Compile Data Set for Download or QSAR
maximum 50k data
Found 49 Enz. Inhib. hit(s) with all data for entry = 50046643
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123025(CHEMBL3623231)
Affinity DataIC50:  0.100nMAssay Description:Inhibition of aromatase in human JEG-3 cells using [1beta-3H]androstenedione as substrate after 1 hr by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123026(CHEMBL3623232)
Affinity DataIC50:  0.200nMAssay Description:Inhibition of aromatase in human JEG-3 cells using [1beta-3H]androstenedione as substrate after 1 hr by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123026(CHEMBL3623232)
Affinity DataIC50:  2.5nMAssay Description:Inhibition of steroid sulfatase in human JEG-3 cells using [6,7-3H]E1S as substrate after 1 hr by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM24306(Letrozole derivative, 40 | {2-bromo-4-[(4-cyanophe...)
Affinity DataIC50:  3nMAssay Description:Inhibition of aromatase in human JEG-3 cells using [1beta-3H]androstenedione as substrate after 1 hr by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50398452(CHEMBL2179110)
Affinity DataIC50:  12nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50035204(4-(6-Methoxy-1a,2,3,7b-tetrahydro-1H-cyclopropa[a]...)
Affinity DataIC50:  30nMAssay Description:Inhibition of human placental aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50035204(4-(6-Methoxy-1a,2,3,7b-tetrahydro-1H-cyclopropa[a]...)
Affinity DataIC50:  30nMAssay Description:Inhibition of human placental aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50097366(4-((1H-imidazol-1-yl)methyl)-1-nitro-4aH-xanthen-9...)
Affinity DataIC50:  40nMAssay Description:Inhibition of human placental aromatase in presence of [1beta,2beta-3H] testosterone by Thompson and Siiteri methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50075009(1-Ethyl-5-[(4-fluoro-phenyl)-imidazol-1-yl-methyl]...)
Affinity DataIC50:  40nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123024(CHEMBL3623227)
Affinity DataIC50:  41nMAssay Description:Inhibition of human placental aromatase using [1,2,6,7-3H] androstenedione as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123152(CHEMBL3219600)
Affinity DataIC50:  41nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50097373(4-((1H-imidazol-1-yl)methyl)-9-oxo-9H-xanthene-1-c...)
Affinity DataIC50:  43nMAssay Description:Inhibition of human placental aromatase in presence of [1beta,2beta-3H] testosterone by Thompson and Siiteri methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM9475(4-(1H-Imidazol-1-ylmethyl)-7-phenoxy-2H-chromen-2-...)
Affinity DataIC50:  51nMAssay Description:Inhibition of human placental aromatase in presence of [1beta,2beta-3H] testosterone by Thompson and Siiteri methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123153(CHEMBL3623225)
Affinity DataIC50:  100nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123016(CHEMBL3623214)
Affinity DataIC50:  160nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Rattus norvegicus)
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50049763(2-[1-(3H-Imidazol-4-yl)-meth-(E)-ylidene]-3,4-dihy...)
Affinity DataIC50:  170nMAssay Description:Inhibition of rat ovarian aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123012(CHEMBL3623217)
Affinity DataIC50:  170nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123017(CHEMBL3623213)
Affinity DataIC50:  180nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123023(CHEMBL3623226)
Affinity DataIC50:  190nMAssay Description:Inhibition of human placental aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123019(CHEMBL3621226)
Affinity DataIC50:  220nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123020(CHEMBL3623209)
Affinity DataIC50:  250nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Rattus norvegicus)
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123022(CHEMBL169251)
Affinity DataIC50:  260nMAssay Description:Inhibition of rat ovarian aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123021(CHEMBL3623208)
Affinity DataIC50:  420nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123151(CHEMBL3623223)
Affinity DataIC50:  470nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123030(CHEMBL3623219)
Affinity DataIC50:  480nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM7461(5,7-dihydroxy-2-phenyl-4H-chromen-4-one | 5,7-dihy...)
Affinity DataIC50:  500nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM10027(5-[2-(1H-imidazol-1-yl)ethyl]-7,8-dihydroquinoline...)
Affinity DataIC50:  500nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123014(CHEMBL3623215)
Affinity DataIC50:  510nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123011(CHEMBL3623218)
Affinity DataIC50:  970nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123013(CHEMBL3623216)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM7458(5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one...)
Affinity DataIC50:  1.20E+3nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123027(CHEMBL3623212)
Affinity DataIC50:  2.40E+3nMAssay Description:Inhibition of human placental aromatase assessed as conversion of 3H2O from [1beta,2beta-3H] testosterone after 20 mins by scintillation spectrometer...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM24306(Letrozole derivative, 40 | {2-bromo-4-[(4-cyanophe...)
Affinity DataIC50:  2.60E+3nMAssay Description:Inhibition of steroid sulfatase in human JEG-3 cells using [6,7-3H]E1S as substrate after 1 hr by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123155(CHEMBL3623230)
Affinity DataIC50:  2.70E+3nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM13062((4-{[4-(sulfamoyloxy)phenyl](1H-1,2,4-triazol-1-yl...)
Affinity DataIC50:  3.00E+3nMAssay Description:Inhibition of aromatase in human JEG-3 cells using [1beta-3H]androstenedione as substrate after 1 hr by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123015(CHEMBL2282050)
Affinity DataIC50:  4.40E+3nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Rattus norvegicus)
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50009605(2-(pyridin-4-ylmethylene)-3,4-dihydronaphthalen-1(...)
Affinity DataIC50:  4.60E+3nMAssay Description:Inhibition of rat ovarian aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123018(CHEMBL2003274)
Affinity DataIC50:  5.20E+3nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123154(CHEMBL3623229)
Affinity DataIC50:  6.20E+3nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

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))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50028962(CHEMBL275638 | flavone)
Affinity DataIC50:  8.00E+3nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM13062((4-{[4-(sulfamoyloxy)phenyl](1H-1,2,4-triazol-1-yl...)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of steroid sulfatase in human JEG-3 cells using [6,7-3H]E1S as substrate after 1 hr by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM7460(2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-4H-chrome...)
Affinity DataIC50:  1.20E+4nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM92556(Neoflavonoid, 8)
Affinity DataIC50:  1.21E+4nMAssay Description:Inhibition of aromatase (unknown origin) after 30 mins by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123029(CHEMBL3623221)
Affinity DataIC50:  2.80E+4nMAssay Description:Inhibition of human placental aromatase assessed as conversion of 3H2O from [1beta-3H]AD after 20 mins by Siiteri and Thompson methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123028(CHEMBL3623220)
Affinity DataIC50:  3.10E+4nMAssay Description:Inhibition of human placental aromatase assessed as conversion of 3H2O from [1beta-3H]AD after 20 mins by Siiteri and Thompson methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123150(CHEMBL3623222)
Affinity DataIC50:  4.40E+4nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM9461(5,7-dihydroxy-3-(4-methoxyphenyl)-4H-chromen-4-one...)
Affinity DataIC50:  1.13E+5nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM9454(7-(benzyloxy)-3-phenyl-2-[(pyridin-4-ylmethyl)sulf...)
Affinity DataIC50:  2.10E+5nMAssay Description:Inhibition of human placental aromatase assessed as conversion of [1beta-3H]androst-4-ene-3,17-dione to estrone after 15 mins by scintillation counti...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed