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Cited 18 time in webofscience Cited 18 time in scopus
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dc.contributor.authorAhn, KH-
dc.contributor.authorLee, SJ-
dc.contributor.authorLee, CH-
dc.contributor.authorHong, CY-
dc.contributor.authorPark, TK-
dc.date.accessioned2016-03-31T13:41:53Z-
dc.date.available2016-03-31T13:41:53Z-
dc.date.created2009-08-07-
dc.date.issued1999-05-17-
dc.identifier.issn0960-894X-
dc.identifier.other1999-OAK-0000000748-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/20405-
dc.description.abstract3-Arylpyrrolidines are synthesized through the coupling of N-benzyl-3-(methanesulfonyloxy)pyrrolidine with diarylcuprates. Pharmacological evaluation of a series of N-substituted-3-arylpyrrolidines toward several neurotransmitter receptors indicated that some of them are good ligands for serotonin 1A receptor. Particularly, N-[(N-saccharino)butyl]pyrrolidines were found to be potent and selective ligands. A preliminary biological evaluation for several selected compounds indicated that they are potentially effective antianxiety and antidepressant agents. (C) 1999 Elsevier Science Ltd. All rights reserved.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.relation.isPartOfBIOORGANIC & MEDICINAL CHEMISTRY LETTERS-
dc.subjectENANTIOSELECTIVE SYNTHESIS-
dc.subjectANTIDEPRESSANT-
dc.subjectPYRROLIDINES-
dc.subjectABT-200-
dc.subjectAGENTS-
dc.titleN-substituted-3-arylpyrrolidines: Potent and selective ligands at serotonin 1A receptor-
dc.typeArticle-
dc.contributor.college분자소재융합계의 전자-광 거동연구센터-
dc.identifier.doi10.1016/S0960-894X(99)00201-2-
dc.author.googleAhn, KH-
dc.author.googleLee, SJ-
dc.author.googleLee, CH-
dc.author.googleHong, CY-
dc.author.googlePark, TK-
dc.relation.volume9-
dc.relation.issue10-
dc.relation.startpage1379-
dc.relation.lastpage1384-
dc.contributor.id10087916-
dc.relation.journalBIOORGANIC & MEDICINAL CHEMISTRY LETTERS-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationBIOORGANIC & MEDICINAL CHEMISTRY LETTERS, v.9, no.10, pp.1379 - 1384-
dc.identifier.wosid000080454300009-
dc.date.tcdate2019-01-01-
dc.citation.endPage1384-
dc.citation.number10-
dc.citation.startPage1379-
dc.citation.titleBIOORGANIC & MEDICINAL CHEMISTRY LETTERS-
dc.citation.volume9-
dc.contributor.affiliatedAuthorAhn, KH-
dc.identifier.scopusid2-s2.0-0033577775-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc17-
dc.type.docTypeArticle-
dc.subject.keywordPlusENANTIOSELECTIVE SYNTHESIS-
dc.subject.keywordPlusANTIDEPRESSANT-
dc.subject.keywordPlusPYRROLIDINES-
dc.subject.keywordPlusABT-200-
dc.subject.keywordPlusAGENTS-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalResearchAreaChemistry-

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안교한AHN, KYO HAN
Dept of Chemistry
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