Any feedback?
Please rate this page
(literature.php)
(0/150)

BRENDA support

Literature summary for 3.3.2.10 extracted from

  • Gurung, A.B.; Mayengbam, B.; Bhattacharjee, A.
    Discovery of novel drug candidates for inhibition of soluble epoxide hydrolase of arachidonic acid cascade pathway implicated in atherosclerosis (2018), Comput. Biol. Chem., 74, 1-11 .
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
(1Z)-1-[(4aS,8aR)-2-(3-[[(2S)-2-(5-methylfuran-2-yl)-2-(pyrrolidin-1-yl)ethyl]carbamoyl]phenyl)-4-oxooctahydrophthalazin-1(2H)-ylidene]dioxidan-1-ium
-
Homo sapiens
2-[(4-[3-[3-(pyridin-4-yl)-1,2,4-oxadiazol-5-yl]propanoyl]piperazin-1-yl)methyl]-4H-pyrido[1,2-a]pyrimidin-4-one
-
Homo sapiens
4-cyano-N-[(3S)-3-(4-fluorophenyl)-3-[4-(methanesulfonyl)phenyl]propyl]benzamide
-
Homo sapiens
4-[5-(cyclohexylamino)-2-(4-ethylpiperazin-1-yl)imidazo[2,1-b][1,3,4]thiadiazol-6-yl]-2,6-dimethoxyphenol
-
Homo sapiens
butyl 12-[[(adamantan-1-yl)carbamoyl]amino]dodecanoate
-
Homo sapiens
methyl 4-[(6R,12aS)-2-[3-(1H-imidazol-1-yl)propyl]-1,4-dioxo-1,2,3,4,6,7,12,12a-octahydropyrazino[1',2':1,6]pyrido[3,4-b]indol-6-yl]benzoate
-
Homo sapiens
additional information structural analysis of enzyme-inhibitor interactions, molecular interaction calculations, active site binding analysis, molecular docking, overview Homo sapiens
N-(3-methylphenyl)-4-[[1-methyl-5-(pyrrolidine-1-carbonyl)-1H-benzimidazol-2-yl]methyl]piperazine-1-carboxamide
-
Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens P34913
-
-

Synonyms

Synonyms Comment Organism
SEH
-
Homo sapiens

Temperature Optimum [°C]

Temperature Optimum [°C] Temperature Optimum Maximum [°C] Comment Organism
25
-
assay at Homo sapiens

pH Optimum

pH Optimum Minimum pH Optimum Maximum Comment Organism
7.5
-
assay at Homo sapiens