BDBM50366664 CHEMBL1627353

SMILES C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@@H]2O)[C@H](Sc1ccc(Br)cc1)C(O)c1cc(O)ccc31

InChI Key InChIKey=XEKKTAYAEIHJEA-UHFFFAOYSA-N

Data  2 IC50  1 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 3 hits for monomerid = 50366664   

TargetEstrogen receptor(Human)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50366664(CHEMBL1627353)
Affinity DataEC50:  7nMAssay Description:Agonist effect on transcriptional activation in MCF-7 cells expressing estrogen receptor alphaMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/1/2012
Entry Details Article
PubMed
TargetEstrogen receptor beta(Human)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50366664(CHEMBL1627353)
Affinity DataIC50: 63nMAssay Description:Displacement of [3H]17-beta-estradiol from human Estrogen receptor betaMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/1/2012
Entry Details Article
PubMed
TargetEstrogen receptor(Human)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50366664(CHEMBL1627353)
Affinity DataIC50: 397nMAssay Description:Agonist effect on transcriptional activation in MCF-7 cells expressing estrogen receptor alphaMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/1/2012
Entry Details Article
PubMed