Compile Data Set for Download or QSAR
Report error Found 18 Enz. Inhib. hit(s) with all data for entry = 50035108
LigandChemical structure of BindingDB Monomer ID 50085584BDBM50085584(5-(4-{2-[1-(6-Phenyl-pyridin-3-yl)-eth-(E)-ylidene...)
Affinity DataEC50:  190nMAssay Description:Peroxisome proliferator activated receptor gamma agonistic activity in HepG2 cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/2/2012
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085575BDBM50085575(5-(4-{2-[1-Biphenyl-3-yl-eth-(E)-ylideneaminooxy]-...)
Affinity DataEC50:  330nMAssay Description:Peroxisome proliferator activated receptor gamma agonistic activity in HepG2 cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/2/2012
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085587BDBM50085587(5-(4-{2-[1-Biphenyl-4-yl-eth-(E)-ylideneaminooxy]-...)
Affinity DataEC50:  400nMAssay Description:Peroxisome proliferator activated receptor gamma agonistic activity in HepG2 cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/2/2012
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085581BDBM50085581(5-(4-{2-[1-(4-Pyridin-2-yl-phenyl)-eth-(E)-ylidene...)
Affinity DataEC50:  640nMAssay Description:Peroxisome proliferator activated receptor gamma agonistic activity in HepG2 cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/2/2012
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 28681BDBM28681(cid_5281055 | [3H]rosiglitazone | CHEMBL121 | ROSI...)
Affinity DataEC50:  730nMAssay Description:Peroxisome proliferator activated receptor gamma agonistic activity in HepG2 cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/2/2012
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085576BDBM50085576(5-(4-{2-[1-(4-Pyridin-3-yl-phenyl)-eth-(E)-ylidene...)
Affinity DataEC50:  800nMAssay Description:Peroxisome proliferator activated receptor gamma agonistic activity in HepG2 cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/2/2012
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085586BDBM50085586(5-(4-{2-[1-(5-Phenyl-pyridin-2-yl)-eth-(E)-ylidene...)
Affinity DataEC50:  1.10E+3nMAssay Description:Peroxisome proliferator activated receptor gamma agonistic activity in HepG2 cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/2/2012
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085579BDBM50085579(5-(4-{2-[1-(4-Pyridin-4-yl-phenyl)-eth-(E)-ylidene...)
Affinity DataEC50:  1.60E+3nMAssay Description:Peroxisome proliferator activated receptor gamma agonistic activity in HepG2 cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/2/2012
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085577BDBM50085577(5-(4-{2-[1-Biphenyl-4-yl-prop-(E)-ylideneaminooxy]...)
Affinity DataEC50:  1.60E+3nMAssay Description:Peroxisome proliferator activated receptor gamma agonistic activity in HepG2 cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/2/2012
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085583BDBM50085583(5-(4-{2-[1-Phenyl-eth-(E)-ylideneaminooxy]-ethoxy}...)
Affinity DataEC50:  1.70E+3nMAssay Description:Peroxisome proliferator activated receptor gamma agonistic activity in HepG2 cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/2/2012
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085588BDBM50085588(5-(4-{2-[1-Pyridin-3-yl-eth-(E)-ylideneaminooxy]-e...)
Affinity DataEC50:  2.80E+3nMAssay Description:Peroxisome proliferator activated receptor gamma agonistic activity in HepG2 cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/2/2012
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085590BDBM50085590(5-(4-{2-[1-Pyridin-2-yl-eth-(E)-ylideneaminooxy]-e...)
Affinity DataEC50:  2.80E+3nMAssay Description:Peroxisome proliferator activated receptor gamma agonistic activity in HepG2 cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/2/2012
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50049240BDBM50049240((+-)-5-((4-(2-(5-ethyl-2-pyridinyl)ethoxy)phenyl)m...)
Affinity DataEC50:  7.60E+3nMAssay Description:Peroxisome proliferator activated receptor gamma agonistic activity in HepG2 cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/2/2012
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085585BDBM50085585(5-(4-{2-[1-Pyridin-4-yl-eth-(E)-ylideneaminooxy]-e...)
Affinity DataEC50:  7.90E+3nMAssay Description:Peroxisome proliferator activated receptor gamma agonistic activity in HepG2 cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/2/2012
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085582BDBM50085582(5-(4-{2-[1-Biphenyl-2-yl-eth-(E)-ylideneaminooxy]-...)
Affinity DataEC50: >1.00E+5nMAssay Description:Peroxisome proliferator activated receptor gamma agonistic activity in HepG2 cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/2/2012
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085580BDBM50085580(5-(4-{3-[1-Biphenyl-4-yl-eth-(E)-ylideneaminooxy]-...)
Affinity DataEC50: >1.00E+5nMAssay Description:Peroxisome proliferator activated receptor gamma agonistic activity in HepG2 cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/2/2012
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085578BDBM50085578(5-(4-{2-[1-Biphenyl-4-yl-but-(E)-ylideneaminooxy]-...)
Affinity DataEC50: >1.00E+5nMAssay Description:Peroxisome proliferator activated receptor gamma agonistic activity in HepG2 cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/2/2012
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085589BDBM50085589(Biphenyl-4-carbaldehyde O-{2-[4-(2,4-dioxo-thiazol...)
Affinity DataEC50: >1.00E+5nMAssay Description:Peroxisome proliferator activated receptor gamma agonistic activity in HepG2 cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/2/2012
Entry Details Article
PubMed