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dc.contributor.author오세관*
dc.date.accessioned2017-02-15T08:02:20Z-
dc.date.available2017-02-15T08:02:20Z-
dc.date.issued2007*
dc.identifier.issn0968-0896*
dc.identifier.otherOAK-4030*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/234348-
dc.description.abstractA simple synthesis and biological properties of 1,3-diphenyl-2-propen-1-ones 18-22 and 25-26 are described. The key synthetic strategies involve Grignard reaction of aldehyde 2 and oxidation reaction of 8-12 in high yields. The prepared compounds 18-22 and 25-26 were evaluated for free-radical scavenging, suppression of LPS-induced NO generation, and anti-excitotoxicity in vitro. It was found that a couple of compounds, especially 21 and 26, were potent suppressors of NO generation and demonstrated anti-excitotoxicity with the concentration range 10-20 μM in vitro. © 2007 Elsevier Ltd. All rights reserved.*
dc.languageEnglish*
dc.titleSynthesis of 1,3-diphenyl-2-propen-1-one derivatives and evaluation of their biological activities*
dc.typeArticle*
dc.relation.issue12*
dc.relation.volume15*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage4098*
dc.relation.lastpage4105*
dc.relation.journaltitleBioorganic and Medicinal Chemistry*
dc.identifier.doi10.1016/j.bmc.2007.03.077*
dc.identifier.wosidWOS:000246870400015*
dc.identifier.scopusid2-s2.0-34247587038*
dc.author.googleJang S.*
dc.author.googleJung J.-C.*
dc.author.googleOh S.*
dc.contributor.scopusid오세관(7404103757)*
dc.date.modifydate20240118133340*
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의과대학 > 의학과 > Journal papers
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