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Found 39 with Last Name = 'bankemper' and Initial = 't'
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM13061(4,4 -(1H-1,2,4-triazol-1-ylmethanediyl)dibenzonitr...)
Affinity DataIC50:  2.80nMAssay Description:Inhibition of human recombinant aromatase expressed in baculovirus-infected cell system using 7-methoxy-trifluoromethylcoumarin as substrate after 30...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM10015(2-[3-(1-cyano-1-methylethyl)-5-(1H-1,2,4-triazol-1...)
Affinity DataIC50:  12nMAssay Description:Inhibition of aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50380169(CHEMBL2011180)
Affinity DataIC50:  260nMAssay Description:Inhibition of human recombinant aromatase expressed in baculovirus/insect cells using 7-methoxy-trifluoromethylcoumarin as substrate after 30 mins by...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50445501(CHEMBL3105528)
Affinity DataIC50:  800nMAssay Description:Inhibition of human recombinant aromatase expressed in baculovirus-infected cell system using 7-methoxy-trifluoromethylcoumarin as substrate after 30...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM31768(CHEMBL295698 | Ketoconazole | Nizoral | Panfungol)
Affinity DataIC50:  1.30E+3nMAssay Description:Inhibition of human recombinant aromatase expressed in baculovirus/insect cells using 7-methoxy-trifluoromethylcoumarin as substrate after 30 mins by...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM7461(5,7-dihydroxy-2-phenyl-4H-chromen-4-one | 5,7-dihy...)
Affinity DataIC50:  1.50E+3nMAssay Description:Inhibition of aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50380168(CHEMBL2011177)
Affinity DataIC50:  2.40E+3nMAssay Description:Inhibition of human recombinant aromatase expressed in baculovirus/insect cells using 7-methoxy-trifluoromethylcoumarin as substrate after 30 mins by...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50445503(CHEMBL3105526)
Affinity DataIC50:  2.50E+3nMAssay Description:Inhibition of human recombinant aromatase expressed in baculovirus-infected cell system using 7-methoxy-trifluoromethylcoumarin as substrate after 30...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50380176(CHEMBL2011188)
Affinity DataIC50:  5.10E+3nMAssay Description:Inhibition of human recombinant aromatase expressed in baculovirus/insect cells using 7-methoxy-trifluoromethylcoumarin as substrate after 30 mins by...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50380174(CHEMBL2011186)
Affinity DataIC50:  5.80E+3nMAssay Description:Inhibition of human recombinant aromatase expressed in baculovirus/insect cells using 7-methoxy-trifluoromethylcoumarin as substrate after 30 mins by...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50051358(2,3-Dihydroflavone | 2,3-dihydro-2-phenyl-4H-1-ben...)
Affinity DataIC50:  8.00E+3nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50028962(CHEMBL275638 | flavone)
Affinity DataIC50:  1.00E+4nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50380160(CHEMBL2011184)
Affinity DataIC50:  1.10E+4nMAssay Description:Inhibition of human recombinant aromatase expressed in baculovirus/insect cells using 7-methoxy-trifluoromethylcoumarin as substrate after 30 mins by...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50445509(CHEMBL3105517)
Affinity DataIC50:  1.50E+4nMAssay Description:Inhibition of human recombinant aromatase expressed in baculovirus-infected cell system using 7-methoxy-trifluoromethylcoumarin as substrate after 30...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50380168(CHEMBL2011177)
Affinity DataIC50:  1.70E+4nMAssay Description:Inhibition of aromatase in human MCF7 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50380164(CHEMBL2011173)
Affinity DataIC50:  1.80E+4nMAssay Description:Inhibition of human recombinant aromatase expressed in baculovirus/insect cells using 7-methoxy-trifluoromethylcoumarin as substrate after 30 mins by...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50445505(CHEMBL3105522)
Affinity DataIC50:  2.00E+4nMAssay Description:Inhibition of human recombinant aromatase expressed in baculovirus-infected cell system using 7-methoxy-trifluoromethylcoumarin as substrate after 30...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50380165(CHEMBL2011174)
Affinity DataIC50:  2.00E+4nMAssay Description:Inhibition of human recombinant aromatase expressed in baculovirus/insect cells using 7-methoxy-trifluoromethylcoumarin as substrate after 30 mins by...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50380167(CHEMBL2011176)
Affinity DataIC50:  2.00E+4nMAssay Description:Inhibition of human recombinant aromatase expressed in baculovirus/insect cells using 7-methoxy-trifluoromethylcoumarin as substrate after 30 mins by...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50380172(CHEMBL2011183)
