BDBM50127936 5-{4-[3-(4-Phenoxy-phenoxy)-propoxy]-phenyl}-thiazolidine-2,4-dione::CHEMBL50259

SMILES Oc1[nH]c(=O)sc1-c1ccc(OCCCOc2ccc(Oc3ccccc3)cc2)cc1

InChI Key InChIKey=SYZMDAZCXPOTBB-UHFFFAOYSA-N

Data  3 IC50

  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 = 50127936   

TargetPeroxisome proliferator-activated receptor gamma(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50127936BDBM50127936(5-{4-[3-(4-Phenoxy-phenoxy)-propoxy]-phenyl}-thiaz...)
Affinity DataIC50: 1.50E+4nMAssay Description:In vitro binding affinity against human PPAR gamma (peroxisome proliferator-activated gamma receptor)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor alpha(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50127936BDBM50127936(5-{4-[3-(4-Phenoxy-phenoxy)-propoxy]-phenyl}-thiaz...)
Affinity DataIC50: 5.00E+4nMAssay Description:In vitro binding affinity against human PPAR alpha (peroxisome proliferator-activated alpha receptor)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor delta(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50127936BDBM50127936(5-{4-[3-(4-Phenoxy-phenoxy)-propoxy]-phenyl}-thiaz...)
Affinity DataIC50: 5.00E+4nMAssay Description:In vitro binding affinity against human PPAR delta (peroxisome proliferator-activated delta receptor)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed