null

SMILES C[C@H]1CCN(CCOc2ccc(cc2)[C@@H]2Oc3ccc(O)c(F)c3[C@@H](C)[C@@H]2c2ccc(O)cc2)C1

InChI Key InChIKey=KREZVKKCLKOMEF-IWKAXJDJSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50162801   

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

Curated by ChEMBL
LigandPNGBDBM50162801((2R,3R,4S)-5-Fluoro-3-(4-hydroxy-phenyl)-4-methyl-...)copy SMILEScopy InChI
Affinity DataIC50: 0.800nMAssay Description:Inhibition of estrogen receptor alphaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S46RFBPubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50162801((2R,3R,4S)-5-Fluoro-3-(4-hydroxy-phenyl)-4-methyl-...)copy SMILEScopy InChI
Affinity DataIC50: 16nMAssay Description:Inhibition of estrogen receptor betaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S46RFBPubMed