null

SMILES Cc1cccc(\C=C\Cc2ccc(\C=C\C(O)=O)cc2)c1OCc1ccccc1

InChI Key InChIKey=XSUQLASBFHZVGW-XMSMBIEGSA-N

  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 = 50370463   

TargetProstaglandin E2 receptor EP2 subtype(Homo sapiens (Human))
Merck Frosst Centre for Therapeutic Research

Curated by ChEMBL
LigandPNGBDBM50370463(CHEMBL1237300)copy SMILEScopy InChI
Affinity DataKi:  1.70E+3nMAssay Description:Binding affinity for human prostanoid EP2 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26H4J51PubMed
TargetProstaglandin E2 receptor EP3 subtype(Homo sapiens (Human))
Merck Frosst Centre for Therapeutic Research

Curated by ChEMBL
LigandPNGBDBM50370463(CHEMBL1237300)copy SMILEScopy InChI
Affinity DataKi:  2.90E+3nMAssay Description:Binding affinity for human prostanoid EP3 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26H4J51PubMed
TargetProstaglandin E2 receptor EP4 subtype(Homo sapiens (Human))
Merck Frosst Centre for Therapeutic Research

Curated by ChEMBL
LigandPNGBDBM50370463(CHEMBL1237300)copy SMILEScopy InChI
Affinity DataKi:  5.50E+3nMAssay Description:Binding affinity for human prostanoid EP4 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26H4J51PubMed
TargetProstaglandin E2 receptor EP1 subtype(Homo sapiens (Human))
Merck Frosst Centre for Therapeutic Research

Curated by ChEMBL
LigandPNGBDBM50370463(CHEMBL1237300)copy SMILEScopy InChI
Affinity DataKi: >3.00E+4nMAssay Description:Binding affinity for human prostanoid EP1 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26H4J51PubMed