BDBM50173654 1-(4-Chloro-phenyl)-2-(4-hydroxy-phenyl)-3H-inden-5-ol::CHEMBL364442

SMILES Oc1ccc(cc1)C1=C(c2ccc(O)cc2C1)c1ccc(Cl)cc1

InChI Key InChIKey=KYKWZUMHVAPNQH-UHFFFAOYSA-N

Data  2 KI  1 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50173654   

TargetEstrogen receptor beta(Homo sapiens (Human))
University Of California

Curated by ChEMBL
LigandPNGBDBM50173654(1-(4-Chloro-phenyl)-2-(4-hydroxy-phenyl)-3H-inden-...)
Affinity DataKi:  0.490nMAssay Description:Antagonistic activity against estrogen receptor beta in presence of 0.1 nM estradiolMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor(Homo sapiens (Human))
University Of California

Curated by ChEMBL
LigandPNGBDBM50173654(1-(4-Chloro-phenyl)-2-(4-hydroxy-phenyl)-3H-inden-...)
Affinity DataKi:  24nMAssay Description:Antagonistic activity against estrogen receptor alpha in presence of 0.1 nM estradiolMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor(Homo sapiens (Human))
University Of California

Curated by ChEMBL
LigandPNGBDBM50173654(1-(4-Chloro-phenyl)-2-(4-hydroxy-phenyl)-3H-inden-...)
Affinity DataEC50:  17nMAssay Description:Transcriptional activation of estrogen receptor alpha in U2OS cell using estrogen-regulated luciferase reporter gene plasmid upon incubation for 20-3...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed