Compile Data Set for Download or QSAR
Report error Found 65 Enz. Inhib. hit(s) with all data for entry = 6299
TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120985BDBM120985(US8716285, 42)
Affinity DataIC50: 160nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120989BDBM120989(US8716285, 46)
Affinity DataIC50: 190nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120987BDBM120987(US8716285, 44)
Affinity DataIC50: 210nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120955BDBM120955(US8716285, 12)
Affinity DataIC50: 260nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120952BDBM120952(US8716285, 9)
Affinity DataIC50: 290nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120958BDBM120958(US8716285, 15)
Affinity DataIC50: 300nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120951BDBM120951(US8716285, 8)
Affinity DataIC50: 300nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120974BDBM120974(US8716285, 31)
Affinity DataIC50: 320nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120983BDBM120983(US8716285, 40)
Affinity DataIC50: 350nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120991BDBM120991(US8716285, 48)
Affinity DataIC50: 370nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120986BDBM120986(US8716285, 43)
Affinity DataIC50: 370nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120988BDBM120988(US8716285, 45)
Affinity DataIC50: 390nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120990BDBM120990(US8716285, 47)
Affinity DataIC50: 470nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120996BDBM120996(US8716285, 53)
Affinity DataIC50: 470nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120977BDBM120977(US8716285, 34)
Affinity DataIC50: 480nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120968BDBM120968(US8716285, 25)
Affinity DataIC50: 480nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120973BDBM120973(US8716285, 30)
Affinity DataIC50: 510nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120970BDBM120970(US8716285, 27)
Affinity DataIC50: 520nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120969BDBM120969(US8716285, 26)
Affinity DataIC50: 520nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120945BDBM120945(US8716285, 2)
Affinity DataIC50: 680nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120967BDBM120967(US8716285, 24)
Affinity DataIC50: 720nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120950BDBM120950(US8716285, 7)
Affinity DataIC50: 730nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 121008BDBM121008(US8716285, 65)
Affinity DataIC50: 750nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120959BDBM120959(US8716285, 16)
Affinity DataIC50: 800nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120954BDBM120954(US8716285, 11)
Affinity DataIC50: 800nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 121009BDBM121009(US8716285, 66)
Affinity DataIC50: 830nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120984BDBM120984(US8716285, 41)
Affinity DataIC50: 850nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120972BDBM120972(US8716285, 29)
Affinity DataIC50: 900nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120982BDBM120982(US8716285, 39)
Affinity DataIC50: 910nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120995BDBM120995(US8716285, 52)
Affinity DataIC50: 930nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120949BDBM120949(US8716285, 6)
Affinity DataIC50: 930nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 121004BDBM121004(US8716285, 61)
Affinity DataIC50: 970nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120980BDBM120980(US8716285, 37)
Affinity DataIC50: 990nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120971BDBM120971(US8716285, 28)
Affinity DataIC50: 1.00E+3nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120960BDBM120960(US8716285, 17)
Affinity DataIC50: 1.10E+3nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 121005BDBM121005(US8716285, 62)
Affinity DataIC50: 1.14E+3nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 121007BDBM121007(US8716285, 64)
Affinity DataIC50: 1.22E+3nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120961BDBM120961(US8716285, 18)
Affinity DataIC50: 1.23E+3nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120981BDBM120981(US8716285, 38)
Affinity DataIC50: 1.27E+3nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120994BDBM120994(US8716285, 51)
Affinity DataIC50: 1.28E+3nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120966BDBM120966(US8716285, 23)
Affinity DataIC50: 1.44E+3nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 121003BDBM121003(US8716285, 60)
Affinity DataIC50: 1.46E+3nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120975BDBM120975(US8716285, 32)
Affinity DataIC50: 1.50E+3nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120993BDBM120993(US8716285, 50)
Affinity DataIC50: 1.51E+3nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120963BDBM120963(US8716285, 20)
Affinity DataIC50: 1.52E+3nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 121006BDBM121006(US8716285, 63)
Affinity DataIC50: 1.61E+3nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120957BDBM120957(US8716285, 14)
Affinity DataIC50: 1.66E+3nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120962BDBM120962(US8716285, 19)
Affinity DataIC50: 1.69E+3nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120978BDBM120978(US8716285, 35)
Affinity DataIC50: 1.78E+3nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetHistone deacetylase 8(Human)
Hoffmann-La Roche

US Patent
LigandChemical structure of BindingDB Monomer ID 120953BDBM120953(US8716285, 10)
Affinity DataIC50: 2.13E+3nMAssay Description:Compounds were tested for their ability to inhibit histone deacetylase 8 using an in vitro deacetylation assay. In a detailed procedure, 8 μl o...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

Displayed 1 to 50 (of 65 total ) | Next | Last >>
Jump to: