BDBM50242859 CHEMBL4072125

SMILES CCOC(Cc1ccc(Oc2ccc(OCc3ccccc3)cc2)cc1)C(O)=O

InChI Key InChIKey=FOOAUPXVHNXVBV-UHFFFAOYSA-N

Data  3 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 = 50242859   

TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50242859(CHEMBL4072125)
Affinity DataEC50:  1.80E+4nMAssay Description:Ability to displace [3H]quipazine binding to 5-hydroxytryptamine 3 receptor sites in NG 108-15.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor delta(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50242859(CHEMBL4072125)
Affinity DataEC50:  3.10E+4nMAssay Description:Compound was evaluated for its ability to displace [3H]quipazine binding to 5-hydroxytryptamine 3 receptor sites in NG 108-15 .More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor alpha(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50242859(CHEMBL4072125)
Affinity DataEC50:  5.40E+3nMAssay Description:Ability to displace [3H]quipazine binding to 5-hydroxytryptamine 3 receptor sites in NG 108-15.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed