Compile Data Set for Download or QSAR
Report error Found 35 Enz. Inhib. hit(s) with all data for entry = 6530
TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 136527BDBM136527(US8865714, 14)
Affinity DataIC50: 32nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 136525BDBM136525(US8865714, 12)
Affinity DataIC50: 37nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 136523BDBM136523(US8865714, 10)
Affinity DataIC50: 40nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 136519BDBM136519(US8865714, 6)
Affinity DataIC50: 43nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 136524BDBM136524(US8865714, 11)
Affinity DataIC50: 46nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 136517BDBM136517(US8865714, 4)
Affinity DataIC50: 54nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 136514BDBM136514(US8865714, 1)
Affinity DataIC50: 58nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 136529BDBM136529(US8865714, 16)
Affinity DataIC50: 59nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 136530BDBM136530(US8865714, 17)
Affinity DataIC50: 60nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 136528BDBM136528(US8865714, 15)
Affinity DataIC50: 60nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 136521BDBM136521(US8865714, 8)
Affinity DataIC50: 62nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 136518BDBM136518(US8865714, 5)
Affinity DataIC50: 67nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 136520BDBM136520(US8865714, 7)
Affinity DataIC50: 71nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 136516BDBM136516(US8865714, 3)
Affinity DataIC50: 76nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 136522BDBM136522(US8865714, 9)
Affinity DataIC50: 85nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 136515BDBM136515(US8865714, 2)
Affinity DataIC50: 86nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 136526BDBM136526(US8865714, 13)
Affinity DataIC50: 91nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 124939BDBM124939(US8765750, Reference Example 12)
Affinity DataIC50: 106nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 124943BDBM124943(US8765750, Reference Example 16)
Affinity DataIC50: 204nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 124940BDBM124940(US8765750, Reference Example 13)
Affinity DataIC50: 222nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 124941BDBM124941(US8765750, Reference Example 14)
Affinity DataIC50: 260nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 124942BDBM124942(US8765750, Reference Example 15)
Affinity DataIC50: 318nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 136534BDBM136534(US8865714, Reference Example 4)
Affinity DataIC50: 340nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 136541BDBM136541(US8865714, Reference Example 11)
Affinity DataIC50: 437nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 136535BDBM136535(US8865714, Reference Example 5)
Affinity DataIC50: 732nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 136531BDBM136531(US8865714, Reference Example 1)
Affinity DataIC50: 1.00E+3nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 136532BDBM136532(US8865714, Reference Example 2)
Affinity DataIC50: 1.00E+3nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 136543BDBM136543(US8865714, Reference Example 18)
Affinity DataIC50: 1.00E+3nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 136533BDBM136533(US8865714, Reference Example 3)
Affinity DataIC50: 1.00E+3nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 136542BDBM136542(US8865714, Reference Example 12)
Affinity DataIC50: 1.00E+3nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 136538BDBM136538(US8865714, Reference Example 8)
Affinity DataIC50: 1.00E+3nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 136539BDBM136539(US8865714, Reference Example 9)
Affinity DataIC50: 1.00E+3nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 136540BDBM136540(US8865714, Reference Example 10)
Affinity DataIC50: 1.00E+3nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 136536BDBM136536(US8865714, Reference Example 6)
Affinity DataIC50: 1.00E+3nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent

TargetHematopoietic prostaglandin D synthase(Human)
Taiho Pharmaceutical

US Patent
LigandChemical structure of BindingDB Monomer ID 136537BDBM136537(US8865714, Reference Example 7)
Affinity DataIC50: 1.00E+3nMpH: 8.0 T: 2°CAssay Description:The test was carried out according to the method of Urade, Y. et al. (J. Biol. Chem., 262, 3820-3825, (1987)). More specifically, the reaction mixtur...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2015
Entry Details
US Patent