BDBM50583627 CHEMBL5075221

SMILES CC[C@@H](Cc1ccc(cc1)C(=O)NCc1ccc(OC)cc1C(F)(F)F)C(O)=O

InChI Key InChIKey=VPAHYLNIDWFBPW-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 = 50583627   

TargetPeroxisome proliferator-activated receptor gamma(Human)
Goethe University

Curated by ChEMBL
LigandPNGBDBM50583627(CHEMBL5075221)
Affinity DataEC50:  5.20E+3nMAssay Description:Agonist activity at recombinant N-terminal His6 -tagged GFP fused PPARgamma LBD (unknown origin) (203 to 477 residues) expressed in Escherichia cell ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/6/2023
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Human)
Goethe University

Curated by ChEMBL
LigandPNGBDBM50583627(CHEMBL5075221)
Affinity DataEC50:  240nMAssay Description:Inhibition of recombinant human C-terminal sEH (222 to 555 residues) expressed in Escherichia coli BL21-DE3 using PHOME as substrate assessed as redu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/6/2023
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Goethe University

Curated by ChEMBL
LigandPNGBDBM50583627(CHEMBL5075221)
Affinity DataEC50:  2.50E+3nMAssay Description:Agonist activity at human GAL4 DBD-fused PPARgamma LBD (203 to 505 residues) transfected in HEK293T cells assessed as fold activation incubated for 1...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/6/2023
Entry Details Article
PubMed