ANIMAL EXPERIMENT;
APOPTOSIS;
ARTICLE;
CELL VIABILITY;
CONTROLLED STUDY;
DRUG DISTRIBUTION;
DRUG POTENCY;
DRUG SELECTIVITY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
ENZYME INHIBITION;
IC 50;
NONHUMAN;
RAT;
SINGLE DRUG DOSE;
STRUCTURE ACTIVITY RELATION;
BENZIMIDAZOLES;
CASEIN KINASE II;
HUMANS;
PROTEIN KINASE INHIBITORS;
TRIAZOLES;
Cell cycle dependent regulation of protein kinase CK2 signaling to the nuclear matrix
doi: 10.1002/jcb.1043
Wang H, Yu S, Davis AT, Ahmed K (2003) Cell cycle dependent regulation of protein kinase CK2 signaling to the nuclear matrix. J Cell Biochem 88:812-822. doi: 10.1002/jcb.10438
Involvement of protein kinase CK2 in angiogenesis and retinal neovascularization
doi: 10.1167/iovs.04-0686
Ljubimov AV, Caballero S, Aoki AM, Pinna LA, Grant MB, Castellon R (2004) Involvement of protein kinase CK2 in angiogenesis and retinal neovascularization. Invest Ophthalmol Vis Sci 45:4583-4591. doi: 10.1167/ iovs.04-0686
Phosphoproteome analysis by mass spectrometry and its application to Saccharomyces cerevisiae
doi: 10.1038/nbt0302-301
Ficarro SB, McCleland ML, Stukenberg PT, Burke DJ, Ross MM, Shabanowitz J et al (2002) Phosphoproteome analysis by mass spectrometry and its application to Saccharomyces cerevisiae. Nat Biotechnol 20:301-305. doi: 10.1038/nbt0302-301
Protein kinase CK2: Signaling and tumorigenesis in the mammary gland
doi: 10.1023/A:1013108822847
Landesman-Bollag E, Song DH, Romieu-Mourez R, Sussman DJ, Cardiff RD, Sonenshein GE et al (2001) Protein kinase CK2: Signaling and tumorigenesis in the mammary gland. Mol Cell Biochem 227(1-2):153-165. doi: 10.1023/A:1013108822847
Selectivity of 4, 5, 6, 7-tetrabromobenzimidazole as an ATP-competitive potent inhibitor of protein kinase CK2 from various sources
doi: 10.1016/S0006-291X(03)00928-8
Zień P, Bretner M, Zasta̧piło K, Szyszka R, Shugar D (2003) Selectivity of 4, 5, 6, 7-tetrabromobenzimidazole as an ATP-competitive potent inhibitor of protein kinase CK2 from various sources. Biochem Biophys Res Commun 306:129-133. doi: 10.1016/ S0006-291X(03)00928-8
Optimization of protein kinase CK2 inhibitors derived from 4, 5, 6, 7-tetrabromobenzimidazole
doi: 10.1021/jm049854a
Pagano MA, Andrzejewska M, Ruzzene M, Sarno S, Cesaro L, Bain J et al (2004) Optimization of protein kinase CK2 inhibitors derived from 4, 5, 6, 7-tetrabromobenzimidazole. J Med Chem 47:6239-6247. doi: 10.1021/ jm049854a
Selectivity of 4,5,6,7-tetrabromobenzotriazole, an ATP site-directed inhibitor of protein kinase CK2 (casein kinase-2)
doi: 10.1016/S0014-5793(01)02404-8
Sarno S, Reddy H, Meggio F, Ruzzene M, Davies SP, Donella-Deana A et al (2001) Selectivity of 4,5,6,7-tetrabromobenzotriazole, an ATP site-directed inhibitor of protein kinase CK2 (casein kinase-2). FEBS Lett 496:44-48. doi: 10.1016/S0014-5793(01)02404-8
The ATP-binding site of protein kinase CK2 holds a positive electrostatic area and conserved water molecules
doi: 10.1002/cbic.200700307
Battistutta R, Mazzorana M, Cendron L, Bortolato A, Sarno S, Kazimierczuk Z et al (2007) The ATP-binding site of protein kinase CK2 holds a positive electrostatic area and conserved water molecules. ChemBioChem 8(15):1804-1809. doi: 10.1002/cbic.200700307
Tetrabromobenzotriazole (TBBt) and tetrabromobenzimidazole (TBBz) as selective inhibitors of protein kinase CK2: Evaluation of their effects on cells and different molecular forms of human CK2
Zień P, Duncan JS, Skierski J, Bretner M, Litchfield DW, Shugar D (2005) Tetrabromobenzotriazole (TBBt) and tetrabromobenzimidazole (TBBz) as selective inhibitors of protein kinase CK2: Evaluation of their effects on cells and different molecular forms of human CK2. Biochim Biophys Acta 1754:271-280
Isolation and characterization of recombinant human casein kinase II subunits alpha and beta from bacteria
doi: 10.1111/j.1432-1033.1991.tb15982.x
Grankowski N, Boldyreff B, Issinger OG (1991) Isolation and characterization of recombinant human casein kinase II subunits alpha and beta from bacteria. Eur J Biochem 198:25-30. doi: 10.1111/ j.1432-1033.1991.tb15982.x
Synthesis and biological activity of 1H-benzotriazole and 1H-benzimidazole analogues - Inhibitors of the NTpase/helicase of HCV and of some related Flaviviridae
Bretner M, Baier A, Kopańska K, Najda A, Schoof A, Reinholz M et al (2005) Synthesis and biological activity of 1H-benzotriazole and 1H-benzimidazole analogues - inhibitors of the NTpase/helicase of HCV and of some related Flaviviridae. Antivir Chem Chemother 16(5):315-326