Page last updated: 2024-08-23

staurosporine and sf 2370

staurosporine has been researched along with sf 2370 in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (40.00)18.2507
2000's1 (20.00)29.6817
2010's2 (40.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Davis, PD; Hill, CH; Hurst, SA; Keech, E; Lawton, G; Nixon, JS; Turner, SE; Wilkinson, SE1
Angeles, TS; Diebold, JL; Hudkins, RL; Knight, E1
Black, J; Fleming, M; Futer, O; Hare, B; Jacobs, MD; Saxena, K; Swenson, L1
Al-Mazaideh, GM; Erdmann, F; Göllner, C; Rohe, A; Schmidt, M; Sippl, W; Wichapong, K1
Augustin, M; Davies, SP; Gao, Y; Harvey, KJ; Kovelman, R; Patel, UA; Woodward, A1

Other Studies

5 other study(ies) available for staurosporine and sf 2370

ArticleYear
Inhibitors of protein kinase C. 1. 2,3-Bisarylmaleimides.
    Journal of medicinal chemistry, 1992, Volume: 35, Issue:1

    Topics: Animals; Binding Sites; Carbazoles; Cattle; Indoles; Maleimides; Protein Kinase Inhibitors; Rats; Structure-Activity Relationship

1992
Fused pyrrolo[2,3-c]carbazol-6-ones: novel immunostimulants that enhance human interferon-gamma activity.
    Journal of medicinal chemistry, 1997, Sep-12, Volume: 40, Issue:19

    Topics: Adjuvants, Immunologic; Carbazoles; Cell Line; Dimerization; Drug Synergism; Enzyme Inhibitors; HLA-DR Antigens; Humans; Indicators and Reagents; Interferon-gamma; Molecular Structure; Protein Kinase C; Pyrroles; Staurosporine; Structure-Activity Relationship

1997
Pim-1 ligand-bound structures reveal the mechanism of serine/threonine kinase inhibition by LY294002.
    The Journal of biological chemistry, 2005, Apr-08, Volume: 280, Issue:14

    Topics: Adenosine; Amino Acid Sequence; Binding Sites; Chromones; Cyclic AMP-Dependent Protein Kinases; Enzyme Inhibitors; Humans; Hydrogen Bonding; Ligands; Models, Molecular; Molecular Sequence Data; Molecular Structure; Morpholines; Phosphatidylinositol 3-Kinases; Protein Binding; Protein Conformation; Protein Serine-Threonine Kinases; Proto-Oncogene Proteins; Proto-Oncogene Proteins c-pim-1; Sequence Alignment; Staurosporine

2005
Evaluation of potential Myt1 kinase inhibitors by TR-FRET based binding assay.
    European journal of medicinal chemistry, 2013, Volume: 61

    Topics: Dose-Response Relationship, Drug; Fluorescence Resonance Energy Transfer; Glycolipids; Humans; Membrane Proteins; Models, Molecular; Molecular Structure; Protein Kinase Inhibitors; Protein Serine-Threonine Kinases; Protein-Tyrosine Kinases; Structure-Activity Relationship

2013
A broad activity screen in support of a chemogenomic map for kinase signalling research and drug discovery.
    The Biochemical journal, 2013, Apr-15, Volume: 451, Issue:2

    Topics: Aurora Kinases; Cluster Analysis; Drug Design; Drug Discovery; Drug Evaluation, Preclinical; ErbB Receptors; Humans; Intracellular Signaling Peptides and Proteins; MAP Kinase Kinase 4; p38 Mitogen-Activated Protein Kinases; Protein Kinase Inhibitors; Protein Kinases; Protein Serine-Threonine Kinases; Protein-Tyrosine Kinases; Receptors, Vascular Endothelial Growth Factor; Recombinant Proteins; Reproducibility of Results; Signal Transduction; Small Molecule Libraries; Structure-Activity Relationship; Syk Kinase

2013