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Literature summary extracted from

  • Tai, H.H.; Yuan, B.
    On the inhibitory potency of imidazole and its derivatives on thromboxane synthetase (1978), Biochem. Biophys. Res. Commun., 80, 236-242.
    View publication on PubMed

Inhibitors

EC Number Inhibitors Comment Organism Structure
5.3.99.5 1-(2-Isopropylphenyl)-imidazole strong Homo sapiens
5.3.99.5 1-Decylimidazole strong Homo sapiens
5.3.99.5 1-Nonylimidazole strong Homo sapiens
5.3.99.5 imidazole and derivatives. The potency of 1-substituted imidazoles is increased as the side chain becomes more hydrophobic. Inhibition is competitive with respect to prostaglandin endoperoxide substrate Homo sapiens

Localization

EC Number Localization Comment Organism GeneOntology No. Textmining
5.3.99.5 microsome
-
Homo sapiens
-
-

Organism

EC Number Organism UniProt Comment Textmining
5.3.99.5 Homo sapiens
-
-
-

Source Tissue

EC Number Source Tissue Comment Organism Textmining
5.3.99.5 platelet
-
Homo sapiens
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
5.3.99.5 Prostaglandin H2 i.e. PGH2 Homo sapiens thromboxane B2 + 12(L)-hydroxy-5,8,10-heptadecatrienoic acid
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