Page last updated: 2024-09-05

sb 203580 and sb 216995

sb 203580 has been researched along with sb 216995 in 4 studies

Compound Research Comparison

Studies
(sb 203580)
Trials
(sb 203580)
Recent Studies (post-2010)
(sb 203580)
Studies
(sb 216995)
Trials
(sb 216995)
Recent Studies (post-2010) (sb 216995)
3,48941,137500

Protein Interaction Comparison

ProteinTaxonomysb 203580 (IC50)sb 216995 (IC50)
Chain A, MAP KINASE P38Homo sapiens (human)0.16
Chain A, PROTEIN (MAP KINASE P38)Homo sapiens (human)0.16
Chain A, PROTEIN (MAP KINASE P38)Homo sapiens (human)0.16
Chain A, Protein (map Kinase P38)Homo sapiens (human)0.16
Chain A, Extracellular Regulated Kinase 2Rattus norvegicus (Norway rat)0.16
Chain A, Extracellular Regulated Kinase 2Rattus norvegicus (Norway rat)0.16
Mitogen-activated protein kinase 13Homo sapiens (human)0.057
Mitogen-activated protein kinase 12Homo sapiens (human)0.057
Mitogen-activated protein kinase 1Rattus norvegicus (Norway rat)0.16
Mitogen-activated protein kinase 11Homo sapiens (human)0.057
Mitogen-activated protein kinase 14Homo sapiens (human)0.1188

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (50.00)18.2507
2000's1 (25.00)29.6817
2010's1 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Adams, JL; Badger, AM; Boehm, JC; Bradbeer, J; Breton, JJ; Chabot-Fletcher, MC; Gallagher, TF; Garigipati, RS; Griswold, DE; Hillegass, LM; Laydon, JT; Lee, JC; Sheldrake, PL; Smietana, JM; Sorenson, ME1
Abdel-Meguid, S; Adams, JL; Boehm, JC; Canagarajah, BJ; Cobb, MH; Goldsmith, EJ; Kassisà, S; Wang, Z; Young, PR1
Abadleh, M; Kinkel, K; Laufer, S; Peifer, C; Schollmeyer, D1
Barlow, DJ; Ehrman, TM; Hylands, PJ1

Other Studies

4 other study(ies) available for sb 203580 and sb 216995

ArticleYear
1-substituted 4-aryl-5-pyridinylimidazoles: a new class of cytokine suppressive drugs with low 5-lipoxygenase and cyclooxygenase inhibitory potency.
    Journal of medicinal chemistry, 1996, Sep-27, Volume: 39, Issue:20

    Topics: Animals; Anti-Inflammatory Agents, Non-Steroidal; Arachidonate 5-Lipoxygenase; Arachidonic Acid; Arthritis; Bone Density; Cyclooxygenase Inhibitors; Cytokines; Imidazoles; Lipoxygenase Inhibitors; Mice; Mice, Inbred BALB C; Molecular Structure; Morpholines; Prostaglandin-Endoperoxide Synthases; Protein Kinases; Rats; Structure-Activity Relationship; Tumor Necrosis Factor-alpha

1996
Structural basis of inhibitor selectivity in MAP kinases.
    Structure (London, England : 1993), 1998, Sep-15, Volume: 6, Issue:9

    Topics: Adenosine Triphosphate; Calcium-Calmodulin-Dependent Protein Kinases; Catalytic Domain; Cell Differentiation; Cell Division; Crystallography, X-Ray; Enzyme Inhibitors; Humans; Imidazoles; Kinetin; Mitogen-Activated Protein Kinase 1; Mitogen-Activated Protein Kinases; Models, Chemical; Models, Molecular; p38 Mitogen-Activated Protein Kinases; Protein Conformation; Purines; Pyridines; Pyrimidines; Structure-Activity Relationship

1998
From five- to six-membered rings: 3,4-diarylquinolinone as lead for novel p38MAP kinase inhibitors.
    Journal of medicinal chemistry, 2007, Mar-22, Volume: 50, Issue:6

    Topics: Binding Sites; Crystallography, X-Ray; Heterocyclic Compounds, 4 or More Rings; Mitogen-Activated Protein Kinase 10; Models, Molecular; p38 Mitogen-Activated Protein Kinases; Quinolones; Structure-Activity Relationship

2007
In silico search for multi-target anti-inflammatories in Chinese herbs and formulas.
    Bioorganic & medicinal chemistry, 2010, Mar-15, Volume: 18, Issue:6

    Topics: Anti-Inflammatory Agents; Crystallography, X-Ray; Cyclooxygenase 1; Cyclooxygenase 2; Databases, Factual; Drug Design; Drugs, Chinese Herbal; Enzyme Inhibitors; JNK Mitogen-Activated Protein Kinases; Medicine, Chinese Traditional; Models, Chemical; Models, Molecular; Molecular Conformation; p38 Mitogen-Activated Protein Kinases; Phosphodiesterase 4 Inhibitors; Structure-Activity Relationship

2010