Compile Data Set for Download or QSAR
Found 72 Enz. Inhib. hit(s) with all data for entry = 50009084
TargetEstrogen receptor(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50254908(4-[1-(4-hydroxyphenyl)-4-methyl-5-{4-[2-(piperidin...)copy SMILEScopy InChI
Affinity DataKi:  2.70nMAssay Description:Inhibition of ERalpha in human MCF7 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetAromatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50525255(CHEMBL3754505)copy SMILEScopy InChI
Affinity DataKi:  61nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetAromatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50525268(CHEMBL3753089)copy SMILEScopy InChI
Affinity DataKi:  174nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetAromatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM9454(7-(benzyloxy)-3-phenyl-2-[(pyridin-4-ylmethyl)sulf...)copy SMILEScopy InChI
Affinity DataKi:  220nMAssay Description:Inhibition of human placental microsome aromatase using [1beta[3H]]androst-4-ene-3,17-dione as substrate after 15 mins in presence of NADPH by liquid...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50525262(CHEMBL4444347)copy SMILEScopy InChI
Affinity DataKi:  350nMAssay Description:Inhibition of sulfatase (unknown origin) using [3H]E1S as substrate after 20 mins by scintillation counting methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50254908(4-[1-(4-hydroxyphenyl)-4-methyl-5-{4-[2-(piperidin...)copy SMILEScopy InChI
Affinity DataKi:  1.80E+3nMAssay Description:Inhibition of ERbeta in human MCF7 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetAromatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM9461(5,7-dihydroxy-3-(4-methoxyphenyl)-4H-chromen-4-one...)copy SMILEScopy InChI
Affinity DataKi:  1.20E+4nMAssay Description:Inhibition of human placental microsome aromatase using [1beta,2beta3H]androstenedione as substrate after 15 mins in presence of NADPH by liquid scin...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50370691(CHEMBL1628004)copy SMILEScopy InChI
Affinity DataKi:  2.80E+4nMAssay Description:Inhibition of sulfatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50073853(CHEMBL33862 | Sulfamic acid 4-{(E)-1-[4-(2-dimethy...)copy SMILEScopy InChI
Affinity DataKi:  3.59E+4nMAssay Description:Inhibition of sulfatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50073852(CHEMBL32172 | Sulfamic acid 4-{(Z)-1-[4-(2-dimethy...)copy SMILEScopy InChI
Affinity DataKi: >5.00E+5nMAssay Description:Inhibition of sulfatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetEstrogen receptor(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50525253(CHEMBL4518283)copy SMILEScopy InChI
Affinity DataIC50: 0.0400nMAssay Description:Inhibition of ERalpha in human MCF7 cells after 36 hrs by Western blot analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50118551(CHEMBL137392 | Sulfamic acid 2-tert-butyl-4-oxo-4H...)copy SMILEScopy InChI
Affinity DataIC50: 0.0470nMAssay Description:Inhibition of human sulfatase using 4-methylumbelliferyl sulfate as substrate after 60 minsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50118567(CHEMBL137692 | Sulfamic acid 2-nonyl-4-oxo-4H-chro...)copy SMILEScopy InChI
Affinity DataIC50: 0.0890nMAssay Description:Inhibition of human sulfatase using 4-methylumbelliferyl sulfate as substrate after 60 minsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetAromatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50525257(CHEMBL4520995)copy SMILEScopy InChI
Affinity DataIC50: 0.120nMAssay Description:Inhibition of human placental microsome aromatase using [1beta,2beta3H]androstenedione as substrate by liquid scintillation counting methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50369432(CHEMBL1627465)copy SMILEScopy InChI
Affinity DataIC50: 0.150nMAssay Description:Inhibition of sulfatase (unknown origin) using [3H]E1S as substrate after 18 hrsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetAromatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50525260(CHEMBL4465348)copy SMILEScopy InChI
Affinity DataIC50: 0.200nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetAromatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50121079(CHEMBL3622064)copy SMILEScopy InChI
Affinity DataIC50: 0.25nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetAromatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50121105(CHEMBL3622055)copy SMILEScopy InChI
Affinity DataIC50: 0.260nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50118560(CHEMBL262050 | Sulfamic acid 2-adamantan-1-yl-4-ox...)copy SMILEScopy InChI
Affinity DataIC50: 0.340nMAssay Description:Inhibition of sulfatase (unknown origin) using 4-MUS as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50369431(CHEMBL1627878)copy SMILEScopy InChI
Affinity DataIC50: 0.390nMAssay Description:Inhibition of sulfatase (unknown origin) using [3H]E1S as substrate after 18 hrsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetAromatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM10016(4-{[(4-bromophenyl)methyl](4H-1,2,4-triazol-4-yl)a...)copy SMILEScopy InChI
Affinity DataIC50: 0.400nMAssay Description:Inhibition of human placental microsome aromatase using [1beta,2beta3H]androstenedione as substrate by liquid scintillation counting methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetAromatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50047259(4-(1-(1H-imidazol-1-yl)vinyl)benzonitrile | 4-(1-I...)copy SMILEScopy InChI
Affinity DataIC50: 0.700nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetAromatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM10020((2-bromo-4-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-yl...)copy SMILEScopy InChI
Affinity DataIC50: 0.820nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50369432(CHEMBL1627465)copy SMILEScopy InChI
Affinity DataIC50: 1.40nMAssay Description:Inhibition of sulfatase (unknown origin) using [3H]DHEAS as substrate after 18 hrsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetAromatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50121078(CHEMBL3622063)copy SMILEScopy InChI
