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Found 83 with Last Name = 'paluszcak' and Initial = 'a'
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM9914(3-[(R)-1H-imidazol-1-yl(4-nitrophenyl)methyl]-4H-c...)
Affinity DataIC50:  2.30nMpH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta,2beta-3H]testosterone during aromatization. After incubation, the ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM9920((S)Fadrozole | 4-[(5S)-5,6,7,8-tetrahydroimidazo[1...)
Affinity DataIC50:  17nMpH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta,2beta-3H]testosterone during aromatization. After incubation, the ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM50191598(3-((1H-imidazol-1-yl)methyl)-2-(4-nitrophenyl)-4H-...)
Affinity DataIC50:  45nMAssay Description:Inhibition of CYP19More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM50191598(3-((1H-imidazol-1-yl)methyl)-2-(4-nitrophenyl)-4H-...)
Affinity DataIC50:  45nMAssay Description:Inhibition of CYP19More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM9916(3-[(R)-(4-bromophenyl)(1H-imidazol-1-yl)methyl]-4H...)
Affinity DataIC50:  49nMpH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta,2beta-3H]testosterone during aromatization. After incubation, the ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM9475(4-(1H-Imidazol-1-ylmethyl)-7-phenoxy-2H-chromen-2-...)
Affinity DataIC50:  51nMpH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta, 2beta-3H] testosterone or [1beta-3H] androstenedione during aroma...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)
Affinity DataIC50:  52nMAssay Description:Inhibition of CYP19More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM50191602(4'-cyano-3-(imidazolylmethyl)flavone | 4-(3-((1H-i...)
Affinity DataIC50:  69nMAssay Description:Inhibition of CYP19More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM50191602(4'-cyano-3-(imidazolylmethyl)flavone | 4-(3-((1H-i...)
Affinity DataIC50:  69nMAssay Description:Inhibition of CYP19More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM50191599(3-((1H-imidazol-1-yl)methyl)-2-phenyl-4H-chromen-4...)
Affinity DataIC50:  71nMAssay Description:Inhibition of CYP19More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM50191599(3-((1H-imidazol-1-yl)methyl)-2-phenyl-4H-chromen-4...)
Affinity DataIC50:  71nMAssay Description:Inhibition of CYP19More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM9465(1-(9-Phenyl-9H-fluoren-9-yl)-1H-imidazole | CHEMBL...)
Affinity DataIC50:  74nMpH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta, 2beta-3H] testosterone or [1beta-3H] androstenedione during aroma...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM50191600(3-((1H-imidazol-1-yl)methyl)-2-(4-methoxyphenyl)-4...)
Affinity DataIC50:  80nMAssay Description:Inhibition of CYP19More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM50191600(3-((1H-imidazol-1-yl)methyl)-2-(4-methoxyphenyl)-4...)
Affinity DataIC50:  80nMAssay Description:Inhibition of CYP19More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM9915(3-[(S)-1H-imidazol-1-yl(4-nitrophenyl)methyl]-4H-c...)
Affinity DataIC50:  96nMpH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta,2beta-3H]testosterone during aromatization. After incubation, the ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM9483(3-(1H-Imidazol-1-ylmethyl)-7-methoxy-4-phenyl-2H-c...)
Affinity DataIC50:  106nMpH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta, 2beta-3H] testosterone or [1beta-3H] androstenedione during aroma...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Homo sapiens (Human))
University Of Bari

LigandPNGBDBM8935(5-[(6-methoxy-1-methyl-3,4-dihydronaphthalen-2-yl)...)
Affinity DataIC50:  110nMAssay Description:The 17 alpha-hydroxylase activity of CYP 17 was determined by measuring the conversion of progesterone into 17 alpha-hydroxyprogesterone and the bypr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM9918(4-[(R)-1H-imidazol-1-yl(4-oxo-4H-chromen-3-yl)meth...)
Affinity DataIC50:  110nMpH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta,2beta-3H]testosterone during aromatization. After incubation, the ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM9477(6-(1H-Imidazol-1-ylmethyl)-2H-chromen-2-one | CHEM...)
Affinity DataIC50:  144nMpH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta, 2beta-3H] testosterone or [1beta-3H] androstenedione during aroma...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM9485(7-(benzyloxy)-4-(1H-imidazol-1-ylmethyl)-2H-chrome...)
Affinity DataIC50:  150nMpH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta, 2beta-3H] testosterone or [1beta-3H] androstenedione during aroma...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM9476(5-(1H-Imidazol-1-ylmethyl)-7-methoxy-2H-chromen-2-...)
Affinity DataIC50:  168nMpH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta, 2beta-3H] testosterone or [1beta-3H] androstenedione during aroma...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM9471(4-(1H-Imidazol-1-ylmethyl)-7-methoxy-2H-chromen-2-...)
Affinity DataIC50:  280nMpH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta, 2beta-3H] testosterone or [1beta-3H] androstenedione during aroma...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM9917(3-[(S)-(4-bromophenyl)(1H-imidazol-1-yl)methyl]-4H...)
Affinity DataIC50:  290nMpH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta,2beta-3H]testosterone during aromatization. After incubation, the ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM50191597(3-((1H-imidazol-1-yl)methyl)-2-(4-bromophenyl)-4H-...)
Affinity DataIC50:  440nMAssay Description:Inhibition of CYP19More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM50191597(3-((1H-imidazol-1-yl)methyl)-2-(4-bromophenyl)-4H-...)
Affinity DataIC50:  440nMAssay Description:Inhibition of CYP19More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM50191603(3-((1H-imidazol-1-yl)methyl)-7-methoxy-2-(4-nitrop...)
Affinity DataIC50:  468nMAssay Description:Inhibition of CYP19More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM50191603(3-((1H-imidazol-1-yl)methyl)-7-methoxy-2-(4-nitrop...)
Affinity DataIC50:  468nMAssay Description:Inhibition of CYP19More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM50097372(3-((1H-imidazol-1-yl)methyl)-7-methoxy-2-phenyl-4H...)
Affinity DataIC50:  550nMAssay Description:Inhibition of CYP19More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM50097372(3-((1H-imidazol-1-yl)methyl)-7-methoxy-2-phenyl-4H...)
Affinity DataIC50:  550nMAssay Description:Inhibition of CYP19More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM9919(4-[(S)-1H-imidazol-1-yl(4-oxo-4H-chromen-3-yl)meth...)
Affinity DataIC50:  630nMpH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta,2beta-3H]testosterone during aromatization. After incubation, the ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM9478(7-(1H-Imidazol-1-ylmethyl)-2H-chromen-2-one | CHEM...)
Affinity DataIC50:  680nMpH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta, 2beta-3H] testosterone or [1beta-3H] androstenedione during aroma...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM9473(4-[2-(1H-Imidazol-1-yl)ethoxy]-2H-chromen-2-one | ...)
Affinity DataIC50:  760nMpH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta, 2beta-3H] testosterone or [1beta-3H] androstenedione during aroma...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM9486(6-(1H-Imidazol-1-ylmethyl)-2H-chrome-2-thione | 6-...)
Affinity DataIC50:  1.13E+3nMpH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta, 2beta-3H] testosterone or [1beta-3H] androstenedione during aroma...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM50191601(4'-cyano-3-(imidazolylmethyl)-7-methoxyflavone | 4...)
Affinity DataIC50:  1.82E+3nMAssay Description:Inhibition of CYP19More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM50191601(4'-cyano-3-(imidazolylmethyl)-7-methoxyflavone | 4...)
Affinity DataIC50:  1.82E+3nMAssay Description:Inhibition of CYP19More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM9470(4-(1H-Imidazol-1-ylmethyl)-2H-chromen-2-one | CHEM...)
Affinity DataIC50:  2.10E+3nMpH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta, 2beta-3H] testosterone or [1beta-3H] androstenedione during aroma...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM9469(3-(1H-Imidazol-1-ylmethyl)-7-methoxy-2H-chromen-2-...)
Affinity DataIC50:  2.82E+3nMpH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta, 2beta-3H] testosterone or [1beta-3H] androstenedione during aroma...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM9462(1-{2-methyl-5H-indeno[1,2-d]pyrimidin-5-yl}-1H-imi...)
Affinity DataIC50:  2.85E+3nMpH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta, 2beta-3H] testosterone or [1beta-3H] androstenedione during aroma...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM9464(1-(9H-Fluoren-9-yl)-1H-imidazole | CHEMBL225447 | ...)
Affinity DataIC50:  2.85E+3nMpH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta, 2beta-3H] testosterone or [1beta-3H] androstenedione during aroma...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM9472(7-Methoxy-4-(1H-1,2,4-triazol-1-ylmethyl)-2H-chrom...)
Affinity DataIC50:  3.60E+3nMpH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta, 2beta-3H] testosterone or [1beta-3H] androstenedione during aroma...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM9468(1-(9-Phenyl-9H-fluoren-9-yl)-1H-1,2,4-triazole | C...)
Affinity DataIC50:  4.00E+3nMpH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta, 2beta-3H] testosterone or [1beta-3H] androstenedione during aroma...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM50191596(3-((1H-imidazol-1-yl)methyl)-2-(4-bromophenyl)-7-m...)
Affinity DataIC50:  4.07E+3nMAssay Description:Inhibition of CYP19More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM50191596(3-((1H-imidazol-1-yl)methyl)-2-(4-bromophenyl)-7-m...)
Affinity DataIC50:  4.07E+3nMAssay Description:Inhibition of CYP19More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM9482(4-(1H-Imidazol-1-ylmethyl)-3-phenyl-2H-chromen-2-o...)
Affinity DataIC50:  5.13E+3nMpH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta, 2beta-3H] testosterone or [1beta-3H] androstenedione during aroma...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM8935(5-[(6-methoxy-1-methyl-3,4-dihydronaphthalen-2-yl)...)
Affinity DataIC50:  1.70E+4nMpH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta, 2beta-3H] testosterone or [1beta-3H] androstenedione during aroma...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM9463(3-(1H-Imidazol-1-ylmethyl)-5H-indeno[1,2-c]pyridaz...)
Affinity DataIC50:  2.66E+4nMpH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta, 2beta-3H] testosterone or [1beta-3H] androstenedione during aroma...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Homo sapiens (Human))
University Of Bari

LigandPNGBDBM9463(3-(1H-Imidazol-1-ylmethyl)-5H-indeno[1,2-c]pyridaz...)
Affinity DataAssay Description:The 17 alpha-hydroxylase activity of CYP 17 was determined by measuring the conversion of progesterone into 17 alpha-hydroxyprogesterone and the bypr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Homo sapiens (Human))
University Of Bari

LigandPNGBDBM9465(1-(9-Phenyl-9H-fluoren-9-yl)-1H-imidazole | CHEMBL...)
Affinity DataAssay Description:The 17 alpha-hydroxylase activity of CYP 17 was determined by measuring the conversion of progesterone into 17 alpha-hydroxyprogesterone and the bypr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Homo sapiens (Human))
University Of Bari

LigandPNGBDBM9466(4-(9-Phenyl-9H-fluoren-9-yl)-4H-1,2,4-triazole | F...)
Affinity DataAssay Description:The 17 alpha-hydroxylase activity of CYP 17 was determined by measuring the conversion of progesterone into 17 alpha-hydroxyprogesterone and the bypr...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Homo sapiens (Human))
University Of Bari

LigandPNGBDBM9467(1-(9-Phenyl-9H-fluoren-9-yl)-1H-1,2,3-triazole | F...)
Affinity DataAssay Description:The 17 alpha-hydroxylase activity of CYP 17 was determined by measuring the conversion of progesterone into 17 alpha-hydroxyprogesterone and the bypr...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
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