DSpace at KISTKIST Article2002

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dc.contributor.authorLee, JY-
dc.contributor.authorPark, JH-
dc.contributor.authorLee, SJ-
dc.contributor.authorPark, H-
dc.contributor.authorLee, YS-
dc.date.accessioned2024-01-21T10:36:56Z-
dc.date.available2024-01-21T10:36:56Z-
dc.date.created2021-09-01-
dc.date.issued2002-06-
dc.identifier.issn0365-6233-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/139506-
dc.description.abstractStyrylquinazoline derivatives were prepared by Perkin condensation and evaluated for inhibitory activity against HIV-1 integrase. Among them, compound 5 c containing a free catechol ring was the most potent (IC50 = 20.8 +/- 1.9 muM) and showed 6-fold more potency than the corresponding styrylquinoline compound (IC50 = 130.7+/-8.6 muM).-
dc.languageEnglish-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.titleStyrylquinazoline derivatives as HIV-1 integrase inhibitors-
dc.typeArticle-
dc.identifier.doi10.1002/1521-4184(200208)335:6<277::AID-ARDP277>3.0.CO;2-A-
dc.description.journalClass1-
dc.identifier.bibliographicCitationARCHIV DER PHARMAZIE, v.335, no.6, pp.277 - 282-
dc.citation.titleARCHIV DER PHARMAZIE-
dc.citation.volume335-
dc.citation.number6-
dc.citation.startPage277-
dc.citation.endPage282-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000177596300004-
dc.identifier.scopusid2-s2.0-0036614688-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusREPLICATION-
dc.subject.keywordAuthorstyrylquinazoline-
dc.subject.keywordAuthorPerkin condensation-
dc.subject.keywordAuthorAIDS-
dc.subject.keywordAuthorHIV-
dc.subject.keywordAuthorintegrase inhibitor-
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