BDBM50189069 (S)(-)-9a-butyl-6-thiophen-2-yl-8,9,9a,10-tetrahydro-3H-1,2,3-triaza-cyclopenta[a]fluoren-7-one::CHEMBL214692

SMILES CCCC[C@]12Cc3c(ccc4nn[nH]c34)C1=C(c1cccs1)C(=O)CC2

InChI Key InChIKey=TZACYAAFEOUQNL-NRFANRHFSA-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 = 50189069   

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

Curated by ChEMBL
LigandPNGBDBM50189069((S)(-)-9a-butyl-6-thiophen-2-yl-8,9,9a,10-tetrahyd...)
Affinity DataIC50:  34nMAssay Description:Binding affinity to human recombinant ERalpha by scintillation proximity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50189069((S)(-)-9a-butyl-6-thiophen-2-yl-8,9,9a,10-tetrahyd...)
Affinity DataIC50:  2.30nMAssay Description:Binding affinity to human recombinant ERbeta by scintillation proximity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50189069((S)(-)-9a-butyl-6-thiophen-2-yl-8,9,9a,10-tetrahyd...)
Affinity DataEC50:  0.960nMAssay Description:Agonist activity at human recombinant ERbeta expressed in HEK293 cells by alkaline phosphatase reporter gene transactivation assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50189069((S)(-)-9a-butyl-6-thiophen-2-yl-8,9,9a,10-tetrahyd...)
Affinity DataEC50:  79nMAssay Description:Agonist activity at human recombinant ERalpha expressed in HEK293 cells by alkaline phosphatase reporter gene transactivation assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed