BDBM50187949 CHEMBL211953::rac-6,9a-diethyl-8,9,9a,10-tetrahydroindeno[2,1-e]indazol-7(3H)-one

SMILES CCC1=C2c3ccc4[nH]ncc4c3CC2(CC)CCC1=O

InChI Key InChIKey=LTTCWZPUBNOMTJ-UHFFFAOYSA-N

Data  2 IC50  2 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 4 hits for monomerid = 50187949   

TargetEstrogen receptor beta(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50187949(CHEMBL211953 | rac-6,9a-diethyl-8,9,9a,10-tetrahyd...)
Affinity DataEC50:  1.70nMAssay Description:Agonist activity at human ERbeta transfected in HEK293 cells assessed as transactivation of alkaline phosphatase reporter geneMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50187949(CHEMBL211953 | rac-6,9a-diethyl-8,9,9a,10-tetrahyd...)
Affinity DataEC50:  59nMAssay Description:Agonist activity at human ERalpha transfected in HEK293 cells assessed as transactivation of alkaline phosphatase reporter geneMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50187949(CHEMBL211953 | rac-6,9a-diethyl-8,9,9a,10-tetrahyd...)
Affinity DataIC50:  223nMAssay Description:Binding affinity to human ERalphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50187949(CHEMBL211953 | rac-6,9a-diethyl-8,9,9a,10-tetrahyd...)
Affinity DataIC50:  4nMAssay Description:Binding affinity to human ERbetaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed