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Literature summary extracted from

  • Poirot, M.; Silvente-Poirot, S.
    Cholesterol-5,6-epoxides: chemistry, biochemistry, metabolic fate and cancer (2013), Biochimie, 95, 622-631.
    View publication on PubMed

Inhibitors

EC Number Inhibitors Comment Organism Structure
3.3.2.11 tamoxifen
-
Rattus norvegicus

Natural Substrates/ Products (Substrates)

EC Number Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
3.3.2.11 5,6alpha-epoxy-5alpha-cholestan-3beta-ol + H2O Rattus norvegicus
-
5alpha-cholestane-3beta,5alpha,6beta-triol
-
?
3.3.2.11 5,6beta-epoxy-5alpha-cholestan-3beta-ol + H2O Rattus norvegicus best substrate 5alpha-cholestane-3beta,5alpha,6beta-triol
-
?

Organism

EC Number Organism UniProt Comment Textmining
3.3.2.11 Rattus norvegicus
-
-
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
3.3.2.11 5,6alpha-epoxy-5alpha-cholestan-3beta-ol + H2O
-
Rattus norvegicus 5alpha-cholestane-3beta,5alpha,6beta-triol
-
?
3.3.2.11 5,6beta-epoxy-5alpha-cholestan-3beta-ol + H2O best substrate Rattus norvegicus 5alpha-cholestane-3beta,5alpha,6beta-triol
-
?

Synonyms

EC Number Synonyms Comment Organism
3.3.2.11 ChEH
-
Rattus norvegicus
3.3.2.11 cholesterol-5,6-epoxide hydrolase
-
Rattus norvegicus

General Information

EC Number General Information Comment Organism
3.3.2.11 physiological function primary and secondary products of the enzyme's activity have tumor promoting and carcinogenic activity Rattus norvegicus