null

SMILES CC1=CC[C@@]2(CO)COC([C@@H]1C2)c1ccc(O)cc1

InChI Key InChIKey=XXIFNRNIQJKFLP-UYSNPLJNSA-N

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

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50128414   

TargetEstrogen receptor(Homo sapiens (Human))
Bayer Corporation

Curated by ChEMBL
LigandPNGBDBM50128414(4-((1R,5R)-5-Hydroxymethyl-8-methyl-3-oxa-bicyclo[...)copy SMILEScopy InChI
Affinity DataIC50: 3.20E+3nMAssay 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
LigandPNGBDBM50128414(4-((1R,5R)-5-Hydroxymethyl-8-methyl-3-oxa-bicyclo[...)copy SMILEScopy InChI
Affinity DataEC50:  20nMAssay 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
LigandPNGBDBM50128414(4-((1R,5R)-5-Hydroxymethyl-8-methyl-3-oxa-bicyclo[...)copy SMILEScopy InChI
Affinity DataIC50: 850nMAssay Description:In vitro binding affinity for estrogen receptor betaMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29K49MKPubMed