Compile Data Set for Download or QSAR
Report error Found 31 Enz. Inhib. hit(s) with all data for entry = 50020807
TargetPeroxisome proliferator-activated receptor gamma(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50217867BDBM50217867(CHEMBL250278 | CHEMBL248663 | ethyl 1-(methylnitro...)
Affinity DataEC50:  15nMAssay Description:Agonist activity at human PPARgamma expressed in NIH3T3 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50217866BDBM50217866(N-cyclopropyl-1-(methylnitroso)-6-[2-(morpholin-4-...)
Affinity DataEC50:  20nMAssay Description:Agonist activity at human PPARgamma expressed in NIH3T3 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50217858BDBM50217858(propan-2-yl 1-(methylnitroso)-6-[2-(morpholin-4-yl...)
Affinity DataEC50:  25nMAssay Description:Agonist activity at human PPARgamma expressed in NIH3T3 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50217878BDBM50217878(ethyl 1-(methylnitroso)-6-[2-(4-methylpiperazin-1-...)
Affinity DataEC50:  30nMAssay Description:Agonist activity at human PPARgamma expressed in NIH3T3 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50217876BDBM50217876(ethyl 1-(methylnitroso)-3-phenyl-6-[2-(pyridin-2-y...)
Affinity DataEC50:  30nMAssay Description:Agonist activity at human PPARgamma expressed in NIH3T3 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50217867BDBM50217867(CHEMBL250278 | CHEMBL248663 | ethyl 1-(methylnitro...)
Affinity DataEC50:  40nMAssay Description:Agonist activity at human PPARgamma expressed in NIH3T3 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50217853BDBM50217853(ethyl 1-(methylnitroso)-3-phenyl-6-(3-phenylpropox...)
Affinity DataEC50:  50nMAssay Description:Agonist activity at human PPARgamma expressed in NIH3T3 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50217857BDBM50217857(ethyl 3-(furan-3-yl)-1-(methylnitroso)-6-(3-phenyl...)
Affinity DataEC50:  50nMAssay Description:Agonist activity at human PPARgamma expressed in NIH3T3 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50217855BDBM50217855(ethyl 3-(4-chlorophenyl)-1-(methylnitroso)-6-(3-ph...)
Affinity DataEC50:  70nMAssay Description:Agonist activity at human PPARgamma expressed in NIH3T3 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50217871BDBM50217871(ethyl 6-{2-[cyclohexyl(methyl)amino]ethoxy}-1-(met...)
Affinity DataEC50:  70nMAssay Description:Agonist activity at human PPARgamma expressed in NIH3T3 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50217869BDBM50217869(ethyl 1-(methylnitroso)-3-(pentan-3-yl)-6-(3-pheny...)
Affinity DataEC50:  80nMAssay Description:Agonist activity at human PPARgamma expressed in NIH3T3 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50217877BDBM50217877(ethyl 3-ethyl-1-(methylnitroso)-6-(3-phenylpropoxy...)
Affinity DataEC50:  80nMAssay Description:Agonist activity at human PPARgamma expressed in NIH3T3 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50217875BDBM50217875(ethyl 1-(methylnitroso)-3-phenyl-6-(pyridin-2-ylme...)
Affinity DataEC50:  90nMAssay Description:Agonist activity at human PPARgamma expressed in NIH3T3 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50217864BDBM50217864(methyl 1-(methylnitroso)-6-[2-(morpholin-4-yl)etho...)
Affinity DataEC50:  140nMAssay Description:Agonist activity at human PPARgamma expressed in NIH3T3 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50217863BDBM50217863(ethyl 1-(methylnitroso)-3-phenyl-6-(4-phenylbutoxy...)
Affinity DataEC50:  150nMAssay Description:Agonist activity at human PPARgamma expressed in NIH3T3 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50217859BDBM50217859(4-(2-{[1-(methylnitroso)-3-phenyl-1H-inden-6-yl]ox...)
