Cinnamaldehydes inhibit cyclin dependent kinase 4/cyclin D1

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dc.contributor.authorHa Won Jeong-
dc.contributor.authorMi Ran Kim-
dc.contributor.authorKwang Hee Son-
dc.contributor.authorMi Young Han-
dc.contributor.authorJi Hong Ha-
dc.contributor.authorMatthieu Garnier-
dc.contributor.authorLaurent Meijer-
dc.contributor.authorByoung-Mog Kwon-
dc.date.accessioned2017-04-19T08:57:04Z-
dc.date.available2017-04-19T08:57:04Z-
dc.date.issued2000-
dc.identifier.issn0960-894X-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/5097-
dc.description.abstractA series of cinnamaldehydes was synthesized for the study of inhibitory activity against cyclin dependent kinases (CDKs). A couple of compounds selectively inhibited cyclin D1-CDK4 with an IC50 value of 7-18 μM.-
dc.publisherElsevier-
dc.titleCinnamaldehydes inhibit cyclin dependent kinase 4/cyclin D1-
dc.title.alternativeCinnamaldehydes inhibit cyclin dependent kinase 4/cyclin D1-
dc.typeArticle-
dc.citation.titleBioorganic & Medicinal Chemistry Letters-
dc.citation.number16-
dc.citation.endPage1822-
dc.citation.startPage1819-
dc.citation.volume10-
dc.contributor.affiliatedAuthorHa Won Jeong-
dc.contributor.affiliatedAuthorKwang Hee Son-
dc.contributor.affiliatedAuthorMi Young Han-
dc.contributor.affiliatedAuthorByoung-Mog Kwon-
dc.contributor.alternativeName정하원-
dc.contributor.alternativeName김미란-
dc.contributor.alternativeName손광희-
dc.contributor.alternativeName한미영-
dc.contributor.alternativeName하지홍-
dc.contributor.alternativeNameGarnier-
dc.contributor.alternativeNameMeijer-
dc.contributor.alternativeName권병목-
dc.identifier.bibliographicCitationBioorganic & Medicinal Chemistry Letters, vol. 10, no. 16, pp. 1819-1822-
dc.identifier.doi10.1016/S0960-894X(00)00357-7-
dc.description.journalClassY-
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Division of A.I. & Biomedical Research > Microbiome Convergence Research Center > 1. Journal Articles
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