TargetAldo-keto reductase family 1 member B1(Rattus norvegicus)
Institute Of Oriental Medicine
Curated by ChEMBL
Institute Of Oriental Medicine
Curated by ChEMBL
Affinity DataIC50: 70nMAssay Description:Inhibition of rat lens aldose reductaseMore data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member B1(Rattus norvegicus)
Institute Of Oriental Medicine
Curated by ChEMBL
Institute Of Oriental Medicine
Curated by ChEMBL
Affinity DataIC50: 160nMAssay Description:Inhibition of rat lens aldose reductaseMore data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member B1(Rattus norvegicus)
Institute Of Oriental Medicine
Curated by ChEMBL
Institute Of Oriental Medicine
Curated by ChEMBL
Affinity DataIC50: 1.28E+3nMAssay Description:Inhibition of rat lens aldose reductaseMore data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member B1(Rattus norvegicus)
Institute Of Oriental Medicine
Curated by ChEMBL
Institute Of Oriental Medicine
Curated by ChEMBL
Affinity DataIC50: 1.33E+3nMAssay Description:Inhibition of rat lens aldose reductaseMore data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member B1(Rattus norvegicus)
Institute Of Oriental Medicine
Curated by ChEMBL
Institute Of Oriental Medicine
Curated by ChEMBL
Affinity DataIC50: 1.54E+3nMAssay Description:Inhibition of rat lens aldose reductaseMore data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member B1(Rattus norvegicus)
Institute Of Oriental Medicine
Curated by ChEMBL
Institute Of Oriental Medicine
Curated by ChEMBL
Affinity DataIC50: 5.09E+3nMAssay Description:Inhibition of rat lens aldose reductaseMore data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member B1(Rattus norvegicus)
Institute Of Oriental Medicine
Curated by ChEMBL
Institute Of Oriental Medicine
Curated by ChEMBL
Affinity DataIC50: 6.67E+3nMAssay Description:Inhibition of rat lens aldose reductaseMore data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member B1(Rattus norvegicus)
Institute Of Oriental Medicine
Curated by ChEMBL
Institute Of Oriental Medicine
Curated by ChEMBL
Affinity DataIC50: 7.21E+3nMAssay Description:Inhibition of rat lens aldose reductaseMore data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member B1(Rattus norvegicus)
Institute Of Oriental Medicine
Curated by ChEMBL
Institute Of Oriental Medicine
Curated by ChEMBL
Affinity DataIC50: 9.02E+3nMAssay Description:Inhibition of rat lens aldose reductaseMore data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member B1(Rattus norvegicus)
Institute Of Oriental Medicine
Curated by ChEMBL
Institute Of Oriental Medicine
Curated by ChEMBL
Affinity DataIC50: 4.69E+4nMAssay Description:Inhibition of rat lens aldose reductaseMore data for this Ligand-Target Pair
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Korea University
Curated by ChEMBL
Korea University
Curated by ChEMBL
Affinity DataEC50: 440nMAssay Description:Agonist activity at human recombinant PPARgamma expressed in CHO cells cotransfected with pGL3-PPRE3-TK-luc reporter assessed as beta-galactosidase a...More data for this Ligand-Target Pair
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Korea University
Curated by ChEMBL
Korea University
Curated by ChEMBL
Affinity DataEC50: 1.15E+3nMAssay Description:Agonist activity at human recombinant PPARgamma expressed in CHO cells cotransfected with pGL3-PPRE3-TK-luc reporter assessed as beta-galactosidase a...More data for this Ligand-Target Pair
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Korea University
Curated by ChEMBL
Korea University
Curated by ChEMBL
Affinity DataEC50: 1.11E+4nMAssay Description:Agonist activity at human recombinant PPARgamma expressed in CHO cells cotransfected with pGL3-PPRE3-TK-luc reporter assessed as beta-galactosidase a...More data for this Ligand-Target Pair
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Korea University
Curated by ChEMBL
Korea University
Curated by ChEMBL
Affinity DataEC50: 1.88E+3nMAssay Description:Agonist activity at human PPARgamma expressed in CHO cells co-transfected with pGL3-PPRE3-TK-luc assessed as transactivation after 24 hrs by firefly ...More data for this Ligand-Target Pair
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Korea University
Curated by ChEMBL
Korea University
Curated by ChEMBL
Affinity DataEC50: 440nMAssay Description:Agonist activity at human PPARgamma expressed in CHO cells co-transfected with pGL3-PPRE3-TK-luc assessed as transactivation after 24 hrs by firefly ...More data for this Ligand-Target Pair