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Results 1 - 10 of 13 > >>
EC Number
Inhibitors
Commentary
Structure
(2E)-2-[4-(dimethylamino)benzylidene]hydrazinecarboximidamide
binding affinity 0.030 mM
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(2E)-2-[[4-(dimethylamino)phenyl]methylidene]hydrazinecarboximidamide
binding affinity is 0.030 mM, complete inhibition
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(2Z)-4-[(4-anilinophenyl)amino]-4-oxobut-2-enoic acid
binding affinity 0.0201 mM, above 0.25 mM significant decrease in growth of strain on heme as sole source of iron
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(2Z)-N'-[(1Z)-pyridin-3-ylmethylene]-2-(pyridin-3-ylmethylene)hydrazinecarboximidohydrazide
binding affinity 0.0159 mM
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(2Z)-N'-[(1Z)-pyridin-3-ylmethylidene]-2-(pyridin-3-ylmethylidene)hydrazinecarboximidohydrazide
binding affinity is 0.0159 mM, complete inhibition
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1-(2,4-dinitrophenyl)methanamine
binding affinity 0.187 mM
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2-(4-chlorophenyl)-N'-[(1E)-1H-indol-3-ylmethylidene]acetohydrazide
binding affinity is 0.0158 mM, complete inhibition
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2-(4-chlorophenyl)-N'-[(1Z)-1H-inden-3-ylmethylene]acetohydrazide
binding affinity 0.0158 mM, above 0.25 mM significant decrease in growth of strain on heme as sole source of iron
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4-oxo-4-[[4-(phenylamino)phenyl]amino]butanoic acid
binding affinity is 0.0201 mM, complete inhibition
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4-[(2-hydroxyphenyl)amino]naphthalene-1,2-dione
binding affinity is 0.0728 mM, partial inhibition
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Results 1 - 10 of 13 > >>