Compounds > staurosporine
Page last updated: 2024-08-23

staurosporine and dichlororibofuranosylbenzimidazole

staurosporine has been researched along with dichlororibofuranosylbenzimidazole in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's4 (80.00)29.6817
2010's1 (20.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bain, J; Battistutta, R; de Moliner, E; Elliott, M; Fabbro, D; Furet, P; Meggio, F; Pagano, MA; Pinna, LA; Ruzzene, M; Sarno, S; Schoepfer, J; Zanotti, G1
Bullock, AN; Fedorov, O; Knapp, S; Marsden, B; Müller, S; Pogacic, V; Rellos, P; Schwaller, J; Sundström, M1
Baumli, S; Endicott, JA; Fischer, PM; Hole, AJ; Huang, S; Noble, ME; Pepper, C; Shao, H; Shi, S; Wang, S1
Hendzel, MJ; Lever, MA; Sun, X; Th'ng, JP1
Chakraborty, S; Haldar, D; Onorato, TM1

Other Studies

5 other study(ies) available for staurosporine and dichlororibofuranosylbenzimidazole

ArticleYear
Biochemical and three-dimensional-structural study of the specific inhibition of protein kinase CK2 by [5-oxo-5,6-dihydroindolo-(1,2-a)quinazolin-7-yl]acetic acid (IQA).
    The Biochemical journal, 2003, Sep-15, Volume: 374, Issue:Pt 3

    Topics: Acetates; Animals; Casein Kinase II; Cell Line; Crystallography, X-Ray; Enzyme Inhibitors; Humans; Jurkat Cells; Molecular Structure; Plant Proteins; Protein Serine-Threonine Kinases; Protein Structure, Quaternary; Quinazolines; Rats; Zea mays

2003
A systematic interaction map of validated kinase inhibitors with Ser/Thr kinases.
    Proceedings of the National Academy of Sciences of the United States of America, 2007, Dec-18, Volume: 104, Issue:51

    Topics: Amino Acid Sequence; Binding Sites; Clinical Trials as Topic; Drug Evaluation, Preclinical; Enzyme Stability; Humans; Molecular Sequence Data; Phylogeny; Protein Array Analysis; Protein Conformation; Protein Kinase Inhibitors; Protein Serine-Threonine Kinases

2007
Comparative structural and functional studies of 4-(thiazol-5-yl)-2-(phenylamino)pyrimidine-5-carbonitrile CDK9 inhibitors suggest the basis for isotype selectivity.
    Journal of medicinal chemistry, 2013, Feb-14, Volume: 56, Issue:3

    Topics: Cyclin-Dependent Kinase 9; Humans; Models, Molecular; Protein Kinase Inhibitors; Pyrimidines; Structure-Activity Relationship

2013
Rapid exchange of histone H1.1 on chromatin in living human cells.
    Nature, 2000, Dec-14, Volume: 408, Issue:6814

    Topics: Chromatin; Dichlororibofuranosylbenzimidazole; DNA; Enzyme Inhibitors; Green Fluorescent Proteins; Histones; Humans; Luminescent Proteins; Microscopy, Fluorescence; Phosphorylation; Protein Binding; Protein Kinase Inhibitors; Protein Kinases; Recombinant Fusion Proteins; Staurosporine; Tumor Cells, Cultured

2000
Phosphorylation of rat liver mitochondrial glycerol-3-phosphate acyltransferase by casein kinase 2.
    The Journal of biological chemistry, 2005, May-20, Volume: 280, Issue:20

    Topics: Amino Acid Sequence; Animals; Antibody Specificity; Binding Sites; Casein Kinase II; Dichlororibofuranosylbenzimidazole; Enzyme Inhibitors; Genistein; Glycerol-3-Phosphate O-Acyltransferase; Heparin; In Vitro Techniques; Male; Mitochondria, Liver; Molecular Weight; Phosphorus Radioisotopes; Phosphorylation; Rabbits; Rats; Rats, Sprague-Dawley; Staurosporine

2005