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dc.contributor.author최선*
dc.date.accessioned2016-08-28T12:08:43Z-
dc.date.available2016-08-28T12:08:43Z-
dc.date.issued2012*
dc.identifier.issn0968-0896*
dc.identifier.otherOAK-8307*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/222225-
dc.description.abstractStructure-activity relationships for the A-region in a series of N-4-t-butylbenzyl 2-(4-methylsulfonylaminophenyl) propanamides as TRPV1 antagonists have been investigated. Among them, the 3-fluoro analogue 54 showed high binding affinity and potent antagonism for both rTRPV1 and hTRPV1 in CHO cells. Its stereospecific activity was demonstrated with marked selectivity for the (S)-configuration (54S versus 54R). A docking study of 54S with our hTRPV1 homology model highlighted crucial hydrogen bonds between the ligand and the receptor contributing to its potency. © 2011 Elsevier Ltd. All rights reserved.*
dc.languageEnglish*
dc.titleN-4-t-Butylbenzyl 2-(4-methylsulfonylaminophenyl) propanamide TRPV1 antagonists: Structure-activity relationships in the A-region*
dc.typeArticle*
dc.relation.issue1*
dc.relation.volume20*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage215*
dc.relation.lastpage224*
dc.relation.journaltitleBioorganic and Medicinal Chemistry*
dc.identifier.doi10.1016/j.bmc.2011.11.008*
dc.identifier.wosidWOS:000298633300022*
dc.identifier.scopusid2-s2.0-84855188641*
dc.author.googleKim Y.S.*
dc.author.googleKil M.-J.*
dc.author.googleKang S.-U.*
dc.author.googleRyu H.*
dc.author.googleKim M.S.*
dc.author.googleCho Y.*
dc.author.googleBhondwe R.S.*
dc.author.googleThorat S.A.*
dc.author.googleSun W.*
dc.author.googleLiu K.*
dc.author.googleLee J.H.*
dc.author.googleChoi S.*
dc.author.googlePearce L.V.*
dc.author.googlePavlyukovets V.A.*
dc.author.googleMorgan M.A.*
dc.author.googleTran R.*
dc.author.googleLazar J.*
dc.author.googleBlumberg P.M.*
dc.author.googleLee J.*
dc.contributor.scopusid최선(8659831000)*
dc.date.modifydate20240305081003*
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약학대학 > 약학과 > Journal papers
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