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Results 1 - 10 of 104 > >>
EC Number
Inhibitors
Commentary
Structure
2,2,6,6-tetramethylpiperidinyl-1-oxide
formation of 2,2,6,6-tetramethylpiperidinyl-1-oxy-adducts and subsequent oxidation of the cysteine residue located near the propionate group of heme leads to loss of enzyme activity
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2,2,6,6-tetramethylpiperidinyl-1-oxyl radical
formation of 2,2,6,6-tetramethylpiperidinyl-1-oxy-adducts and subsequent oxidation of the cysteine residue located near the propionate group of heme leads to loss of enzyme activity
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2,6-dichloroisonicotinic acid
54% inhibition at 0.1 mM, 95% inhibition at 1 mM, the inhibition is not time-dependent
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2,6-dihydroxybenzoic acid
biologically active, 72% inhibition at 0.2 mM
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2-mercaptoethanol
enzyme form C: 50% inhibition at 5 mM, 6 min, 100% inhibition after 18 min
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2-mercaptoethanol
not inhibitory at 0.5 mM, 31% inhibition at 5 mM
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3,3'-dithiobis(6-nitrobenzoic acid)
5 mM, 80% residual activity, APX 1, 24% residual activity, APX 2
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3,5-dichlorosalicylic acid
biologically active, 59% inhibition at 0.2 mM
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3-Hydroxybenzoic acid
biologically inactive, 28% inhibition at 0.2 mM
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4-aminosalicylic acid
biologically inactive, 9% inhibition at 0.2 mM
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Results 1 - 10 of 104 > >>