Affinity DataIC50:  2.40E+4nMAssay Description:Inhibition of human recombinant aromatase expressed in baculovirus/insect cells using 7-methoxy-trifluoromethylcoumarin as substrate after 30 mins by...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50445508(CHEMBL3105519)
Affinity DataIC50:  2.40E+4nMAssay Description:Inhibition of human recombinant aromatase expressed in baculovirus-infected cell system using 7-methoxy-trifluoromethylcoumarin as substrate after 30...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50380162(CHEMBL2011171)
Affinity DataIC50:  2.90E+4nMAssay Description:Inhibition of human recombinant aromatase expressed in baculovirus/insect cells using 7-methoxy-trifluoromethylcoumarin as substrate after 30 mins by...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50380177(CHEMBL2011189)
Affinity DataIC50:  2.90E+4nMAssay Description:Inhibition of human recombinant aromatase expressed in baculovirus/insect cells using 7-methoxy-trifluoromethylcoumarin as substrate after 30 mins by...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50380173(CHEMBL2011185)
Affinity DataIC50:  3.00E+4nMAssay Description:Inhibition of human recombinant aromatase expressed in baculovirus/insect cells using 7-methoxy-trifluoromethylcoumarin as substrate after 30 mins by...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50380175(CHEMBL2011187)
Affinity DataIC50:  3.20E+4nMAssay Description:Inhibition of human recombinant aromatase expressed in baculovirus/insect cells using 7-methoxy-trifluoromethylcoumarin as substrate after 30 mins by...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50445506(CHEMBL3105521)
Affinity DataIC50:  3.30E+4nMAssay Description:Inhibition of human recombinant aromatase expressed in baculovirus-infected cell system using 7-methoxy-trifluoromethylcoumarin as substrate after 30...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50445507(CHEMBL3105520)
Affinity DataIC50:  3.50E+4nMAssay Description:Inhibition of human recombinant aromatase expressed in baculovirus-infected cell system using 7-methoxy-trifluoromethylcoumarin as substrate after 30...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50380179(CHEMBL1165711)
Affinity DataIC50:  4.10E+4nMAssay Description:Inhibition of human recombinant aromatase expressed in baculovirus/insect cells using 7-methoxy-trifluoromethylcoumarin as substrate after 30 mins by...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50380166(CHEMBL2011175)
Affinity DataIC50:  4.10E+4nMAssay Description:Inhibition of human recombinant aromatase expressed in baculovirus/insect cells using 7-methoxy-trifluoromethylcoumarin as substrate after 30 mins by...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50380163(CHEMBL2011172)
Affinity DataIC50:  4.40E+4nMAssay Description:Inhibition of human recombinant aromatase expressed in baculovirus/insect cells using 7-methoxy-trifluoromethylcoumarin as substrate after 30 mins by...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50380174(CHEMBL2011186)
Affinity DataIC50:  4.40E+4nMAssay Description:Inhibition of aromatase in human MCF7 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50380178(CHEMBL2011190)
Affinity DataIC50:  6.10E+4nMAssay Description:Inhibition of human recombinant aromatase expressed in baculovirus/insect cells using 7-methoxy-trifluoromethylcoumarin as substrate after 30 mins by...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50445502(CHEMBL3105527)
Affinity DataIC50:  6.71E+4nMAssay Description:Inhibition of human recombinant aromatase expressed in baculovirus-infected cell system using 7-methoxy-trifluoromethylcoumarin as substrate after 30...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50380170(CHEMBL2011181)
Affinity DataIC50:  9.70E+4nMAssay Description:Inhibition of human recombinant aromatase expressed in baculovirus/insect cells using 7-methoxy-trifluoromethylcoumarin as substrate after 30 mins by...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50380171(CHEMBL2011182)
Affinity DataIC50:  9.90E+4nMAssay Description:Inhibition of human recombinant aromatase expressed in baculovirus/insect cells using 7-methoxy-trifluoromethylcoumarin as substrate after 30 mins by...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM9461(5,7-dihydroxy-3-(4-methoxyphenyl)-4H-chromen-4-one...)
Affinity DataIC50:  1.13E+5nMAssay Description:Inhibition of aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50380180(CHEMBL2011192)
Affinity DataIC50:  1.60E+5nMAssay Description:Inhibition of aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50380161(CHEMBL2011191)
Affinity DataIC50:  1.70E+5nMAssay Description:Inhibition of aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Northern Kentucky University

Curated by ChEMBL
LigandPNGBDBM50445504(CHEMBL3105524)
Affinity DataIC50:  1.90E+5nMAssay Description:Inhibition of human recombinant aromatase expressed in baculovirus-infected cell system using 7-methoxy-trifluoromethylcoumarin as substrate after 30...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed