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Results 1 - 10 of 70 > >>
EC Number
Inhibitors
Commentary
Structure
1,5-dihydrofuro[3,4-d]pyrimidine-2,4,7-trione
-
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1-(1-naphthyl)-3-[2-(trifluoromethyl)phenyl]urea
50% inhibition at 0.0004 mM, wild type, 0.00034 mM, mutant R265A, above 0.2, mutant H185A
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1-(2-methoxyphenyl)-3-(1-naphthyl)urea
50% inhibition at 0.00023 mM, wild type, 0.00024 mM, mutant R265A, 0.140, mutant H185A
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1-(4-Chloro-phenyl)-1H-pyrazole-3,5-dicarboxylic acid 3-(4-methyl-benzylamide) 5-phenylamide
; minimum inhibitory concentration 0.032 mg/ml
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1-(4-Chloro-phenyl)-1H-pyrazole-3,5-dicarboxylic acid 3-benzylamide 5-(isobutyl-amide)
; minimum inhibitory concentration above 0.064 mg/ml
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1-(4-Chloro-phenyl)-1H-pyrazole-3,5-dicarboxylic acid 3-benzylamide 5-[(4-carbamoyl-phenyl)-amide]
; minimum inhibitory concentration 0.008 mg/ml
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1-(4-Chloro-phenyl)-1H-pyrazole-3,5-dicarboxylic acid 5-phenylamide 3-[(pyridin-3-ylmethyl)-amide]
; minimum inhibitory concentration 0.00025 mg/ml
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1-(4-Chloro-phenyl)-1H-pyrazole-3,5-dicarboxylic acid 5-[(4-piperidin-1-yl-phenyl)-amide] 3-[(pyridin-3-ylmethyl)-amide]
; minimum inhibitory concentration 0.002 mg/ml
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1-(4-chlorophenyl)-3-quinolin-8-ylurea
50% inhibition at 0.00078 mM, wild type, 0.002 mM, mutant R265A, above 0.4, mutant H185A
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1-(4-Methoxy-phenyl)-1H-pyrazole-3,5-dicarboxylic acid 3-(isobutyl-amide) 5-[[4-(pyrrolidine-1-carbonyl)-phenyl]-amide]
; minimum inhibitory concentration 0.064 mg/ml
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Results 1 - 10 of 70 > >>