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

BRENDA support

Literature summary for 2.4.1.17 extracted from

  • Said, M.; Noort, D.; Magdalou, J.; Ziegler, J.C.; van der Marel, G.A.; van Boom, J.H.; Mulder, G.J.; Siest, G.
    Selective and potent inhibition of different hepatic UDP-glucuronosyltransferase activities by omega,omega,omega-triphenylalcohols and UDP derivatives (1992), Biochem. Biophys. Res. Commun., 187, 140-145.
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
7,7,7-triphenylheptyl-UDP
-
Rattus norvegicus
omega,omega,omega-triphenylalkyl-UDP derivatives e.g. 7,7,7-triphenylheptyl-UDP Rattus norvegicus

Localization

Localization Comment Organism GeneOntology No. Textmining
microsome
-
Rattus norvegicus
-
-

Organism

Organism UniProt Comment Textmining
Rattus norvegicus
-
Wistar strain
-
Rattus norvegicus Wistar
-
Wistar strain
-

Source Tissue

Source Tissue Comment Organism Textmining
liver
-
Rattus norvegicus
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
1-naphthol + UDP-glucuronate
-
Rattus norvegicus naphth-1-yl-beta-D-glucuronide + UDP
-
?
1-naphthol + UDP-glucuronate
-
Rattus norvegicus Wistar naphth-1-yl-beta-D-glucuronide + UDP
-
?

Ki Value [mM]

Ki Value [mM] Ki Value maximum [mM] Inhibitor Comment Organism Structure
0.03
-
7,7,7-triphenylheptyl-UDP apparent Ki for the inhibition of 1-naphthol glucuronidation Rattus norvegicus