23 articles for thisTarget

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The following articles (labelled with PubMed ID or TBD) are for your review

PMID	Data	Article Title	Organization
15985434	18	Crystal structure of pyridoxal kinase in complex with roscovitine and derivatives.	Chinese Academy of Sciences
16616489	29	Suzuki-type Pd(0) coupling reactions in the synthesis of 2-arylpurines as Cdk inhibitors.	Institut Curie
10891109	19	Docking-based development of purine-like inhibitors of cyclin-dependent kinase-2.	Palacky University
10753466	15	Cyclin-dependent kinase inhibition by new C-2 alkynylated purine derivatives and molecular structure of a CDK2-inhibitor complex.	Institut Curie
10969976	13	Cinnamaldehydes inhibit cyclin dependent kinase 4/cyclin D1.	Korea Research Institute of Bioscience and Biotechnology
9871543	17	Synthesis of C2 alkynylated purines, a new family of potent inhibitors of cyclin-dependent kinases.	Institut Curie
11983514	17	Pyrazolo[3,4-b]quinoxalines. A new class of cyclin-dependent kinases inhibitors.	Universidad De Navarra
10465404	61	Synthesis and in vitro evaluation of novel 2,6,9-trisubstituted purines acting as cyclin-dependent kinase inhibitors.	Institut Curie
11960485	18	Structure-based design and synthesis of 2-benzylidene-benzofuran-3-ones as flavopiridol mimics.	Novartis Pharmaceuticals
14698171	21	1-Azakenpaullone is a selective inhibitor of glycogen synthase kinase-3 beta.	Technische Universitat Braunschweig
16250643	32	Pyrazolo[3,4-c]pyridazines as novel and selective inhibitors of cyclin-dependent kinases.	Universidad San Pablo Ceu
15689157	28	Crystal structure of a human cyclin-dependent kinase 6 complex with a flavonol inhibitor, fisetin.	Lawrence Berkeley National Laboratory
15664865	37	Novel CDK inhibition profiles of structurally varied 1-aza-9-oxafluorenes.	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.	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.	Faculte De Medecine Et De Pharmacie
10998059	168	Paullones are potent inhibitors of glycogen synthase kinase-3beta and cyclin-dependent kinase 5/p25.	Cnrs
14695817	67	Evaluation and comparison of 3D-QSAR CoMSIA models for CDK1, CDK5, and GSK-3 inhibition by paullones.	Universitat Hamburg
12941338	18	Structure-based design of 2-arylamino-4-cyclohexylmethyl-5-nitroso-6-aminopyrimidine inhibitors of cyclin-dependent kinases 1 and 2.	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.	University of Newcastle
12482427	36	4-Alkoxy-2,6-diaminopyrimidine derivatives: inhibitors of cyclin dependent kinases 1 and 2.	University of Newcastle
15239650	90	N2-substituted O6-cyclohexylmethylguanine derivatives: potent inhibitors of cyclin-dependent kinases 1 and 2.	University of Newcastle
12139449	114	Probing the ATP ribose-binding domain of cyclin-dependent kinases 1 and 2 with O(6)-substituted guanine derivatives.	University of Newcastle