Page last updated: 2024-09-03

mk 0663 and mf63 compound

mk 0663 has been researched along with mf63 compound in 1 studies

Compound Research Comparison

Studies
(mk 0663)
Trials
(mk 0663)
Recent Studies (post-2010)
(mk 0663)
Studies
(mf63 compound)
Trials
(mf63 compound)
Recent Studies (post-2010) (mf63 compound)
54917326523017

Protein Interaction Comparison

ProteinTaxonomymk 0663 (IC50)mf63 compound (IC50)
Prostaglandin E synthaseHomo sapiens (human)0.2006
Tyrosine-protein kinase JAK2Homo sapiens (human)0.1
Cytochrome P450 1A2Homo sapiens (human)0.0019
Cytochrome P450 2C9 Homo sapiens (human)0.0019
Thromboxane-A synthase Homo sapiens (human)3
Cytochrome P450 2C19Homo sapiens (human)0.0019
Glutathione transferase Sus scrofa (pig)0.0009

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Boulet, L; Brideau, C; Claveau, D; Côté, B; Ducharme, Y; Ethier, D; Frenette, R; Friesen, RW; Gagnon, M; Giroux, A; Guay, J; Guiral, S; Mancini, J; Martins, E; Massé, F; Méthot, N; Riendeau, D; Rubin, J; Xu, D; Yu, H1

Other Studies

1 other study(ies) available for mk 0663 and mf63 compound

ArticleYear
Substituted phenanthrene imidazoles as potent, selective, and orally active mPGES-1 inhibitors.
    Bioorganic & medicinal chemistry letters, 2007, Dec-15, Volume: 17, Issue:24

    Topics: Analgesics, Non-Narcotic; Animals; Disease Models, Animal; Drug Design; Guinea Pigs; Humans; Hyperalgesia; Imidazoles; Inhibitory Concentration 50; Intramolecular Oxidoreductases; Molecular Structure; Phenanthrenes; Prostaglandin-E Synthases; Rats; Structure-Activity Relationship

2007