ATP site-directed inhibitors of protein kinase CK2: an update
about
A subnanomolar fluorescent probe for protein kinase CK2 interaction studiesStructure and Property Based Design of Pyrazolo[1,5-a]pyrimidine Inhibitors of CK2 Kinase with Activity in VivoCell-permeable dual inhibitors of protein kinases CK2 and PIM-1: structural features and pharmacological potentialThe Halogen BondEffects of the CK2 inhibitors CX-4945 and CX-5011 on drug-resistant cellsThe Thr205 phosphorylation site within respiratory syncytial virus matrix (M) protein modulates M oligomerization and virus productionMechanism and efficacy of sub-50-nm tenfibgen nanocapsules for cancer cell-directed delivery of anti-CK2 RNAi to primary and metastatic squamous cell carcinoma.Isomeric mono-, di-, and tri-bromobenzo-1H-triazoles as inhibitors of human protein kinase CK2α.Protein kinase CK2 inhibition down modulates the NF-κB and STAT3 survival pathways, enhances the cellular proteotoxic stress and synergistically boosts the cytotoxic effect of bortezomib on multiple myeloma and mantle cell lymphoma cells.Synthesis and properties of a selective inhibitor of homeodomain-interacting protein kinase 2 (HIPK2).Protein Kinase CK2 Expression Predicts Relapse Survival in ERα Dependent Breast Cancer, and Modulates ERα Expression in Vitro.Kinase inhibitors as potential agents in the treatment of multiple myeloma.In Search of Small Molecule Inhibitors Targeting the Flexible CK2 Subunit Interface.Protein kinase CK2 inhibitors: a patent review.PML Degradation: Multiple Ways to Eliminate PML.Casein kinase: the triple meaning of a misnomer.The protein kinase 2 inhibitor CX-4945 regulates osteoclast and osteoblast differentiation in vitro.Different Persistence of the Cellular Effects Promoted by Protein Kinase CK2 Inhibitors CX-4945 and TDB.Benzimidazole inhibitors of protein kinase CK2 potently inhibit the activity of atypical protein kinase Rio1An overview of quinoline as a privileged scaffold in cancer drug discovery.Exploring the Pivotal Role of the CK2 Hinge Region Sub-Pocket in Binding with Tricyclic Quinolone Analogues by Computational Analysis.Synthesis, Biological Evaluation and Molecular Modeling of Substituted Indeno[1,2-b]indoles as Inhibitors of Human Protein Kinase CK2.Unexpected Binding Mode of a Potent Indeno[1,2-b]indole-Type Inhibitor of Protein Kinase CK2 Revealed by Complex Structures with the Catalytic Subunit CK2α and Its Paralog CK2α'.Insights into the Impact of Linker Flexibility and Fragment Ionization on the Design of CK2 Allosteric Inhibitors: Comparative Molecular Dynamics Simulation Studies.Looking Back, Looking Forward at Halogen Bonding in Drug Discovery.
P2860
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P2860
ATP site-directed inhibitors of protein kinase CK2: an update
description
2011 nî lūn-bûn
@nan
2011 թուականին հրատարակուած գիտական յօդուած
@hyw
2011 թվականին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
ATP site-directed inhibitors of protein kinase CK2: an update
@ast
ATP site-directed inhibitors of protein kinase CK2: an update
@en
ATP site-directed inhibitors of protein kinase CK2: an update
@nl
type
label
ATP site-directed inhibitors of protein kinase CK2: an update
@ast
ATP site-directed inhibitors of protein kinase CK2: an update
@en
ATP site-directed inhibitors of protein kinase CK2: an update
@nl
prefLabel
ATP site-directed inhibitors of protein kinase CK2: an update
@ast
ATP site-directed inhibitors of protein kinase CK2: an update
@en
ATP site-directed inhibitors of protein kinase CK2: an update
@nl
P2093
P1476
ATP site-directed inhibitors of protein kinase CK2: an update
@en
P2093
A Orzeszko
C Franchin
E Papinutto
R Battistutta
Z Kazimierczuk
P304
P356
10.2174/156802611795589638
P577
2011-01-01T00:00:00Z