BDBM50312392 2-(4-((4-(biphenyl-4-yl)thiazol-2-yl)methoxy)-2-methylphenoxy)acetic acid::CHEMBL1079489

SMILES Cc1cc(OCc2nc(cs2)-c2ccc(cc2)-c2ccccc2)ccc1OCC(O)=O

InChI Key InChIKey=AXHXSOYRYGSQHK-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 = 50312392   

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

Curated by ChEMBL
LigandPNGBDBM50312392(2-(4-((4-(biphenyl-4-yl)thiazol-2-yl)methoxy)-2-me...)
Affinity DataEC50:  340nMAssay Description:Agonist activity at human PPARdelta ligand binding domain expressed in human 293T cells co-transfected with Gal4-DBD by luciferase transactivation as...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor alpha(Human)
The Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50312392(2-(4-((4-(biphenyl-4-yl)thiazol-2-yl)methoxy)-2-me...)
Affinity DataEC50:  480nMAssay Description:Agonist activity at human PPARalpha ligand binding domain expressed in human 293T cells co-transfected with Gal4-DBD by luciferase transactivation as...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
The Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50312392(2-(4-((4-(biphenyl-4-yl)thiazol-2-yl)methoxy)-2-me...)
Affinity DataEC50: >1.00E+4nMAssay Description:Agonist activity at human PPARgamma ligand binding domain expressed in human 293T cells co-transfected with Gal4-DBD by luciferase transactivation as...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed