Compounds > l 691831
Page last updated: 2024-09-03

l 691831 and mk 0591

l 691831 has been researched along with mk 0591 in 2 studies

Compound Research Comparison

Studies
(l 691831)		Trials
(l 691831)		Recent Studies (post-2010)
(l 691831)		Studies
(mk 0591)		Trials
(mk 0591)		Recent Studies (post-2010) (mk 0591)
50064617

Protein Interaction Comparison

ProteinTaxonomyl 691831 (IC50)mk 0591 (IC50)
Cytochrome P450 3A4Homo sapiens (human)2.6029
Polyunsaturated fatty acid 5-lipoxygenaseHomo sapiens (human)4.0003
Cytochrome P450 2D6Homo sapiens (human)0.011
Cytochrome P450 2C9 Homo sapiens (human)0.2503
Arachidonate 5-lipoxygenase-activating proteinHomo sapiens (human)0.0086

Research

Studies (2)

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

Authors

AuthorsStudies
Charleson, S; Evans, JF; Léger, S; Perrier, H; Prasit, P; Vickers, PJ; Wang, Z1
Brideau, C; Chan, CC; Falgueyret, JP; Frenette, R; Girard, Y; Guay, J; Hutchinson, JH; Macdonald, D; Perrier, H; Prasit, P; Riendeau, D; Tagari, P; Thérien, M; Young, RN1

Other Studies

2 other study(ies) available for l 691831 and mk 0591

ArticleYear
Structural requirements for the binding of fatty acids to 5-lipoxygenase-activating protein.
    European journal of pharmacology, 1994, May-17, Volume: 267, Issue:3

    Topics: 12-Hydroxy-5,8,10,14-eicosatetraenoic Acid; 5-Lipoxygenase-Activating Proteins; Arachidonic Acid; Binding Sites; Carrier Proteins; Humans; Hydroxyeicosatetraenoic Acids; Indoles; Leukocytes; Leukotrienes; Membrane Proteins; Quinolines; Radioligand Assay

1994
Substituted 2,2-bisaryl-bicycloheptanes as novel and potent inhibitors of 5-lipoxygenase activating protein.
    Bioorganic & medicinal chemistry letters, 2008, Mar-15, Volume: 18, Issue:6

    Topics: 5-Lipoxygenase-Activating Proteins; Ambrosia; Animals; Bridged Bicyclo Compounds; Carrier Proteins; Dogs; Heptanes; Humans; Indoles; Iodine Radioisotopes; Leukotriene D4; Lipoxygenase Inhibitors; Membrane Proteins; Molecular Structure; Neutrophils; Quinolines; Stereoisomerism; Structure-Activity Relationship

2008