BDBM50370469 CHEMBL1237303

SMILES CC(=O)c1ccc(OCc2ccccc2)c(C\C=C\c2ccccc2C=CC(O)=O)c1

InChI Key InChIKey=JPPPPFROUMRPCE-UHFFFAOYSA-N

Data  4 KI

  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 4 hits for monomerid = 50370469   

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

Curated by ChEMBL
LigandPNGBDBM50370469(CHEMBL1237303)
Affinity DataKi:  260nMAssay 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 EP4 subtype(Human)
Merck Frosst Centre For Therapeutic Research

Curated by ChEMBL
LigandPNGBDBM50370469(CHEMBL1237303)
Affinity DataKi:  830nMAssay 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
LigandPNGBDBM50370469(CHEMBL1237303)
Affinity DataKi:  2.80E+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
TargetProstaglandin E2 receptor EP2 subtype(Human)
Merck Frosst Centre For Therapeutic Research

Curated by ChEMBL
LigandPNGBDBM50370469(CHEMBL1237303)
Affinity DataKi:  8.70E+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