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Literature summary for 1.14.99.1 extracted from

  • Forghani, F.; Ouellet, M.; Keen, S.; Percival, M.D.; Tagari, P.
    Analysis of prostaglandin G/H synthase-2 inhibition using peroxidase-induced luminol luminescence (1998), Anal. Biochem., 264, 216-221.
    View publication on PubMed

Application

Application Comment Organism
medicine use of peroxidase activity for luminol assay of inflammation Homo sapiens

Inhibitors

Inhibitors Comment Organism Structure
5-bromo-2-[4-fluorophenyl]-3-[4-methylsulfonylphenyl]-thiophene 50% inhibition at 8.7 nM Homo sapiens
diclofenac 50% inhibition at 9.4 nM Homo sapiens
flosulide selective for isozyme 2, 50% inhibition at 130 nM Homo sapiens
Flufenamic acid 50% inhibition at 0.02 mM Homo sapiens
Ibuprofen 50% inhibition at 0.253 mM Homo sapiens
indomethacin 50% inhibition at 100 nM Homo sapiens
N-[2-cyclohexyloxy-4-nitrophenyl]methanesulfonamide 50% inhibition at 81 nM Homo sapiens

KM Value [mM]

KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
0.006
-
arachidonic acid
-
Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens
-
recombinant enzyme, product of COX-2
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
arachidonate + electron donor + O2
-
Homo sapiens prostaglandin H2 + oxidized electron donor + H2O
-
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