BDBM50159765 (E)-3-{2-[3-(2-Benzyloxy-3-methoxy-phenyl)-propyl]-phenyl}-acrylic acid::CHEMBL181691

SMILES COc1cccc(CCCc2ccccc2\C=C\C(O)=O)c1OCc1ccccc1

InChI Key InChIKey=VERBESGORYHQNN-UHFFFAOYSA-N

Data  4 KI

  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 4 hits for monomerid = 50159765   

TargetProstaglandin E2 receptor EP3 subtype(Human)
Merck Frosst Centre For Therapeutic Research

Curated by ChEMBL
LigandPNGBDBM50159765((E)-3-{2-[3-(2-Benzyloxy-3-methoxy-phenyl)-propyl]...)
Affinity DataKi:  19nMAssay Description:Binding affinity for human prostanoid EP3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/2/2012
Entry Details Article
PubMed
TargetProstaglandin E2 receptor EP2 subtype(Human)
Merck Frosst Centre For Therapeutic Research

Curated by ChEMBL
LigandPNGBDBM50159765((E)-3-{2-[3-(2-Benzyloxy-3-methoxy-phenyl)-propyl]...)
Affinity DataKi:  1.10E+3nMAssay Description:Binding affinity for human prostanoid EP2 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/2/2012
Entry Details Article
PubMed
TargetProstaglandin E2 receptor EP4 subtype(Human)
Merck Frosst Centre For Therapeutic Research

Curated by ChEMBL
LigandPNGBDBM50159765((E)-3-{2-[3-(2-Benzyloxy-3-methoxy-phenyl)-propyl]...)
Affinity DataKi:  4.30E+3nMAssay Description:Binding affinity for human prostanoid EP4 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/2/2012
Entry Details Article
PubMed
TargetProstaglandin E2 receptor EP1 subtype(Human)
Merck Frosst Centre For Therapeutic Research

Curated by ChEMBL
LigandPNGBDBM50159765((E)-3-{2-[3-(2-Benzyloxy-3-methoxy-phenyl)-propyl]...)
Affinity DataKi: >9.00E+3nMAssay Description:Binding affinity for human prostanoid EP1 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/2/2012
Entry Details Article
PubMed