BDBM50372120 CHEMBL272774

SMILES COc1ccc(cc1)N1[C@H]([C@@H](Cc2ccc(OCCc3nc(oc3C)-c3ccccc3)cc2)C1=O)C(O)=O

InChI Key InChIKey=WTRWFOXPPRLKFP-UHFFFAOYSA-N

Data  2 IC50  1 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 = 50372120   

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

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50372120BDBM50372120(CHEMBL272774)
Affinity DataIC50: 3.40E+3nMAssay Description:Inhibition of PPARgammaMore 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

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50372120BDBM50372120(CHEMBL272774)
Affinity DataEC50: >7.50E+3nMAssay Description:Agonist activity at PPARalpha in HEK293 cells 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

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50372120BDBM50372120(CHEMBL272774)
Affinity DataIC50: 1.50E+4nMAssay Description:Inhibition of PPARalphaMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/15/2012
Entry Details Article
PubMed