Page last updated: 2024-08-16

sk&f 86002 and birb 796

sk&f 86002 has been researched along with birb 796 in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (33.33)29.6817
2010's2 (66.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Churchill, L; Cirillo, PF; Gilmore, T; Graham, AG; Grob, PM; Hickey, ER; Moss, N; Pargellis, C; Pav, S; Regan, J; Tong, L1
Getlik, M; Grütter, C; Klüter, S; Naqvi, T; Pawar, V; Rabiller, M; Rauh, D; Simard, JR1
Davis, MI; Khan, J; Li, SQ; Patel, PR; Shen, M; Sun, H; Thomas, CJ1

Other Studies

3 other study(ies) available for sk&f 86002 and birb 796

ArticleYear
Inhibition of p38 MAP kinase by utilizing a novel allosteric binding site.
    Nature structural biology, 2002, Volume: 9, Issue:4

    Topics: Allosteric Site; Amino Acid Motifs; Cell Line; Crystallography, X-Ray; Enzyme Inhibitors; Humans; Inhibitory Concentration 50; Kinetics; Mitogen-Activated Protein Kinases; Models, Molecular; Naphthalenes; p38 Mitogen-Activated Protein Kinases; Protein Binding; Protein Conformation; Pyrazoles; Substrate Specificity; Time Factors

2002
Displacement assay for the detection of stabilizers of inactive kinase conformations.
    Journal of medicinal chemistry, 2010, Jan-14, Volume: 53, Issue:1

    Topics: Crystallography, X-Ray; Drug Design; Mitogen-Activated Protein Kinase 9; Models, Molecular; p38 Mitogen-Activated Protein Kinases; Protein Conformation; Protein Kinase Inhibitors; Pyrazoles; Structure-Activity Relationship; Urea

2010
Identification of potent Yes1 kinase inhibitors using a library screening approach.
    Bioorganic & medicinal chemistry letters, 2013, Aug-01, Volume: 23, Issue:15

    Topics: Binding Sites; Cell Line; Cell Survival; Drug Design; Humans; Hydrogen Bonding; Molecular Docking Simulation; Protein Kinase Inhibitors; Protein Structure, Tertiary; Proto-Oncogene Proteins c-yes; Small Molecule Libraries; Structure-Activity Relationship

2013