null

SMILES O=C1CCC2(Cc3ccccc3)Cc3c(ccc4[nH]ncc34)C2=C1

InChI Key InChIKey=RSNGIABRBFWZKL-UHFFFAOYSA-N

  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 = 50194078   

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

Curated by ChEMBL
LigandPNGBDBM50194078(9a-benzyl-8,9,9a,10-tetrahydroindeno[2,1-e]indazol...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Binding affinity to human ER alphaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DB81GHPubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
IRBM (Merck Research Laboratories Rome)

Curated by ChEMBL
LigandPNGBDBM50194078(9a-benzyl-8,9,9a,10-tetrahydroindeno[2,1-e]indazol...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Binding affinity to human ER betaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DB81GHPubMed
TargetEstrogen receptor(Homo sapiens (Human))
IRBM (Merck Research Laboratories Rome)

Curated by ChEMBL
LigandPNGBDBM50194078(9a-benzyl-8,9,9a,10-tetrahydroindeno[2,1-e]indazol...)copy SMILEScopy InChI
Affinity DataIC50: 3.90E+3nMAssay Description:Binding affinity to ERalpha L384M/M421G mutantMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DB81GHPubMed