BDBM50349832 CHEMBL1813202

SMILES CCOc1cc(ccc1CCc1ccc(C[C@H](CC)C(O)=O)cc1)N1C(=O)c2ccccc2C1=O

InChI Key InChIKey=PMFWRAGPLVIDGB-NRFANRHFSA-N

Data  3 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50349832   

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

Curated by ChEMBL
LigandPNGBDBM50349832(CHEMBL1813202)
Affinity DataEC50:  3.20E+3nMAssay Description:Agonist activity at PPARgamma expressed in HEK293 after 8 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor alpha(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM50349832(CHEMBL1813202)
Affinity DataEC50:  1.70E+3nMAssay Description:Agonist activity at human PPARalpha expressed in HEK293 after 8 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor delta(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM50349832(CHEMBL1813202)
Affinity DataEC50:  1.90E+3nMAssay Description:Agonist activity at PPARdelta expressed in HEK293 after 8 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed