Compile Data Set for Download or QSAR
Found 21 Enz. Inhib. hit(s) with all data for entry = 50047641
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50180683(CHEMBL3818720)copy SMILEScopy InChI
Affinity DataKi:  84nMAssay Description:Competitive inhibition of human placental microsomal aromatase using androgen as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7D2SPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)copy SMILEScopy InChI
Affinity DataIC50: 0.00400nMAssay Description:Inhibition of aromatase (unknown origin) transfected in human MCF7 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7D2SPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50123026(CHEMBL3623232)copy SMILEScopy InChI
Affinity DataIC50: 0.200nMAssay Description:Inhibition of aromatase in human JEG3 cells using [1beta-3H] androstenedione as substrate assessed as tritiated H2O release after 1 hr by scintillati...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7D2SPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50180685(CHEMBL3818343)copy SMILEScopy InChI
Affinity DataIC50: 0.900nMAssay Description:Inhibition of aromatase in human JEG3 cells using [1beta-3H] androstenedione as substrate assessed as tritiated H2O release after 1 hr by scintillati...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7D2SPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50014315((rac)-6-((4-chlorophenyl)(1H-1,2,4-triazol-1-yl)me...)copy SMILEScopy InChI
Affinity DataIC50: 1.40nMAssay Description:Reversible inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7D2SPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM10015(2-[3-(1-cyano-1-methylethyl)-5-(1H-1,2,4-triazol-1...)copy SMILEScopy InChI
Affinity DataIC50: 3.60nMAssay Description:Inhibition of aromatase (unknown origin) transfected in human MCF7 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7D2SPubMedDrugBank
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50435004(CHEMBL2386284)copy SMILEScopy InChI
Affinity DataIC50: 30nMAssay Description:Inhibition of human placental microsomal aromatase using testosterone as substrate assessed as formation of estradiol after 10 minsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7D2SPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50240798((8R,9S,10R,13S,14S)-4-Hydroxy-10,13-dimethyl-1,6,7...)copy SMILEScopy InChI
Affinity DataIC50: 30nMAssay Description:Inhibition of particulate fractions of human breast cancer derived aromataseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7D2SPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50180688(CHEMBL3818725)copy SMILEScopy InChI
Affinity DataIC50: 168nMAssay Description:Inhibition of human placental microsomal aromatase using [1beta-3H] androstenedione as substrate assessed as tritiated H2O release preincubated for 5...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7D2SPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50123012(CHEMBL3623217)copy SMILEScopy InChI
Affinity DataIC50: 169nMAssay Description:Inhibition of human placental microsomal aromatase using [1beta-3H] androstenedione as substrate assessed as tritiated H2O release after 5 mins by be...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7D2SPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50180689(CHEMBL3819184)copy SMILEScopy InChI
Affinity DataIC50: 180nMAssay Description:Inhibition of human placental microsomal aromatase using [1beta-3H] androstenedione as substrate assessed as tritiated H2O release preincubated for 5...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7D2SPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50180690(CHEMBL3819549)copy SMILEScopy InChI
Affinity DataIC50: 450nMAssay Description:Inhibition of human placental microsomal aromatase using [1beta-3H] androstenedione as substrate assessed as tritiated H2O release after 15 mins by l...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7D2SPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50123151(CHEMBL3623223)copy SMILEScopy InChI
Affinity DataIC50: 470nMAssay Description:Inhibition of human placental microsomal aromatase using [1beta-3H] androstenedione as substrate assessed as tritiated H2O release after 15 mins by l...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7D2SPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50180687(CHEMBL3818442)copy SMILEScopy InChI
Affinity DataIC50: 512nMAssay Description:Inhibition of human placental microsomal aromatase using [1beta-3H] androstenedione as substrate assessed as tritiated H2O release preincubated for 5...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7D2SPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50180692(CHEMBL3818728)copy SMILEScopy InChI
Affinity DataIC50: 590nMAssay Description:Inhibition of human placental microsomal aromatase using [1beta-3H] androstenedione as substrate assessed as tritiated H2O release after 15 mins by l...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7D2SPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50180691(CHEMBL3818338)copy SMILEScopy InChI
Affinity DataIC50: 750nMAssay Description:Inhibition of human placental microsomal aromatase using [1beta-3H] androstenedione as substrate assessed as tritiated H2O release after 15 mins by l...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7D2SPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50180686(CHEMBL3818279)copy SMILEScopy InChI
Affinity DataIC50: 800nMAssay Description:Inhibition of human aromatase using testosterone as substrate incubated for 1 hr by HTRF assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7D2SPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50123013(CHEMBL3623216)copy SMILEScopy InChI
Affinity DataIC50: 1.02E+3nMAssay Description:Inhibition of human placental microsomal aromatase using [1beta-3H] androstenedione as substrate assessed as tritiated H2O release preincubated for 5...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7D2SPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50435003(ENDOXIFEN)copy SMILEScopy InChI
Affinity DataIC50: 6.00E+3nMAssay Description:Inhibition of human placental microsomal aromatase using testosterone as substrate assessed as formation of estradiol after 10 minsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7D2SPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM9460(3-(4-aminophenyl)-3-ethyl-piperidine-2,6-dione | 3...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human aromatase transfected in human MCF7 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7D2SPubMedDrugBank
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50180684(4-OHT | Afimoxifene | TamoGel)copy SMILEScopy InChI
Affinity DataIC50: 5.30E+5nMAssay Description:Inhibition of human placental microsomal aromatase using testosterone as substrate assessed as formation of estradiol after 10 minsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7D2SPubMed