BDBM50427834 CHEMBL2326068

SMILES C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@@H]2O)[C@H](CCCCc1cn(CC2COc4ccccc4O2)nn1)Cc1cc(O)ccc31

InChI Key InChIKey=AWCSWPAAFIXQFA-GWCQTFJGSA-N

Data  3 IC50

  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 = 50427834   

TargetSteroid hormone receptor ERR1(Homo sapiens (Human))
University Of Kansas Medical Center

Curated by ChEMBL
LigandPNGBDBM50427834(CHEMBL2326068)
Affinity DataIC50:  24nMAssay Description:Displacement of [3H]E2 from human recombinant ERalpha receptor after overnight incubation by liquid scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIsoform 1 of Steroid hormone receptor ERR2 (ERRbeta2-delta10)(Homo sapiens (Human))
University Of Kansas Medical Center

Curated by ChEMBL
LigandPNGBDBM50427834(CHEMBL2326068)
Affinity DataIC50:  41nMAssay Description:Displacement of [3H]E2 from human recombinant ERbeta receptor after overnight incubation by liquid scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSteroid hormone receptor ERR1(Homo sapiens (Human))
University Of Kansas Medical Center

Curated by ChEMBL
LigandPNGBDBM50427834(CHEMBL2326068)
Affinity DataIC50:  50nMAssay Description:Antagonist activity at ERalpha receptor in human MCF7 cells assessed as inhibition of cell growth after 6 days by crystal violet staining methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed