Inhibitors | Comment | Organism | Structure |
---|---|---|---|
4-[5-(1H-indol-3-yl)-3-trifluoromethyl-4,5-dihydropyrazol-1-yl]-benzenesulfonamide | 0.01 mM inhibits LOX-12 by 5% | Homo sapiens | |
4-[5-(7-chloro-1H-indol-3-yl)-3-trifluoromethyl-4,5-dihydropyrazol-1-yl]-benzenesulfonamide | 0.01 mM inhibits LOX-12 by 3% | Homo sapiens | |
celecoxib | 0.01 mM inhibits LOX-12 by 7% | Homo sapiens | |
additional information | 0.01 mM 4-[5-(6-chloro-1H-indol-3-yl)-3-trifluoromethyl-4,5-dihydropyrazol-1-yl]-benzenesulfonamide or rofecoxib do not inhibit LOX-12 | Homo sapiens |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Homo sapiens | - |
- |
- |
Source Tissue | Comment | Organism | Textmining |
---|---|---|---|
blood platelet | - |
Homo sapiens | - |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
arachidonate + O2 | - |
Homo sapiens | (5Z,8Z,10E,14Z)-(12S)-12-hydroperoxyicosa-5,8,10,14-tetraenoate | - |
? | |
linoleate + O2 | - |
Homo sapiens | (9Z,11E)-(13S)-13-hydroperoxyoctadeca-9,11-dienoate | - |
? |
Synonyms | Comment | Organism |
---|---|---|
lipoxygenase 12 | - |
Homo sapiens |
LOX-12 | - |
Homo sapiens |