Affinity DataEC50:  150nMAssay Description:Agonist activity at human PPARgamma expressed in NIH3T3 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50217852BDBM50217852(ethyl 1-(methylnitroso)-6-(3-phenylpropoxy)-3-(thi...)
Affinity DataEC50:  190nMAssay Description:Agonist activity at human PPARgamma expressed in NIH3T3 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50217861BDBM50217861(ethyl 1-(methylnitroso)-3-phenyl-6-{[(2E)-3-phenyl...)
Affinity DataEC50:  200nMAssay Description:Agonist activity at human PPARgamma expressed in NIH3T3 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50217865BDBM50217865(ethyl 1-(methylnitroso)-3-phenyl-6-(2-phenylethoxy...)
Affinity DataEC50:  200nMAssay Description:Agonist activity at human PPARgamma expressed in NIH3T3 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50217874BDBM50217874(1-(methylnitroso)-6-[2-(morpholin-4-yl)ethoxy]-3-p...)
Affinity DataEC50:  200nMAssay Description:Agonist activity at human PPARgamma expressed in NIH3T3 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50217868BDBM50217868(ethyl 3-(2H-1,3-benzodioxol-5-yl)-1-(methylnitroso...)
Affinity DataEC50:  250nMAssay Description:Agonist activity at human PPARgamma expressed in NIH3T3 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50217854BDBM50217854(ethyl (1E)-6-methoxy-1-[methyl(oxido)imino]-3-phen...)
Affinity DataEC50:  300nMAssay Description:Agonist activity at human PPARgamma expressed in NIH3T3 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50217860BDBM50217860(ethyl 1-(methylnitroso)-3-(3-methylphenyl)-6-(3-ph...)
Affinity DataEC50:  300nMAssay Description:Agonist activity at human PPARgamma expressed in NIH3T3 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 28681BDBM28681(cid_5281055 | [3H]rosiglitazone | CHEMBL121 | ROSI...)
Affinity DataEC50:  320nMAssay Description:Agonist activity at human PPARgamma expressed in NIH3T3 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50217879BDBM50217879(ethyl 1-(methylnitroso)-3-(4-methylphenyl)-6-(3-ph...)
Affinity DataEC50:  660nMAssay Description:Agonist activity at human PPARgamma expressed in NIH3T3 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50217856BDBM50217856(ethyl 6-[2-(adamantan-1-yl)ethoxy]-1-(methylnitros...)
Affinity DataEC50:  840nMAssay Description:Agonist activity at human PPARgamma expressed in NIH3T3 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50217851BDBM50217851(ethyl 3-(1H-imidazol-2-yl)-1-(methylnitroso)-6-(3-...)
Affinity DataEC50: >1.00E+3nMAssay Description:Agonist activity at human PPARgamma expressed in NIH3T3 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50217872BDBM50217872((E)-ethyl 6-methoxy-1-(methoxyimino)-3-phenyl-1H-i...)
Affinity DataEC50:  1.50E+3nMAssay Description:Agonist activity at human PPARgamma expressed in NIH3T3 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50217862BDBM50217862(ethyl 1-(benzylnitroso)-6-methoxy-3-phenyl-1H-inde...)
Affinity DataEC50: >1.00E+4nMAssay Description:Agonist activity at human PPARgamma expressed in NIH3T3 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50191606BDBM50191606(CHEMBL413047 | CHEMBL250822 | 1-hydroxyimino-6-met...)
Affinity DataEC50: >1.00E+4nMAssay Description:Agonist activity at human PPARgamma expressed in NIH3T3 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50217870BDBM50217870(ethyl (1E)-1-[ethyl(oxido)imino]-6-methoxy-3-pheny...)
Affinity DataEC50: >1.00E+4nMAssay Description:Agonist activity at human PPARgamma expressed in NIH3T3 cells by GAL4 transactivation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed