Compile Data Set for Download or QSAR
Report error Found 50 Enz. Inhib. hit(s) with all data for entry = 1161
TargetAromatase(Human)
University of Bari

LigandPNGBDBM9479(7-(1H-1,2,4-Triazol-1-ylmethyl)-2H-chromen-2-one |...)
Affinity DatapH: 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 Article
PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
University of Bari

LigandPNGBDBM9470(CHEMBL427247 | 4-(1H-Imidazol-1-ylmethyl)-2H-chrom...)
Affinity DataAssay 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 Article
PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
University of Bari

LigandPNGBDBM9469(CHEMBL387892 | 3-(1H-Imidazol-1-ylmethyl)-7-methox...)
Affinity DataAssay 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 Article
PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
University of Bari

LigandPNGBDBM9468(CHEMBL376371 | 1-(9-Phenyl-9H-fluoren-9-yl)-1H-1,2...)
Affinity DataAssay 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 Article
PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
University of Bari

LigandPNGBDBM9467(1-(9-Phenyl-9H-fluoren-9-yl)-1H-1,2,3-triazole | F...)
Affinity DataAssay 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 Article
PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
University of Bari

LigandPNGBDBM9466(4-(9-Phenyl-9H-fluoren-9-yl)-4H-1,2,4-triazole | F...)
Affinity DataAssay 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 Article
PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
University of Bari

LigandPNGBDBM9465(1-(9-Phenyl-9H-fluoren-9-yl)-1H-imidazole | CHEMBL...)
Affinity DataAssay 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 Article
PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
University of Bari

LigandPNGBDBM9463(3-(1H-Imidazol-1-ylmethyl)-5H-indeno[1,2-c]pyridaz...)
Affinity DataAssay 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 Article
PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
University of Bari

LigandPNGBDBM9462(5-(1H-Imidazol-1-yl)-2-methyl-5H-indeno[1,2-d]pyri...)
Affinity DataAssay 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 Article
PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
University of Bari

LigandPNGBDBM9471(4-(1H-Imidazol-1-ylmethyl)-7-methoxy-2H-chromen-2-...)
Affinity DataAssay 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 Article
PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
University of Bari

LigandPNGBDBM9472(CHEMBL388604 | 7-Methoxy-4-(1H-1,2,4-triazol-1-ylm...)
Affinity DataAssay 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 Article
PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
University of Bari

LigandPNGBDBM9473(CHEMBL225178 | 4-[2-(1H-Imidazol-1-yl)ethoxy]-2H-c...)
Affinity DataAssay 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 Article
PubMed
TargetAromatase(Human)
University of Bari

LigandPNGBDBM9484(7-methoxy-4-(pyridin-4-yl)-2H-chromen-2-one | Coum...)
Affinity DatapH: 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 Article
PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
University of Bari

LigandPNGBDBM9475(4-(1H-Imidazol-1-ylmethyl)-7-phenoxy-2H-chromen-2-...)
Affinity DataAssay 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 Article
PubMed
TargetAromatase(Human)
University of Bari

LigandPNGBDBM9481(8-(1H-Imidazol-1-ylmethyl)-7-methoxy-2H-chromen-2-...)
Affinity DatapH: 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 Article
PubMed
TargetAromatase(Human)
University of Bari

LigandPNGBDBM9480(7-[2-(1H-Imidazol-1-yl)ethoxy]-2H-chromen-2-one | ...)
Affinity DatapH: 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 Article
PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
University of Bari

LigandPNGBDBM9481(8-(1H-Imidazol-1-ylmethyl)-7-methoxy-2H-chromen-2-...)
Affinity DataAssay 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 Article
PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
University of Bari

LigandPNGBDBM9486(6-(1H-imidazol-1-ylmethyl)-2H-chromene-2-thione | ...)
Affinity DataAssay 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 Article
PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
University of Bari

LigandPNGBDBM9485(7-(benzyloxy)-4-(1H-imidazol-1-ylmethyl)-2H-chrome...)
Affinity DataAssay 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 Article
PubMed
TargetAromatase(Human)
University of Bari

LigandPNGBDBM9466(4-(9-Phenyl-9H-fluoren-9-yl)-4H-1,2,4-triazole | F...)
Affinity DatapH: 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 Article
PubMed
TargetAromatase(Human)
University of Bari

LigandPNGBDBM9467(1-(9-Phenyl-9H-fluoren-9-yl)-1H-1,2,3-triazole | F...)
Affinity DatapH: 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 Article
PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
University of Bari

LigandPNGBDBM9484(7-methoxy-4-(pyridin-4-yl)-2H-chromen-2-one | Coum...)
Affinity DataAssay 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 Article
PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
University of Bari

LigandPNGBDBM9483(CHEMBL224787 | 3-(1H-Imidazol-1-ylmethyl)-7-methox...)
Affinity DataAssay 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 Article
PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
University of Bari

LigandPNGBDBM9482(CHEMBL224786 | 4-(1H-Imidazol-1-ylmethyl)-3-phenyl...)
Affinity DataAssay 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 Article
PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
University of Bari

LigandPNGBDBM9476(5-(1H-Imidazol-1-ylmethyl)-7-methoxy-2H-chromen-2-...)
Affinity DataAssay 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 Article
PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
University of Bari

LigandPNGBDBM9480(7-[2-(1H-Imidazol-1-yl)ethoxy]-2H-chromen-2-one | ...)
Affinity DataAssay 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 Article
PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
University of Bari

LigandPNGBDBM9479(7-(1H-1,2,4-Triazol-1-ylmethyl)-2H-chromen-2-one |...)
Affinity DataAssay 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 Article
PubMed
TargetAromatase(Human)
University of Bari

LigandPNGBDBM9474(4-[2-(1H-Imidazol-1-yl)ethoxy]-7-methoxy-2H-chrome...)
Affinity DatapH: 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 Article
PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
University of Bari

LigandPNGBDBM9478(CHEMBL224649 | 7-(1H-Imidazol-1-ylmethyl)-2H-chrom...)
Affinity DataAssay 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 Article
PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
University of Bari

LigandPNGBDBM9477(CHEMBL224228 | 6-(1H-Imidazol-1-ylmethyl)-2H-chrom...)
Affinity DataAssay 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 Article
PubMed
TargetAromatase(Human)
University of Bari

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 Article
PubMed
TargetAromatase(Human)
University of Bari

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 Article
PubMed
TargetAromatase(Human)
University of Bari

LigandPNGBDBM9483(CHEMBL224787 | 3-(1H-Imidazol-1-ylmethyl)-7-methox...)
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 Article
PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
University of Bari

LigandPNGBDBM8935(CHEMBL448463 | dihydronaphthalene derivative | 5-[...)
Affinity DataIC50: 110nMAssay 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 Article
PubMed
TargetAromatase(Human)
University of Bari

LigandPNGBDBM9477(CHEMBL224228 | 6-(1H-Imidazol-1-ylmethyl)-2H-chrom...)
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 Article
PubMed
TargetAromatase(Human)
University of Bari

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 Article
PubMed
TargetAromatase(Human)
University of Bari

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 Article
PubMed
TargetAromatase(Human)
University of Bari

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 Article
PubMed
TargetAromatase(Human)
University of Bari

LigandPNGBDBM9478(CHEMBL224649 | 7-(1H-Imidazol-1-ylmethyl)-2H-chrom...)
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 Article
PubMed
TargetAromatase(Human)
University of Bari

LigandPNGBDBM9473(CHEMBL225178 | 4-[2-(1H-Imidazol-1-yl)ethoxy]-2H-c...)
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 Article
PubMed
TargetAromatase(Human)
University of Bari

LigandPNGBDBM9486(6-(1H-imidazol-1-ylmethyl)-2H-chromene-2-thione | ...)
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
In DepthDetails Article
PubMed
TargetAromatase(Human)
University of Bari

LigandPNGBDBM9470(CHEMBL427247 | 4-(1H-Imidazol-1-ylmethyl)-2H-chrom...)
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 Article
PubMed
TargetAromatase(Human)
University of Bari

LigandPNGBDBM9469(CHEMBL387892 | 3-(1H-Imidazol-1-ylmethyl)-7-methox...)
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 Article
PubMed
TargetAromatase(Human)
University of Bari

LigandPNGBDBM9462(5-(1H-Imidazol-1-yl)-2-methyl-5H-indeno[1,2-d]pyri...)
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 Article
PubMed
TargetAromatase(Human)
University of Bari

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 Article
PubMed
TargetAromatase(Human)
University of Bari

LigandPNGBDBM9472(CHEMBL388604 | 7-Methoxy-4-(1H-1,2,4-triazol-1-ylm...)
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 Article
PubMed
TargetAromatase(Human)
University of Bari

LigandPNGBDBM9468(CHEMBL376371 | 1-(9-Phenyl-9H-fluoren-9-yl)-1H-1,2...)
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 Article
PubMed
TargetAromatase(Human)
University of Bari

LigandPNGBDBM9482(CHEMBL224786 | 4-(1H-Imidazol-1-ylmethyl)-3-phenyl...)
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 Article
PubMed
TargetAromatase(Human)
University of Bari

LigandPNGBDBM8935(CHEMBL448463 | dihydronaphthalene derivative | 5-[...)
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 Article
PubMed
TargetAromatase(Human)
University of Bari

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 Article
PubMed