Compile Data Set for Download or QSAR
Found 2838 of ic50 data for polymerid = 1024,50000929
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
LigandPNGBDBM50539776(CHEMBL4639677)copy SMILEScopy InChI
Affinity DataIC50: 0.0100nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q251437DPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50539777(CHEMBL4632445)copy SMILEScopy InChI
Affinity DataIC50: 0.0100nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q251437DPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50337121(2-chloro-4-(((6-cyanobiphenyl-3-yl)(4H-1,2,4-triaz...)copy SMILEScopy InChI
Affinity DataIC50: 0.0150nMAssay Description:Inhibition of aromatase in human JEG-3 cells using [1beta-3H]androstenedione after 1 hr by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X067BNPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50337123(4-(((6-cyano-4'-methoxybiphenyl-3-yl)(4H-1,2,4-tri...)copy SMILEScopy InChI
Affinity DataIC50: 0.0150nMAssay Description:Inhibition of aromatase in human JEG-3 cells using [1beta-3H]androstenedione after 1 hr by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X067BNPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50337122(2-bromo-4-(((6-cyanobiphenyl-3-yl)(4H-1,2,4-triazo...)copy SMILEScopy InChI
Affinity DataIC50: 0.0180nMAssay Description:Inhibition of aromatase in human JEG-3 cells using [1beta-3H]androstenedione after 1 hr by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X067BNPubMed
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: 0.0300nMAssay Description:Aromatase inhibitor potency as iron-binding-related type II difference spectrumMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2SB46BPPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50337118(5'-((4-bromobenzyl)(4H-1,2,4-triazol-4-yl)amino)-2...)copy SMILEScopy InChI
Affinity DataIC50: 0.0500nMAssay Description:Inhibition of aromatase in human JEG-3 cells using [1beta-3H]androstenedione after 1 hr by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X067BNPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50592781(CHEMBL5203413)copy SMILES
Affinity DataIC50: 0.0900nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q251437DPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50337117(5'-(benzyl(4H-1,2,4-triazol-4-yl)amino)-2'-cyanobi...)copy SMILEScopy InChI
Affinity DataIC50: 0.100nMAssay Description:Inhibition of aromatase in human JEG-3 cells using [1beta-3H]androstenedione after 1 hr by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X067BNPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50307918(2-(5-((1H-1,2,4-triazol-1-yl)methyl)-3'-chloro-4'-...)copy SMILEScopy InChI
Affinity DataIC50: 0.100nMAssay Description:Inhibition of aromatse in human JEG3 cells by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959JGFPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50123025(CHEMBL3623231)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2ZC84Q6PubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM10007(4-[(6-methoxy-1-benzofuran-2-yl)(1H-1,2,4-triazol-...)copy SMILEScopy InChI
Affinity DataIC50: 0.110nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q251437DPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM10016(4-{[(4-bromophenyl)methyl](4H-1,2,4-triazol-4-yl)a...)copy SMILEScopy InChI
Affinity DataIC50: 0.120nMAssay Description:Inhibition of aromatase in human placental microsomeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2474CP9PubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

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
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50307884(3-CHLORO-2'-CYANO-5'-(1H-1,2,4-TRIAZOL-1-YLMETHYL)...)copy SMILEScopy InChI
Affinity DataIC50: 0.120nMAssay Description:Inhibition of aromatase (unknown origin) expressed in JEG-3 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2474CP9PubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM10004(1-[(4-fluorophenyl)(6-methoxy-1-benzofuran-2-yl)me...)copy SMILEScopy InChI
Affinity DataIC50: 0.150nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q251437DPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50307901(5-((1H-1,2,4-triazol-1-yl)methyl)-3'-chloro-4'-hyd...)copy SMILEScopy InChI
Affinity DataIC50: 0.150nMAssay Description:Inhibition of aromatase (unknown origin) expressed in JEG-3 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2474CP9PubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50337120(4-(((6-cyanobiphenyl-3-yl)(4H-1,2,4-triazol-4-yl)a...)copy SMILEScopy InChI
Affinity DataIC50: 0.150nMAssay Description:Inhibition of aromatase in human JEG-3 cells using [1beta-3H]androstenedione after 1 hr by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X067BNPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50307901(5-((1H-1,2,4-triazol-1-yl)methyl)-3'-chloro-4'-hyd...)copy SMILEScopy InChI
Affinity DataIC50: 0.150nMAssay Description:Inhibition of aromatse in human JEG3 cells by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959JGFPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM24341(4-{[(4-chloro-3-hydroxyphenyl)methyl](4H-1,2,4-tri...)copy SMILEScopy InChI
Affinity DataIC50: 0.180nMpH: 7.5 T: 2°CAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348HP4PubMed
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
LigandPNGBDBM50123026(CHEMBL3623232)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2ZC84Q6PubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

