BDBM50377308 CHEMBL445942

SMILES Cc1oc(nc1CCOc1cccc(c1)C1CN(CCC1CC(O)=O)C(=O)Oc1ccccc1)-c1ccccc1

InChI Key InChIKey=IIGKUFIQZADLCW-UHFFFAOYSA-N

Data  2 IC50  2 EC50

  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 = 50377308   

TargetPeroxisome proliferator-activated receptor gamma(Human)
Bristol-Myers Squibb R & D

Curated by ChEMBL
LigandPNGBDBM50377308(CHEMBL445942)
Affinity DataIC50: 8.12E+3nMAssay Description:Binding affinity at human PPARalpha by fluorescence polarizationMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/15/2012
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor alpha(Human)
Bristol-Myers Squibb R & D

Curated by ChEMBL
LigandPNGBDBM50377308(CHEMBL445942)
Affinity DataEC50:  1.29E+3nMAssay Description:Agonist activity at human PPARgamma expressed in HEK293 cells assessed as luciferase activity by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/15/2012
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Bristol-Myers Squibb R & D

Curated by ChEMBL
LigandPNGBDBM50377308(CHEMBL445942)
Affinity DataEC50:  170nMAssay Description:Agonist activity at human PPARalpha expressed in HEK293 cells assessed as luciferase activity by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/15/2012
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor alpha(Human)
Bristol-Myers Squibb R & D

Curated by ChEMBL
LigandPNGBDBM50377308(CHEMBL445942)
Affinity DataIC50: 7.69E+3nMAssay Description:Binding affinity at human PPARalpha by fluorescence polarizationMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/15/2012
Entry Details Article
PubMed