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Literature summary for 1.11.2.2 extracted from

  • Shiba, Y.; Kinoshita, T.; Chuman, H.; Taketani, Y.; Takeda, E.; Kato, Y.; Naito, M.; Kawabata, K.; Ishisaka, A.; Terao, J.; Kawai, Y.
    Flavonoids as substrates and inhibitors of myeloperoxidase: molecular actions of aglycone and metabolites (2008), Chem. Res. Toxicol., 21, 1600-1609.
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
dityrosine inhibits MPO-derived dityrosine formation in a dose-dependent manner Homo sapiens
fisetin
-
Homo sapiens
kaempferol
-
Homo sapiens
luteolin
-
Homo sapiens
myricetin
-
Homo sapiens
Q3GA inhibits MPO-derived dityrosine formation in a dose-dependent manner Homo sapiens
quercetin potent inhibitor, inhibits MPO-derived dityrosine formation in a dose-dependent manner Homo sapiens
taxifolin
-
Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens P05164
-
-

Source Tissue

Source Tissue Comment Organism Textmining
aorta atherosclerotic aorta Homo sapiens
-
HL-60 cell
-
Homo sapiens
-
macrophage
-
Homo sapiens
-
sputum
-
Homo sapiens
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
quercetin + H2O2
-
Homo sapiens oxidized quercetin + H2O
-
?
tyrosine + H2O2
-
Homo sapiens dityrosine + H2O
-
?

Synonyms

Synonyms Comment Organism
MPO
-
Homo sapiens
myeloperoxidase
-
Homo sapiens

IC50 Value

IC50 Value IC50 Value Maximum Comment Organism Inhibitor Structure
0.00127
-
-
Homo sapiens quercetin
0.00208
-
-
Homo sapiens kaempferol
0.00387
-
-
Homo sapiens fisetin
0.00422
-
-
Homo sapiens luteolin
0.00663
-
-
Homo sapiens taxifolin