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))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50307900(5-((1H-1,2,4-triazol-1-yl)methyl)-4'-hydroxybiphen...)copy SMILEScopy InChI
Affinity DataIC50: 0.200nMAssay Description:Inhibition of aromatse in human JEG3 cells by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959JGFPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50307899(5-((1H-1,2,4-triazol-1-yl)methyl)biphenyl-2-carbon...)copy SMILEScopy InChI
Affinity DataIC50: 0.200nMAssay Description:Inhibition of aromatse in human JEG3 cells by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959JGFPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50337119(4-(((6-cyanobiphenyl-3-yl)(4H-1,2,4-triazol-4-yl)a...)copy SMILEScopy InChI
Affinity DataIC50: 0.210nMAssay Description:Inhibition of aromatase in human JEG-3 cells using [1beta-3H]androstenedione after 1 hr by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X067BNPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50307902(5-((1H-1,2,4-triazol-1-yl)methyl)-4'-chloro-3'-hyd...)copy SMILEScopy InChI
Affinity DataIC50: 0.220nMAssay Description:Inhibition of aromatse in human JEG3 cells by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959JGFPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50307919(5-((1H-1,2,4-triazol-1-yl)methyl)-3'-chlorobipheny...)copy SMILEScopy InChI
Affinity DataIC50: 0.220nMAssay Description:Inhibition of aromatse in human JEG3 cells by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959JGFPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

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))
State University of New York Upstate Medical University

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/Q2B27ZQ2PubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50121079(CHEMBL3622064)copy SMILEScopy InChI
Affinity DataIC50: 0.25nMAssay Description:Inhibition of aromatase (unknown origin) expressed in JEG-3 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2474CP9PubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50121105(CHEMBL3622055)copy SMILEScopy InChI
Affinity DataIC50: 0.260nMAssay Description:Inhibition of aromatase (unknown origin) expressed in JEG-3 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2474CP9PubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

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
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50121095(CHEMBL3622054)copy SMILEScopy InChI
Affinity DataIC50: 0.280nMAssay Description:Inhibition of aromatase (unknown origin) expressed in JEG-3 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2474CP9PubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50307881(3'-((1H-1,2,4-triazol-1-yl)methyl)-3-chloro-5'-(2-...)copy SMILEScopy InChI
Affinity DataIC50: 0.300nMAssay Description:Inhibition of aromatse in human JEG3 cells by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959JGFPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM24328(4-{[(4-hydroxy-3-iodophenyl)methyl](4H-1,2,4-triaz...)copy SMILEScopy InChI
Affinity DataIC50: 0.330nMpH: 7.5 T: 2°CAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348HP4PubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50307882(5'-((1H-1,2,4-triazol-1-yl)methyl)-4-chloro-2'-cya...)copy SMILEScopy InChI
Affinity DataIC50: 0.350nMAssay Description:Inhibition of aromatse in human JEG3 cells by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959JGFPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50592778(CHEMBL5175340)copy SMILES
Affinity DataIC50: 0.390nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q251437DPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

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))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50608157(CHEMBL5271052)copy SMILES
Affinity DataIC50: 0.400nMMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM24344(4-({[3-hydroxy-4-(trifluoromethyl)phenyl]methyl}(4...)copy SMILEScopy InChI
Affinity DataIC50: 0.400nMAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348HP4PubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50121073(CHEMBL3622056)copy SMILEScopy InChI
Affinity DataIC50: 0.420nMAssay Description:Inhibition of aromatase (unknown origin) expressed in JEG-3 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2474CP9PubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50460601(CHEMBL4227385)copy SMILEScopy InChI
Affinity DataIC50: 0.420nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20867Z3PubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50121074(CHEMBL3622057)copy SMILEScopy InChI
Affinity DataIC50: 0.450nMAssay Description:Inhibition of aromatase (unknown origin) expressed in JEG-3 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2474CP9PubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50592775(CHEMBL5184004)copy SMILES
Affinity DataIC50: 0.460nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q251437DPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM10001((4-chlorophenyl)(6-methoxy-1-benzofuran-2-yl)pyrid...)copy SMILEScopy InChI
Affinity DataIC50: 0.460nMMore data for this Ligand-Target Pair
In DepthDetails
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50337124(4-(((6-cyano-4'-fluorobiphenyl-3-yl)(4H-1,2,4-tria...)copy SMILEScopy InChI
Affinity DataIC50: 0.470nMAssay Description:Inhibition of aromatase in human JEG-3 cells using [1beta-3H]androstenedione after 1 hr by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X067BNPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM10005(1-[(4-chlorophenyl)(6-methoxy-1-benzofuran-2-yl)me...)copy SMILEScopy InChI
Affinity DataIC50: 0.470nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q251437DPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50307884(3-CHLORO-2'-CYANO-5'-(1H-1,2,4-TRIAZOL-1-YLMETHYL)...)copy SMILEScopy InChI
Affinity DataIC50: 0.5nMAssay Description:Inhibition of aromatse in human JEG3 cells by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959JGFPubMed
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