Page last updated: 2024-09-05

sb 203580 and rwj 68354

sb 203580 has been researched along with rwj 68354 in 3 studies

Compound Research Comparison

Studies
(sb 203580)
Trials
(sb 203580)
Recent Studies (post-2010)
(sb 203580)
Studies
(rwj 68354)
Trials
(rwj 68354)
Recent Studies (post-2010) (rwj 68354)
3,48941,137500

Protein Interaction Comparison

ProteinTaxonomysb 203580 (IC50)rwj 68354 (IC50)
Mitogen-activated protein kinase 13Homo sapiens (human)0.0067
5-hydroxytryptamine receptor 4Cavia porcellus (domestic guinea pig)1.237
Aldo-keto reductase family 1 member B1Rattus norvegicus (Norway rat)1.07
Neutrophil elastaseHomo sapiens (human)0.0063
Cytochrome P450 3A4Homo sapiens (human)1
Cytochrome P450 2D6Homo sapiens (human)0.2
Cytochrome P450 2C9 Homo sapiens (human)1
Sodium-dependent noradrenaline transporter Homo sapiens (human)1.07
5-hydroxytryptamine receptor 2CHomo sapiens (human)1.237
Adenosine receptor A2aHomo sapiens (human)1.032
Adenosine receptor A1Homo sapiens (human)0.887
Mitogen-activated protein kinase 14 Mus musculus (house mouse)1.5
Mitogen-activated protein kinase 12Homo sapiens (human)0.0067
Mitogen-activated protein kinase 11Homo sapiens (human)0.0067
Mitogen-activated protein kinase 14Homo sapiens (human)0.0385

Research

Studies (3)

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

Authors

AuthorsStudies
Cavender, DE; Davis, JE; Dodd, JH; Fahmy, B; Henry, JR; Olini, GC; Pellegrino-Gensey, JL; Rupert, KC; Schafer, PH; Siekierka, JJ; Turchi, IJ; Wadsworth, SA1
Cavender, DE; Dodd, JH; Henry, JR; Rupert, KC; Schafer, PH; Siekierka, JJ; Turchi, IJ; Wadsworth, SA1
Barberia, JT; Carty, TJ; Cortina, SR; Csiki, C; Dipesa, AJ; Dombroski, MA; Elliott, NC; Gabel, CA; Jordan, CK; Labasi, JM; Letavic, MA; Martin, WH; McClure, KF; Peese, KM; Stock, IA; Svensson, L; Sweeney, FJ; Yu, CH1

Other Studies

3 other study(ies) available for sb 203580 and rwj 68354

ArticleYear
6-Amino-2-(4-fluorophenyl)-4-methoxy-3- (4-pyridyl)-1H-pyrrolo[2, 3-b]pyridine (RWJ 68354): a potent and selective p38 kinase inhibitor.
    Journal of medicinal chemistry, 1998, Oct-22, Volume: 41, Issue:22

    Topics: Aminopyridines; Animals; Arthritis, Experimental; Calcium-Calmodulin-Dependent Protein Kinases; Enzyme Inhibitors; Humans; In Vitro Techniques; Interleukin-1; Lipopolysaccharides; Male; Mice; Mice, Inbred BALB C; Mitogen-Activated Protein Kinases; Monocytes; p38 Mitogen-Activated Protein Kinases; Pyrroles; Rats; Rats, Inbred Lew; T-Lymphocytes; Tumor Necrosis Factor-alpha

1998
Potent inhibitors of the MAP kinase p38.
    Bioorganic & medicinal chemistry letters, 1998, Dec-01, Volume: 8, Issue:23

    Topics: Anti-Inflammatory Agents; Calcium-Calmodulin-Dependent Protein Kinases; Enzyme Inhibitors; Humans; Imidazoles; Intracellular Signaling Peptides and Proteins; Lipopolysaccharides; Mitogen-Activated Protein Kinases; p38 Mitogen-Activated Protein Kinases; Protein Serine-Threonine Kinases; Pyridines; Tumor Necrosis Factor-alpha

1998
Benzimidazolone p38 inhibitors.
    Bioorganic & medicinal chemistry letters, 2004, Feb-23, Volume: 14, Issue:4

    Topics: Benzimidazoles; Enzyme Inhibitors; Imidazoles; Mitogen-Activated Protein Kinase 14; Mitogen-Activated Protein Kinases; Molecular Structure; Pyridines; Structure-Activity Relationship

2004