BDBM50181910 2-(6-(3-(4-(4-fluorobenzoyl)-2-propylphenoxy)propoxy)-1H-indol-1-yl)acetic acid::CHEMBL202140
SMILES CCCc1cc(ccc1OCCCOc1ccc2ccn(CC(O)=O)c2c1)C(=O)c1ccc(F)cc1
InChI Key InChIKey=CHUOXAKJPAYADI-UHFFFAOYSA-N
Data 6 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 6 hits for monomerid = 50181910
TargetPeroxisome proliferator-activated receptor delta(Human)
National Health Research Institutes
Curated by ChEMBL
National Health Research Institutes
Curated by ChEMBL
Affinity DataIC50: 7.62E+3nMAssay Description:Displacement of [3H]L-783483 from human PPAR delta by SPA assayMore data for this Ligand-Target Pair
TargetPeroxisome proliferator-activated receptor alpha(Human)
National Health Research Institutes
Curated by ChEMBL
National Health Research Institutes
Curated by ChEMBL
Affinity DataIC50: 1.05E+3nMAssay Description:Displacement of [3H]L-783483 from human PPAR alpha by SPA assayMore data for this Ligand-Target Pair
TargetPeroxisome proliferator-activated receptor gamma(Human)
National Health Research Institutes
Curated by ChEMBL
National Health Research Institutes
Curated by ChEMBL
Affinity DataIC50: 1.29E+3nMAssay Description:Displacement of [3H]rosiglitazone from human PPAR gamma by SPA assayMore data for this Ligand-Target Pair
TargetPeroxisome proliferator-activated receptor alpha(Human)
National Health Research Institutes
Curated by ChEMBL
National Health Research Institutes
Curated by ChEMBL
Affinity DataIC50: 1.05E+3nMAssay Description:Agonist activity at PPARalphaMore data for this Ligand-Target Pair
TargetPeroxisome proliferator-activated receptor delta(Human)
National Health Research Institutes
Curated by ChEMBL
National Health Research Institutes
Curated by ChEMBL
Affinity DataIC50: 7.62E+3nMAssay Description:Agonist activity at PPARdeltaMore data for this Ligand-Target Pair
TargetPeroxisome proliferator-activated receptor gamma(Human)
National Health Research Institutes
Curated by ChEMBL
National Health Research Institutes
Curated by ChEMBL
Affinity DataIC50: 1.29E+3nMAssay Description:Agonist activity at PPARgammaMore data for this Ligand-Target Pair