Structure-based design, synthesis, and study of pyrazolo[1,5-a][1,3,5]triazine derivatives as potent inhibitors of protein kinase CK2
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Quinalizarin as a potent, selective and cell-permeable inhibitor of protein kinase CK2Structural Basis for Dual Nucleotide Selectivity of Aminoglycoside 2″-Phosphotransferase IVa Provides Insight on Determinants of Nucleotide Specificity of Aminoglycoside KinasesPotent and Selective Inhibitors of CK2 Kinase Identified through Structure-Guided HybridizationStructure and Property Based Design of Pyrazolo[1,5-a]pyrimidine Inhibitors of CK2 Kinase with Activity in VivoIdentification of a Potent Allosteric Inhibitor of Human Protein Kinase CK2 by Bacterial Surface Display Library Screening.Protein kinase CK2 inhibitors: a patent review.Casein kinases as potential therapeutic targets.Exploring the prominent performance of CX-4945 derivatives as protein kinase CK2 inhibitors by a combined computational study.Design and synthesis of a novel class of CK2 inhibitors: application of copper- and gold-catalysed cascade reactions for fused nitrogen heterocycles.Structure-Based Pharmacophore Modeling from Multicomplex: a Comprehensive Pharmacophore Generation of Protein Kinase CK2 and Virtual Screening Based on it for Novel Inhibitors.Exploring the Pivotal Role of the CK2 Hinge Region Sub-Pocket in Binding with Tricyclic Quinolone Analogues by Computational Analysis.Synthesis and Antiproliferative Activity of Novel Heterocyclic Indole-Trimethoxyphenyl Conjugates.Computational Macrocyclization: From de novo Macrocycle Generation to Binding Affinity Estimation.Diversity-oriented synthesis of pyrazolo[4,3-b]indoles by gold-catalysed three-component annulation: application to the development of a new class of CK2 inhibitors.Synthesis, Characterization, and Tautomerism of 1,3-Dimethyl Pyrimidine-2,4,6-Trione s-Triazinyl Hydrazine/Hydrazone DerivativesSynthesis, Crystal Structure and DFT Studies of 1,3-Dimethyl-5-propionylpyrimidine-2,4,6(1H,3H,5H)-trioneUltrasonic Irradiation: Synthesis, Characterization, and Preliminary Antimicrobial Activity of Novel Series of 4,6-Disubstituted-1,3,5-triazine Containing Hydrazone Derivatives
P2860
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P2860
Structure-based design, synthesis, and study of pyrazolo[1,5-a][1,3,5]triazine derivatives as potent inhibitors of protein kinase CK2
description
2007 nî lūn-bûn
@nan
2007 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Structure-based design, synthe ...... hibitors of protein kinase CK2
@ast
Structure-based design, synthe ...... hibitors of protein kinase CK2
@en
Structure-based design, synthe ...... hibitors of protein kinase CK2
@nl
type
label
Structure-based design, synthe ...... hibitors of protein kinase CK2
@ast
Structure-based design, synthe ...... hibitors of protein kinase CK2
@en
Structure-based design, synthe ...... hibitors of protein kinase CK2
@nl
prefLabel
Structure-based design, synthe ...... hibitors of protein kinase CK2
@ast
Structure-based design, synthe ...... hibitors of protein kinase CK2
@en
Structure-based design, synthe ...... hibitors of protein kinase CK2
@nl
P2093
P1476
Structure-based design, synthe ...... hibitors of protein kinase CK2
@en
P2093
April Averill
Carin Perretta
Kraig M Yager
Philip Erickson
Robert Almassy
Shaosong Chu
Stephen Margosiak
P304
P356
10.1016/J.BMCL.2007.05.041
P407
P577
2007-08-01T00:00:00Z