null

SMILES OC[C@]12CC[C@H]([C@H](C1)C=CC2)c1ccc(O)cc1

InChI Key InChIKey=RTWQEZPGFVTNAW-PXWJKWRZSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50128415   

TargetEstrogen receptor(Homo sapiens (Human))
Bayer Corporation

Curated by ChEMBL
LigandPNGBDBM50128415(4-((1R,2R,5S)-5-Hydroxymethyl-bicyclo[3.3.1]non-7-...)copy SMILEScopy InChI
Affinity DataIC50: 550nMAssay Description:In vitro binding affinity for estrogen receptor alphaMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29K49MKPubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
Bayer Corporation

Curated by ChEMBL
LigandPNGBDBM50128415(4-((1R,2R,5S)-5-Hydroxymethyl-bicyclo[3.3.1]non-7-...)copy SMILEScopy InChI
Affinity DataEC50: <10nMAssay Description:Percent agonistic activity for estrogen-induced pS2 expression in MCF-7 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29K49MKPubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
Bayer Corporation

Curated by ChEMBL
LigandPNGBDBM50128415(4-((1R,2R,5S)-5-Hydroxymethyl-bicyclo[3.3.1]non-7-...)copy SMILEScopy InChI
Affinity DataIC50: 75nMAssay Description:In vitro binding affinity for estrogen receptor betaMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29K49MKPubMed