitleBioorganic and Medicinal Chemistry*
dc.identifier.doi10.1016/j.bmc.2011.02.044*
dc.identifier.wosidWOS:000288792400007*
dc.identifier.scopusid2-s2.0-79953197167*
dc.author.googleSapkota K.*
dc.author.googleRoh E.*
dc.author.googleLee E.*
dc.author.googleHa E.-M.*
dc.author.googleYang J.-H.*
dc.author.googleLee E.-S.*
dc.author.googleKwon Y.*
dc.author.googleKim Y.*
dc.author.googleNa Y.*
dc.contributor.scopusid권영주(12446435600)*
dc.date.modifydate20240422124907*
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약학대학 > 약학과 > Journal papers
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