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Literature summary for 3.3.2.10 extracted from

  • Revermann, M.
    Pharmacological inhibition of the soluble epoxide hydrolase-from mouse to man (2010), Curr. Opin. Pharmacol., 10, 173-178.
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
additional information sEH inhibitors are 1,3-disubstituted ureas, amides and carbamates that have IC50-values in the low nanomolar range. They only block the hydrolase activity of the enzyme without affecting the phosphatase domain Mammalia

Localization

Localization Comment Organism GeneOntology No. Textmining
soluble
-
Mammalia
-
-

Molecular Weight [Da]

Molecular Weight [Da] Molecular Weight Maximum [Da] Comment Organism
62000
-
2 * 62000 Mammalia

Organism

Organism UniProt Comment Textmining
Mammalia
-
-
-

Source Tissue

Source Tissue Comment Organism Textmining
heart
-
Mammalia
-
kidney
-
Mammalia
-
additional information sEH is ubiquituously expressed Mammalia
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
additional information the enzyme possesses an epoxide hydrolyzing as well as a lipid phosphatase activity. Favored sEH substrates are trans-substituted over cis-substituted epoxides Mammalia ?
-
?

Subunits

Subunits Comment Organism
homodimer 2 * 62000 Mammalia

Synonyms

Synonyms Comment Organism
SEH
-
Mammalia

General Information

General Information Comment Organism
additional information sEh inhibition reduces inflammation. In several mouse models, sEH inhibition reduces atherosclerosis and aortic aneurysm formation. The anti-proliferative effect of urea-based sEH inhibitors is probably caused by PPARa activation and consecutive inhibition of cyclin D1 expression. And sEH inhibition affects renal fucntions, overview Mammalia
physiological function sEH is not essentially involved in the metabolization and clearance of carcinogenic xenobiotics. But sEH is involved in inflammation Mammalia