Page last updated: 2024-09-03

bay x 1005 and 5-hydroxy-6,8,11,14-eicosatetraenoic acid

bay x 1005 has been researched along with 5-hydroxy-6,8,11,14-eicosatetraenoic acid in 1 studies

Compound Research Comparison

Studies
(bay x 1005)
Trials
(bay x 1005)
Recent Studies (post-2010)
(bay x 1005)
Studies
(5-hydroxy-6,8,11,14-eicosatetraenoic acid)
Trials
(5-hydroxy-6,8,11,14-eicosatetraenoic acid)
Recent Studies (post-2010) (5-hydroxy-6,8,11,14-eicosatetraenoic acid)
5868648554

Protein Interaction Comparison

ProteinTaxonomybay x 1005 (IC50)5-hydroxy-6,8,11,14-eicosatetraenoic acid (IC50)
Polyunsaturated fatty acid 5-lipoxygenaseHomo sapiens (human)2

Research

Studies (1)

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

Authors

AuthorsStudies
Fruchtmann, R; Hatzelmann, A; Mohrs, KH; Müller-Peddinghaus, R; Raddatz, S1

Other Studies

1 other study(ies) available for bay x 1005 and 5-hydroxy-6,8,11,14-eicosatetraenoic acid

ArticleYear
Mode of action of the new selective leukotriene synthesis inhibitor BAY X 1005 ((R)-2-[4-(quinolin-2-yl-methoxy)phenyl]-2-cyclopentyl acetic acid) and structurally related compounds.
    Biochemical pharmacology, 1993, Jan-07, Volume: 45, Issue:1

    Topics: Animals; Arachidonic Acid; Binding Sites; Binding, Competitive; Cell-Free System; Humans; Hydroxyeicosatetraenoic Acids; Indoles; Kinetics; Leukotriene B4; Lipoxygenase Inhibitors; Neutrophils; Platelet Activating Factor; Quinolines; Rats; Structure-Activity Relationship; Subcellular Fractions

1993