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22 articles for thisTarget

The following articles (labelled with PubMed ID or TBD) are for your review
PMIDDataArticle TitleOrganization
15985434 18 Crystal structure of pyridoxal kinase in complex with roscovitine and derivatives.BDB Chinese Academy of Sciences
16616489 29 Suzuki-type Pd(0) coupling reactions in the synthesis of 2-arylpurines as Cdk inhibitors.BDB Institut Curie
10891109 19 Docking-based development of purine-like inhibitors of cyclin-dependent kinase-2.BDB Palacky University
10753466 15 Cyclin-dependent kinase inhibition by new C-2 alkynylated purine derivatives and molecular structure of a CDK2-inhibitor complex.BDB Institut Curie
10969976 13 Cinnamaldehydes inhibit cyclin dependent kinase 4/cyclin D1.BDB Korea Research Institute of Bioscience and Biotechnology
9871543 17 Synthesis of C2 alkynylated purines, a new family of potent inhibitors of cyclin-dependent kinases.BDB Institut Curie
11983514 17 Pyrazolo[3,4-b]quinoxalines. A new class of cyclin-dependent kinases inhibitors.BDB Universidad de Navarra
10465404 61 Synthesis and in vitro evaluation of novel 2,6,9-trisubstituted purines acting as cyclin-dependent kinase inhibitors.BDB Institut Curie
11960485 18 Structure-based design and synthesis of 2-benzylidene-benzofuran-3-ones as flavopiridol mimics.BDB Novartis Pharmaceuticals
14698171 21 1-Azakenpaullone is a selective inhibitor of glycogen synthase kinase-3 beta.BDB Technische Universitat Braunschweig
16250643 30 Pyrazolo[3,4-c]pyridazines as novel and selective inhibitors of cyclin-dependent kinases.BDB Universidad San Pablo CEU
15689157 28 Crystal structure of a human cyclin-dependent kinase 6 complex with a flavonol inhibitor, fisetin.BDB Lawrence Berkeley National Laboratory
15664865 37 Novel CDK inhibition profiles of structurally varied 1-aza-9-oxafluorenes.BDB Martin-Luther-University Halle-Wittenberg
14761195 114 Structural basis for the synthesis of indirubins as potent and selective inhibitors of glycogen synthase kinase-3 and cyclin-dependent kinases.BDB University of Athens
12519061 145 Aloisines, a new family of CDK/GSK-3 inhibitors. SAR study, crystal structure in complex with CDK2, enzyme selectivity, and cellular effects.BDB Faculte de Medecine et de Pharmacie
10998059 168 Paullones are potent inhibitors of glycogen synthase kinase-3beta and cyclin-dependent kinase 5/p25.BDB CNRS
14695817 67 Evaluation and comparison of 3D-QSAR CoMSIA models for CDK1, CDK5, and GSK-3 inhibition by paullones.BDB Universitat Hamburg
12941338 18 Structure-based design of 2-arylamino-4-cyclohexylmethyl-5-nitroso-6-aminopyrimidine inhibitors of cyclin-dependent kinases 1 and 2.BDB University of Newcastle
10956187 18 Identification of novel purine and pyrimidine cyclin-dependent kinase inhibitors with distinct molecular interactions and tumor cell growth inhibition profiles.BDB University of Newcastle
12482427 36 4-Alkoxy-2,6-diaminopyrimidine derivatives: inhibitors of cyclin dependent kinases 1 and 2.BDB University of Newcastle
15239650 90 N2-substituted O6-cyclohexylmethylguanine derivatives: potent inhibitors of cyclin-dependent kinases 1 and 2.BDB University of Newcastle
12139449 114 Probing the ATP ribose-binding domain of cyclin-dependent kinases 1 and 2 with O(6)-substituted guanine derivatives.BDB University of Newcastle