Compile Data Set for Download or QSAR
Found 73 with Last Name = 'picot' and Initial = 'n'
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50047260(4,4'-((1H-imidazol-1-yl)methylene)dibenzonitrile |...)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50008733(1-(4-Cyanobenzyl)-1H-imidazole | 4-((1H-imidazol-1...)copy SMILEScopy InChI
Affinity DataIC50: 7nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM13061(4,4 -(1H-1,2,4-triazol-1-ylmethanediyl)dibenzonitr...)copy SMILEScopy InChI
Affinity DataIC50: 8nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMedDrugBank
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351827(CHEMBL224789)copy SMILEScopy InChI
Affinity DataIC50: 8nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50014788(1-Benzhydryl-1H-imidazole | CHEMBL336638)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351855(CHEMBL1824769)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351859(CHEMBL1825020)copy SMILEScopy InChI
Affinity DataIC50: 150nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM7887(1-Benzylimidazole (BI) | 1-benzyl-1H-imidazole | 1...)copy SMILEScopy InChI
Affinity DataIC50: 150nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetPolyunsaturated fatty acid 5-lipoxygenase(Homo sapiens (Human))
Université de Moncton

Curated by ChEMBL
LigandPNGBDBM50277011((2E,2'E)-(1,1'-(2,2-bis((4-(((E)-3-(3,4-dihydroxyp...)copy SMILEScopy InChI
Affinity DataIC50: 660nMAssay Description:Inhibition of human 5LOX expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21R6QCDPubMed
TargetPolyunsaturated fatty acid 5-lipoxygenase(Homo sapiens (Human))
Université de Moncton

Curated by ChEMBL
LigandPNGBDBM50276981((E)-2-(4-(cinnamoyloxymethyl)-1H-1,2,3-triazol-1-y...)copy SMILEScopy InChI
Affinity DataIC50: 680nMAssay Description:Inhibition of human 5LOX expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21R6QCDPubMed
TargetPolyunsaturated fatty acid 5-lipoxygenase(Homo sapiens (Human))
Université de Moncton

Curated by ChEMBL
LigandPNGBDBM50277009((E)-(1-(2-((E)-3-(3,4-dihydroxyphenyl)acryloyloxy)...)copy SMILEScopy InChI
Affinity DataIC50: 740nMAssay Description:Inhibition of human 5LOX expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21R6QCDPubMed
TargetPolyunsaturated fatty acid 5-lipoxygenase(Homo sapiens (Human))
Université de Moncton

Curated by ChEMBL
LigandPNGBDBM50277010((2E,2'E)-(1,1'-(2-((4-(((E)-3-(3,4-dihydroxyphenyl...)copy SMILEScopy InChI
Affinity DataIC50: 790nMAssay Description:Inhibition of human 5LOX expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21R6QCDPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351863(CHEMBL1825024)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+3nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351885(CHEMBL1825045)copy SMILEScopy InChI
Affinity DataIC50: 1.36E+3nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351887(CHEMBL1825047)copy SMILEScopy InChI
Affinity DataIC50: 2.27E+3nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351875(CHEMBL1825036)copy SMILEScopy InChI
Affinity DataIC50: 2.34E+3nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351886(CHEMBL1825046)copy SMILEScopy InChI
Affinity DataIC50: 2.78E+3nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351866(CHEMBL1825027)copy SMILEScopy InChI
Affinity DataIC50: 3.07E+3nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351869(CHEMBL1825030)copy SMILEScopy InChI
Affinity DataIC50: 3.38E+3nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351871(CHEMBL1825032)copy SMILEScopy InChI
Affinity DataIC50: 3.91E+3nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351860(CHEMBL1825021)copy SMILEScopy InChI
Affinity DataIC50: 4.11E+3nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351874(CHEMBL1825035)copy SMILEScopy InChI
Affinity DataIC50: 4.17E+3nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351864(CHEMBL1825025)copy SMILEScopy InChI
Affinity DataIC50: 4.37E+3nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351841(CHEMBL1824755)copy SMILEScopy InChI
Affinity DataIC50: 4.58E+3nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351836(CHEMBL1824750)copy SMILEScopy InChI
Affinity DataIC50: 4.64E+3nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351828(CHEMBL1824742)copy SMILEScopy InChI
Affinity DataIC50: 4.70E+3nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351884(CHEMBL1825044)copy SMILEScopy InChI
Affinity DataIC50: 5.04E+3nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351829(CHEMBL1824743)copy SMILEScopy InChI
Affinity DataIC50: 5.07E+3nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351865(CHEMBL1825026)copy SMILEScopy InChI
Affinity DataIC50: 5.26E+3nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351873(CHEMBL1825034)copy SMILEScopy InChI
Affinity DataIC50: 5.62E+3nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351870(CHEMBL1825031)copy SMILEScopy InChI
Affinity DataIC50: 6.09E+3nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351880(CHEMBL1825041)copy SMILEScopy InChI
Affinity DataIC50: 6.40E+3nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351878(CHEMBL1825039)copy SMILEScopy InChI
Affinity DataIC50: 7.47E+3nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351837(CHEMBL1824751)copy SMILEScopy InChI
Affinity DataIC50: 7.73E+3nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351867(CHEMBL1825028)copy SMILEScopy InChI
Affinity DataIC50: 7.88E+3nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351881(CHEMBL1825042)copy SMILEScopy InChI
Affinity DataIC50: 7.98E+3nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351872(CHEMBL1825033)copy SMILEScopy InChI
Affinity DataIC50: 9.16E+3nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351879(CHEMBL1825040)copy SMILEScopy InChI
Affinity DataIC50: 9.53E+3nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351882(CHEMBL1825043)copy SMILEScopy InChI
Affinity DataIC50: 9.77E+3nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351833(CHEMBL1824747)copy SMILEScopy InChI
Affinity DataIC50: 1.03E+4nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351830(CHEMBL1824744)copy SMILEScopy InChI
Affinity DataIC50: 1.06E+4nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351883(CHEMBL272339)copy SMILEScopy InChI
Affinity DataIC50: 1.06E+4nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351889(CHEMBL1825049)copy SMILEScopy InChI
Affinity DataIC50: 1.07E+4nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351868(CHEMBL1825029)copy SMILEScopy InChI
Affinity DataIC50: 1.07E+4nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351838(CHEMBL1824752)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+4nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351842(CHEMBL1824756)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+4nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351834(CHEMBL1824748)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+4nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351876(CHEMBL1825037)copy SMILEScopy InChI
Affinity DataIC50: 1.16E+4nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351851(CHEMBL1824765)copy SMILEScopy InChI
Affinity DataIC50: 1.16E+4nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
TargetAromatase(Homo sapiens (Human))
Universit£ de Moncton

Curated by ChEMBL
LigandPNGBDBM50351857(CHEMBL1825018)copy SMILEScopy InChI
Affinity DataIC50: 1.19E+4nMAssay Description:Inhibition of aromatase using 7-methoxy-4-trifluoromethyl coumarin as substrate after 30 mins by fluorescence-based colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24WTRPubMed
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