Development of tripeptidyl farnesyltransferase inhibitors

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dc.contributor.authorLee, Hee Yoonko
dc.contributor.authorSohn, JHko
dc.contributor.authorKwon, BMko
dc.date.accessioned2013-03-03T22:08:18Z-
dc.date.available2013-03-03T22:08:18Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2002-06-
dc.identifier.citationBIOORGANIC MEDICINAL CHEMISTRY LETTERS, v.12, no.12, pp.1599 - 1602-
dc.identifier.issn0960-894X-
dc.identifier.urihttp://hdl.handle.net/10203/80657-
dc.description.abstractThe first example of tripeptide inhibitors of farnesyltransferase with sub-micromolar inhibition activity was developed based on the fact that CVFM is not a substrate for farnesyltransferase. (C) 2002 Elsevier Science Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectFARNESYL-PROTEIN TRANSFERASE-
dc.subjectASYMMETRIC-SYNTHESIS-
dc.subjectALPHA-AMINO-
dc.subjectARTEMINOLIDE-
dc.subjectANALOG-
dc.subjectDESIGN-
dc.titleDevelopment of tripeptidyl farnesyltransferase inhibitors-
dc.typeArticle-
dc.identifier.wosid000176178700013-
dc.identifier.scopusid2-s2.0-0037124186-
dc.type.rimsART-
dc.citation.volume12-
dc.citation.issue12-
dc.citation.beginningpage1599-
dc.citation.endingpage1602-
dc.citation.publicationnameBIOORGANIC MEDICINAL CHEMISTRY LETTERS-
dc.contributor.localauthorLee, Hee Yoon-
dc.contributor.nonIdAuthorSohn, JH-
dc.contributor.nonIdAuthorKwon, BM-
dc.type.journalArticleArticle-
dc.subject.keywordPlusFARNESYL-PROTEIN TRANSFERASE-
dc.subject.keywordPlusASYMMETRIC-SYNTHESIS-
dc.subject.keywordPlusALPHA-AMINO-
dc.subject.keywordPlusARTEMINOLIDE-
dc.subject.keywordPlusANALOG-
dc.subject.keywordPlusDESIGN-
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