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dc.contributor.authorTadesse, S.-
dc.contributor.authorZhu, G.-
dc.contributor.authorMekonnen, L.-
dc.contributor.authorLenjisa, J.-
dc.contributor.authorYu, M.-
dc.contributor.authorBrown, M.-
dc.contributor.authorWang, S.-
dc.identifier.citationFuture Medicinal Chemistry, 2017; 9(13):1495-1506-
dc.description.abstractInhibitors of CDK4/6 have emerged as a powerful class of therapeutics for treatment of several malignancies. We herein describe the identification of a new series of molecules that demonstrated excellent selectivity for CDK4/6 over CDKs1, 7 and 9.Medicinal chemistry optimization led to the discovery of 58 and 69 that inhibited CDK4 and CDK4/6, respectively, with high potency and selectivity, and 58 and 69 exhibited potent antiproliferative activities in a panel of human cancer cell lines including leukemia, and cancers of the breast, colon, ovary, pancreas and prostate.Compounds 58 and 69 caused remarkable growth inhibition of melanoma cells, particularly the cells harboring multiple BRAF and NRAS mutations, via a CDK4/6-targeted mechanism of action. [Formula: see text].-
dc.description.statementofresponsibilitySolomon Tadesse, Ge Zhu, Laychiluh B Mekonnen, Jimma L Lenjisa, Mingfeng Yu, Michael P Brown, Shudong Wang-
dc.publisherFuture Science-
dc.rights© 2017 Future Science Ltd.-
dc.subjectCell Line, Tumor-
dc.subjectGTP Phosphohydrolases-
dc.subjectProto-Oncogene Proteins B-raf-
dc.subjectRetinoblastoma Protein-
dc.subjectMembrane Proteins-
dc.subjectProtein Kinase Inhibitors-
dc.subjectCell Proliferation-
dc.subjectBinding Sites-
dc.subjectProtein Structure, Tertiary-
dc.subjectProtein Binding-
dc.subjectStructure-Activity Relationship-
dc.subjectCyclin-Dependent Kinase 4-
dc.subjectCyclin-Dependent Kinase 6-
dc.subjectG1 Phase Cell Cycle Checkpoints-
dc.titleA novel series of N-(pyridin-2-yl)-4-(thiazol-5-yl)pyrimidin-2-amines as highly potent CDK4/6 inhibitors-
dc.typeJournal article-
dc.identifier.orcidBrown, M. [0000-0002-5796-1932] [0000-0002-6678-1407]-
Appears in Collections:Aurora harvest 4
Biochemistry publications

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