BDBM50152627 2-(4-HYDROXY-PHENYL)BENZOFURAN-5-OL::2-(4-Hydroxy-phenyl)-benzofuran-5-ol::CHEMBL367588

SMILES Oc1ccc(cc1)-c1cc2cc(O)ccc2o1

InChI Key InChIKey=SNNNDCMXZYWCCI-UHFFFAOYSA-N

Data  4 IC50  1 EC50

PDB links: 1 PDB ID matches this monomer.

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50152627   

TargetEstrogen receptor(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50152627(2-(4-HYDROXY-PHENYL)BENZOFURAN-5-OL | 2-(4-Hydroxy...)
Affinity DataIC50:  176nMAssay Description:Binding affinity for human Estrogen receptor alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50152627(2-(4-HYDROXY-PHENYL)BENZOFURAN-5-OL | 2-(4-Hydroxy...)
Affinity DataIC50:  6nMAssay Description:Binding affinity for human Estrogen receptor betaMore data for this Ligand-Target Pair
TargetEstrogen receptor beta(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50152627(2-(4-HYDROXY-PHENYL)BENZOFURAN-5-OL | 2-(4-Hydroxy...)
Affinity DataEC50:  5.70nMAssay Description:Displacement of [3H]-17beta-E2 from human ERbeta LBD by solid phase competitive radio ligand binding assayMore data for this Ligand-Target Pair
TargetEstrogen receptor beta(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50152627(2-(4-HYDROXY-PHENYL)BENZOFURAN-5-OL | 2-(4-Hydroxy...)
Affinity DataIC50:  6nMAssay Description:Inhibitory concentration against human ER beta expressed in Escherichia coli was determined using [3H]17-beta-estradiol as radio ligandMore data for this Ligand-Target Pair
TargetEstrogen receptor(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50152627(2-(4-HYDROXY-PHENYL)BENZOFURAN-5-OL | 2-(4-Hydroxy...)
Affinity DataIC50:  176nMAssay Description:Inhibitory concentration against human ER alpha expressed in Escherichia coli was determined using [3H]17-beta-estradiol as radio ligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed