BDBM50134529 3-{2-[5-(2-Benzyloxy-phenyl)-thiophen-2-yl]-phenyl}-propionic acid::CHEMBL125110

SMILES OC(=O)CCc1ccccc1-c1ccc(s1)-c1ccccc1OCc1ccccc1

InChI Key InChIKey=ASVCOSIDAVCXKO-UHFFFAOYSA-N

Data  4 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50134529   

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

Curated by ChEMBL
LigandPNGBDBM50134529(3-{2-[5-(2-Benzyloxy-phenyl)-thiophen-2-yl]-phenyl...)
Affinity DataKi:  520nMAssay Description:Affinity at human Prostanoid EP3 receptor in the human embryonic kidney (HEK) 293 cell line.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin E2 receptor EP4 subtype(Homo sapiens (Human))
Merck Frosst Centre For Therapeutic Research

Curated by ChEMBL
LigandPNGBDBM50134529(3-{2-[5-(2-Benzyloxy-phenyl)-thiophen-2-yl]-phenyl...)
Affinity DataKi:  1.10E+3nMAssay Description:Affinity at human Prostanoid EP4 receptor in the human embryonic kidney (HEK) 293 cell line.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin E2 receptor EP2 subtype(Homo sapiens (Human))
Merck Frosst Centre For Therapeutic Research

Curated by ChEMBL
LigandPNGBDBM50134529(3-{2-[5-(2-Benzyloxy-phenyl)-thiophen-2-yl]-phenyl...)
Affinity DataKi:  4.10E+3nMAssay Description:Affinity at human Prostanoid EP2 receptor in the human embryonic kidney (HEK) 293 cell line.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin E2 receptor EP1 subtype(Homo sapiens (Human))
Merck Frosst Centre For Therapeutic Research

Curated by ChEMBL
LigandPNGBDBM50134529(3-{2-[5-(2-Benzyloxy-phenyl)-thiophen-2-yl]-phenyl...)
Affinity DataKi:  2.70E+4nMAssay Description:Affinity at human Prostanoid EP1 receptor in the human embryonic kidney (HEK) 293 cell line.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed