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dc.contributor.author고수영-
dc.date.accessioned2016-08-27T02:08:35Z-
dc.date.available2016-08-27T02:08:35Z-
dc.date.issued2007-
dc.identifier.issn0253-2964-
dc.identifier.otherOAK-3893-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/216073-
dc.description.abstractThe 5-HT6 antagonists are mainly related to the treatment of cognitive dysfunction or impairment associated with Alzheimer's disease and schizophrenia. There have been lots of efforts to develop 5-HT6 antagonists. As in our efforts, arylsulfonylpiperazine derivatives 1-3 were designed, synthesized and biologically evaluated against the human recombinant 5-HT6 serotonin receptor. Total 36 compounds were synthesized and the most active compound among the synthesized compounds is compound 2h with an IC50 value of 1.5 mu M. The compound 2h is novel as 5-HT6 receptor ligand and could act as lead for the novel 5-HT6 receptor ligands.-
dc.languageEnglish-
dc.publisherKOREAN CHEMICAL SOC-
dc.subjectserotonin-
dc.subject5-HT6 receptor-
dc.subjectantagonists-
dc.titleSynthesis and biological evaluation of arylsulfonylpiperazine derivatives as 5-HT6 receptor ligands-
dc.typeArticle-
dc.relation.issue2-
dc.relation.volume28-
dc.relation.indexSCI-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.indexKCI-
dc.relation.startpage285-
dc.relation.lastpage291-
dc.relation.journaltitleBULLETIN OF THE KOREAN CHEMICAL SOCIETY-
dc.identifier.wosidWOS:000245197800025-
dc.identifier.scopusid2-s2.0-33847243659-
dc.author.googleJeon, Sun Ah-
dc.author.googleChoo, Hyunah-
dc.author.googlePark, Woo-Kyu-
dc.author.googleRhim, Hyewhon-
dc.author.googleKo, Soo Y.-
dc.author.googleCho, Yong Seo-
dc.author.googleKoh, Hun Yeong-
dc.author.googlePae, Ae Nim-
dc.contributor.scopusid고수영(7403325351)-
dc.date.modifydate20230208103927-
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자연과학대학 > 화학·나노과학전공 > Journal papers
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