null

SMILES [#6]\[#6](-[#6])=[#6]/[#6]=[#6]/[#6@H]-1-[#6]-[#6]-[#6](=O)-[#7]1-[#6]-[#6]-c1ccc(cc1)-[#6](-[#8])=O

InChI Key InChIKey=HHOFHJTWHYKKJJ-RCFWFJCLSA-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 3 hits for monomerid = 50213976   

TargetProstaglandin E2 receptor EP4 subtype(Homo sapiens (Human))
EMD Serono Research Institute

Curated by ChEMBL
LigandPNGBDBM50213976((R)-4-(2-(2-(4-methylpenta-1,3-dienyl)-5-oxopyrrol...)copy SMILEScopy InChI
Affinity DataKi:  45nMAssay Description:Displacement of [3H]PGE2 from human EP4 receptor expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RF5VVCPubMed
TargetProstaglandin E2 receptor EP2 subtype(Homo sapiens (Human))
EMD Serono Research Institute

Curated by ChEMBL
LigandPNGBDBM50213976((R)-4-(2-(2-(4-methylpenta-1,3-dienyl)-5-oxopyrrol...)copy SMILEScopy InChI
Affinity DataKi:  1.85E+3nMAssay Description:Displacement of [3H]PGE2 from human EP2 receptor expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RF5VVCPubMed
TargetProstaglandin E2 receptor EP4 subtype(Homo sapiens (Human))
EMD Serono Research Institute

Curated by ChEMBL
LigandPNGBDBM50213976((R)-4-(2-(2-(4-methylpenta-1,3-dienyl)-5-oxopyrrol...)copy SMILEScopy InChI
Affinity DataEC50:  4nMAssay Description:Agonist activity at EP4 receptor expressed in HEK293 cells assessed as cAMP accumulationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RF5VVCPubMed