Affinity DataIC50: 2.10nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetAromatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM10019((2-chloro-4-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-y...)copy SMILEScopy InChI
Affinity DataIC50: 2.30nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50525260(CHEMBL4465348)copy SMILEScopy InChI
Affinity DataIC50: 2.5nMAssay Description:Inhibition of sulfatase (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetEstrogen receptor(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50041611((2E)-3-{4-[(1E)-1,2-DIPHENYLBUT-1-ENYL]PHENYL}ACRY...)copy SMILEScopy InChI
Affinity DataIC50: 2.60nMAssay Description:Inhibition of Fluormone-ES2 binding affinity to ERalpha (unknown origin) after 2 hrs by fluorescent polarization based competition binding assayMore data for this Ligand-Target Pair
TargetSteryl-sulfatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50121196(CHEMBL3622029)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibition of sulfatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetEstrogen receptor(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50525263(CHEMBL4444074)copy SMILEScopy InChI
Affinity DataIC50: 3.5nMAssay Description:Inhibition of ERalpha (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50369431(CHEMBL1627878)copy SMILEScopy InChI
Affinity DataIC50: 4.10nMAssay Description:Inhibition of sulfatase (unknown origin) using [3H]DHEAS as substrate after 18 hrsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50525261(CHEMBL4436482)copy SMILEScopy InChI
Affinity DataIC50: 14nMAssay Description:Inhibition of sulfatase (unknown origin) expressed in HEK293 cells using [3H]DHEAS as substrate after 2 hrs by liquid scintillation counting methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM10019((2-chloro-4-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-y...)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:Inhibition of sulfatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50363594(CHEMBL1627429)copy SMILEScopy InChI
Affinity DataIC50: 24nMAssay Description:Inhibition of sulfatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50121078(CHEMBL3622063)copy SMILEScopy InChI
Affinity DataIC50: 26nMAssay Description:Inhibition of sulfatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50366532(CHEMBL518966)copy SMILEScopy InChI
Affinity DataIC50: 28nMAssay Description:Inhibition of sulfatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50121058(CHEMBL275331)copy SMILEScopy InChI
Affinity DataIC50: 30nMAssay Description:Inhibition of human sulfatase using 4-methylumbelliferyl sulfate as substrate after 60 minsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetEstrogen receptor(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50525266(CHEMBL4547986)copy SMILEScopy InChI
Affinity DataIC50: 30nMAssay Description:Inhibition of ERalpha (unknown origin) after 18 hrs by dual luciferase reporter gene assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM10020((2-bromo-4-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-yl...)copy SMILEScopy InChI
Affinity DataIC50: 39nMAssay Description:Inhibition of sulfatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetAromatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50097366(4-((1H-imidazol-1-yl)methyl)-1-nitro-4aH-xanthen-9...)copy SMILEScopy InChI
Affinity DataIC50: 40nMAssay Description:Inhibition of human aromatase using [1beta,2beta3H]-]testosterone as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetAromatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50525256(CHEMBL4540847)copy SMILEScopy InChI
Affinity DataIC50: 41nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetEstrogen receptor(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50084948(CHEMBL195515 | GW7604)copy SMILEScopy InChI
Affinity DataIC50: 43nMAssay Description:Inhibition of Fluormone-ES2 binding affinity to ERalpha (unknown origin) after 2 hrs by fluorescent polarization based competition binding assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetAromatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50097373(4-((1H-imidazol-1-yl)methyl)-9-oxo-9H-xanthene-1-c...)copy SMILEScopy InChI
Affinity DataIC50: 43nMAssay Description:Inhibition of human aromatase using [1beta,2beta3H]-]testosterone as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50525261(CHEMBL4436482)copy SMILEScopy InChI
Affinity DataIC50: 46nMAssay Description:Inhibition of sulfatase (unknown origin) expressed in HEK293 cells using [3H]E1S as substrate after 2 hrs by liquid scintillation counting methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50525258(CHEMBL4529949)copy SMILEScopy InChI
Affinity DataIC50: 56nMAssay Description:Inhibition of sulfatase (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50525270(CHEMBL4435618)copy SMILEScopy InChI
Affinity DataIC50: 72nMAssay Description:Inhibition of human placental microsome sulfatase using estrone sulfate as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetEstrogen receptor(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50525254(CHEMBL4475271)copy SMILEScopy InChI
Affinity DataIC50: 80nMAssay Description:Inhibition of Estrogen receptor (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetAromatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50525267(CHEMBL4583456)copy SMILEScopy InChI
Affinity DataIC50: 91nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetReceptor tyrosine-protein kinase erbB-2(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50525254(CHEMBL4475271)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Inhibition of HER2 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
TargetAromatase(Homo sapiens (Human))
Indian Institute of Technology (BHU)

Curated by ChEMBL
LigandPNGBDBM50525252(CHEMBL1997442)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Inhibition of human placental microsome aromatase using [1beta,2beta3H]androstenedione as substrate after 15 mins in presence of NADPH by liquid scin...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W099B9PubMed
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