Page last updated: 2024-09-05

sb 203580 and ml 3403

sb 203580 has been researched along with ml 3403 in 4 studies

Compound Research Comparison

Studies
(sb 203580)
Trials
(sb 203580)
Recent Studies (post-2010)
(sb 203580)
Studies
(ml 3403)
Trials
(ml 3403)
Recent Studies (post-2010) (ml 3403)
3,48941,137502

Protein Interaction Comparison

ProteinTaxonomysb 203580 (IC50)ml 3403 (IC50)
Mitogen-activated protein kinase 13Homo sapiens (human)0.8538
Mitogen-activated protein kinase 12Homo sapiens (human)0.8538
Mitogen-activated protein kinase 11Homo sapiens (human)0.8538
Mitogen-activated protein kinase 14Homo sapiens (human)0.7748

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (75.00)29.6817
2010's1 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Albrecht, W; Kotschenreuther, DA; Laufer, SA; Wagner, GK1
Bullock, AN; Fedorov, O; Knapp, S; Marsden, B; Müller, S; Pogacic, V; Rellos, P; Schwaller, J; Sundström, M1
Domeyer, DM; Hauser, DR; Kinkel, K; Laufer, SA; Liedtke, AJ1
Augustin, M; Davies, SP; Gao, Y; Harvey, KJ; Kovelman, R; Patel, UA; Woodward, A1

Other Studies

4 other study(ies) available for sb 203580 and ml 3403

ArticleYear
Novel substituted pyridinyl imidazoles as potent anticytokine agents with low activity against hepatic cytochrome P450 enzymes.
    Journal of medicinal chemistry, 2003, Jul-17, Volume: 46, Issue:15

    Topics: Aminopyridines; Anti-Inflammatory Agents, Non-Steroidal; Chronic Disease; Cytochrome P-450 Enzyme System; Cytokines; Enzyme Inhibitors; Humans; Imidazoles; Interleukin-1; Isoenzymes; Leukocytes, Mononuclear; Liver; Mitogen-Activated Protein Kinases; Models, Molecular; p38 Mitogen-Activated Protein Kinases; Pyridines; Stereoisomerism; Structure-Activity Relationship; Tumor Necrosis Factor-alpha

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
Design, synthesis, and biological evaluation of novel Tri- and tetrasubstituted imidazoles as highly potent and specific ATP-mimetic inhibitors of p38 MAP kinase: focus on optimized interactions with the enzyme's surface-exposed front region.
    Journal of medicinal chemistry, 2008, Jul-24, Volume: 51, Issue:14

    Topics: Drug Design; Humans; Imidazoles; Molecular Mimicry; p38 Mitogen-Activated Protein Kinases; Protein Kinase Inhibitors; Structure-Activity Relationship

2008
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