BDBM50372119 CHEMBL271241

SMILES CCCCCCCN(CCc1ccc(O[C@](C)(CC)C(O)=O)cc1)C(=O)Nc1ccc(F)cc1F

InChI Key InChIKey=VGSJXSLGVQINOL-HHHXNRCGSA-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 = 50372119   

TargetPeroxisome proliferator-activated receptor alpha(Homo sapiens (Human))
Bristol-Myers Squibb Research And Development

Curated by ChEMBL
LigandPNGBDBM50372119(CHEMBL271241)
Affinity DataIC50:  740nMAssay Description:Inhibition of PPARalphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor alpha(Homo sapiens (Human))
Bristol-Myers Squibb Research And Development

Curated by ChEMBL
LigandPNGBDBM50372119(CHEMBL271241)
Affinity DataEC50:  45nMAssay Description:Agonist activity at PPARalpha in HEK293 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Bristol-Myers Squibb Research And Development

Curated by ChEMBL
LigandPNGBDBM50372119(CHEMBL271241)
Affinity DataEC50:  243nMAssay Description:Agonist activity at PPARgamma in HEK293 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Bristol-Myers Squibb Research And Development

Curated by ChEMBL
LigandPNGBDBM50372119(CHEMBL271241)
Affinity DataIC50:  600nMAssay Description:Inhibition of PPARgammaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed