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dc.contributor.authorPae, AN-
dc.contributor.authorKim, SY-
dc.contributor.authorKim, HY-
dc.contributor.authorJoo, HJ-
dc.contributor.authorCho, YS-
dc.contributor.authorChoi, KI-
dc.contributor.authorChoi, JH-
dc.contributor.authorKoh, HY-
dc.date.accessioned2024-01-21T15:03:47Z-
dc.date.available2024-01-21T15:03:47Z-
dc.date.created2021-09-04-
dc.date.issued1999-09-20-
dc.identifier.issn0960-894X-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/141906-
dc.description.abstractThree-dimensional QSAR studies for two series of new oxazolidinone antibacterial agents were conducted using the comparative molecular field analysis (CoMFA). In vitro activities (MICs) of the compounds against methicillin-resistant Staphylococcus aureus 88 (MRSA 88) exhibited a strong correlation with their steric, electrostatic factors and lipophilicities. (C) 1999 Elsevier Science Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.title3D QSAR studies on new oxazolidinone antibacterial agents by comparative molecular field analysis-
dc.typeArticle-
dc.identifier.doi10.1016/S0960-894X(99)00474-6-
dc.description.journalClass1-
dc.identifier.bibliographicCitationBIOORGANIC & MEDICINAL CHEMISTRY LETTERS, v.9, no.18, pp.2685 - 2690-
dc.citation.titleBIOORGANIC & MEDICINAL CHEMISTRY LETTERS-
dc.citation.volume9-
dc.citation.number18-
dc.citation.startPage2685-
dc.citation.endPage2690-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000082759500011-
dc.identifier.scopusid2-s2.0-0033588856-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordAuthorQSAR-
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