BDBM50458901 CHEMBL4210242

SMILES Oc1ccc(cc1)C1=C(C2OC1CC2S(=O)(=O)Oc1ccc(cc1)-c1ccccc1)c1ccc(\C=C\c2cc(O)cc(O)c2)cc1

InChI Key

Data  2 KI  2 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50458901   

TargetEstrogen receptor(Human)
Wuhan University

Curated by ChEMBL
LigandPNGBDBM50458901(CHEMBL4210242)
Affinity DataEC50:  4.93E+3nMAssay Description:Agonist activity at human ERalpha expressed in HEK293T cells after 24 hrs by ERE-based dual luciferase reporter gene assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/16/2020
Entry Details Article
PubMed
TargetEstrogen receptor beta(Human)
Wuhan University

Curated by ChEMBL
LigandPNGBDBM50458901(CHEMBL4210242)
Affinity DataEC50:  43nMAssay Description:Agonist activity at human ERbeta expressed in HEK293T cells after 24 hrs by ERE-based dual luciferase reporter gene assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/16/2020
Entry Details Article
PubMed
TargetEstrogen receptor(Human)
Wuhan University

Curated by ChEMBL
LigandPNGBDBM50458901(CHEMBL4210242)
Affinity DataKi:  153nMAssay Description:Binding affinity to human ERalpha LBD after 2 hrs in absence of light by competitive fluorometric binding assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/16/2020
Entry Details Article
PubMed
TargetEstrogen receptor beta(Human)
Wuhan University

Curated by ChEMBL
LigandPNGBDBM50458901(CHEMBL4210242)
Affinity DataKi:  303nMAssay Description:Binding affinity to human ERbeta LBD after 2 hrs in absence of light by competitive fluorometric binding assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/16/2020
Entry Details Article
PubMed