BDBM50184666 CHEMBL379123::[4-([1,1';3',1'']terphenyl-5'-ylmet hoxy)-phenoxy]-acetic acid

SMILES OC(=O)COc1ccc(OCc2cc(cc(c2)-c2ccccc2)-c2ccccc2)cc1

InChI Key InChIKey=DWUCUTJBFNCJRL-UHFFFAOYSA-N

Data  3 EC50

  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 = 50184666   

TargetPeroxisome proliferator-activated receptor alpha(Human)
The Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50184666([4-([1,1';3',1'']terphenyl-5'-ylmet hoxy)-phenoxy]...)
Affinity DataEC50: >1.00E+4nMAssay Description:Effect on human PPARalpha transactivation in 293T cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor delta(Human)
The Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50184666([4-([1,1';3',1'']terphenyl-5'-ylmet hoxy)-phenoxy]...)
Affinity DataEC50:  970nMAssay Description:Effect on human PPARdelta transactivation in 293T cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
The Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50184666([4-([1,1';3',1'']terphenyl-5'-ylmet hoxy)-phenoxy]...)
Affinity DataEC50:  1.20E+3nMAssay Description:Effect on human PPARgamma transactivation in 293T cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed