BDBM28763 (2S)-2-(4-{2-[1,3-benzoxazol-2-yl(heptyl)amino]ethyl}phenoxy)-2-methylbutanoic acid::LT127 (ureidofibrate derivative), (S)-1
SMILES CCCCCCCN(CCc1ccc(O[C@@](C)(CC)C(O)=O)cc1)c1nc2ccccc2o1
InChI Key InChIKey=QPKIEBNVIOELIR-MHZLTWQESA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 6 hits for monomerid = 28763
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Istituto Tumori&Quot;Giovanni Paolo Ii&Quot
Curated by ChEMBL
Istituto Tumori&Quot;Giovanni Paolo Ii&Quot
Curated by ChEMBL
Affinity DataKi: 971nMAssay Description:Displacement of [3H]rosiglitazone from N-terminal His-tagged human PPARgamma ligand binding domain expressed in Escherichia coli BL21 DE3 cells by sc...More data for this Ligand-Target Pair
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Istituto Tumori&Quot;Giovanni Paolo Ii&Quot
Curated by ChEMBL
Istituto Tumori&Quot;Giovanni Paolo Ii&Quot
Curated by ChEMBL
Affinity DataKi: 971nM ΔG°: -8.11kcal/molepH: 7.5 T: 2°CAssay Description:The scintillation proximity assay was performed in 96-well plates containing polylysine-coated yttrium silicate beads, His-PPARgamma-LBD, and [3H]ros...More data for this Ligand-Target Pair
TargetPeroxisome proliferator-activated receptor alpha(Homo sapiens (Human))
Istituto Tumori&Quot;Giovanni Paolo Ii&Quot
Curated by ChEMBL
Istituto Tumori&Quot;Giovanni Paolo Ii&Quot
Curated by ChEMBL
Affinity DataEC50: 56nMAssay Description:Agonist activity at human GAL4-fused PPARalpha ligand binding domain expressed in HepG2 cells after 20 hrs by luciferase reporter gene transactivatio...More data for this Ligand-Target Pair
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Istituto Tumori&Quot;Giovanni Paolo Ii&Quot
Curated by ChEMBL
Istituto Tumori&Quot;Giovanni Paolo Ii&Quot
Curated by ChEMBL
Affinity DataKd: 2.00E+3nMAssay 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&Quot;Giovanni Paolo Ii&Quot
Curated by ChEMBL
Istituto Tumori&Quot;Giovanni Paolo Ii&Quot
Curated by ChEMBL
Affinity DataKd: 1.98E+3nM EC50: 593nMpH: 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
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Istituto Tumori&Quot;Giovanni Paolo Ii&Quot
Curated by ChEMBL
Istituto Tumori&Quot;Giovanni Paolo Ii&Quot
Curated by ChEMBL
Affinity DataEC50: 590nMAssay Description:Agonist activity at human GAL4-fused PPARgamma ligand binding domain expressed in HepG2 cells after 20 hrs by luciferase reporter gene transactivatio...More data for this Ligand-Target Pair