null

SMILES CCCCCCCN(CCc1ccc(O[C@](C)(CC)C(O)=O)cc1)c1nc2ccccc2o1

InChI Key InChIKey=QPKIEBNVIOELIR-HHHXNRCGSA-N

PDB links: 1 PDB ID matches this monomer. 1 PDB ID contains this monomer as substructures.

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 28762   

TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Istituto Tumori"Giovanni Paolo II"

Curated by ChEMBL
LigandPNGBDBM28762((2R)-2-(4-{2-[1,3-benzoxazol-2-yl(heptyl)amino]eth...)copy SMILEScopy InChI
Affinity DataKd:  270nMAssay Description:Binding affinity to PPARgamma ligand binding domain by isothermal titration calorimetryMore data for this Ligand-Target Pair
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Istituto Tumori"Giovanni Paolo II"

Curated by ChEMBL
LigandPNGBDBM28762((2R)-2-(4-{2-[1,3-benzoxazol-2-yl(heptyl)amino]eth...)copy SMILEScopy InChI
Affinity DataKd:  685nM EC50:  73.3nMpH: 7.5 T: 2°CAssay Description:Kd values were obtained by incubating His-PPARgamma-LBD with biotinylated peptide, europium-labeled anti-histidine antibody, and allophycocyanin-labe...More data for this Ligand-Target Pair