Compile Data Set for Download or QSAR
Report error Found 14 Enz. Inhib. hit(s) with all data for entry = 50008899
TargetUracil-DNA glycosylase(Human)
University of Massachusetts Medical Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50078333BDBM50078333(6-(4-Octyl-phenylamino)-1H-pyrimidine-2,4-dione | ...)
Affinity DataIC50: 8.00E+3nMAssay Description:Inhibitory potency against HSV-1 Uracil-DNA glycosylaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUracil-DNA glycosylase(Human)
University of Massachusetts Medical Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50078341BDBM50078341(1-(2-Hydroxy-ethyl)-6-(4-octyl-phenylamino)-1H-pyr...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory potency against HSV-1 Uracil-DNA glycosylaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUracil-DNA glycosylase(Human)
University of Massachusetts Medical Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50078334BDBM50078334(1-(2-Methoxy-ethyl)-6-(4-octyl-phenylamino)-1H-pyr...)
Affinity DataIC50: 1.50E+4nMAssay Description:Inhibitory potency against HSV-1 Uracil-DNA glycosylaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUracil-DNA glycosylase(Human)
University of Massachusetts Medical Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50078336BDBM50078336(6-(4-Hexyl-phenylamino)-1-(2-hydroxy-ethyl)-1H-pyr...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibitory potency against HSV-1 UDG (Herpes Simplex virus type-I Uracil DNA glycosylase)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUracil-DNA glycosylase(Human)
University of Massachusetts Medical Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50078338BDBM50078338(6-(4-Octyloxy-phenylamino)-1H-pyrimidine-2,4-dione...)
Affinity DataIC50: 2.50E+4nMAssay Description:Inhibitory potency against HSV-1 Uracil-DNA glycosylaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUracil-DNA glycosylase(Human)
University of Massachusetts Medical Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50078340BDBM50078340(6-(4-Hexyl-phenylamino)-1H-pyrimidine-2,4-dione | ...)
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibitory potency against HSV-1 UDG (Herpes Simplex virus type-I Uracil DNA glycosylase)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUracil-DNA glycosylase(Human)
University of Massachusetts Medical Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50078339BDBM50078339(6-(4-Hexyloxy-phenylamino)-1H-pyrimidine-2,4-dione...)
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibitory potency against HSV-1 UDG (Herpes Simplex virus type-I Uracil DNA glycosylase)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUracil-DNA glycosylase(Human)
University of Massachusetts Medical Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50078335BDBM50078335(6-(4-Decyl-phenylamino)-1H-pyrimidine-2,4-dione | ...)
Affinity DataIC50: 3.50E+4nMAssay Description:Inhibitory potency against HSV-1 Uracil-DNA glycosylaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUracil-DNA glycosylase(Human)
University of Massachusetts Medical Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50078342BDBM50078342(6-(4-Hexyl-phenylamino)-1-(3-hydroxy-propyl)-1H-py...)
Affinity DataIC50: 9.00E+4nMAssay Description:Inhibitory potency against HSV-1 UDG (Herpes Simplex virus type-I Uracil DNA glycosylase)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUracil-DNA glycosylase(Human)
University of Massachusetts Medical Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50078343BDBM50078343(6-(4-Hexyl-phenylamino)-1-(3-methoxy-propyl)-1H-py...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory potency against HSV-1 UDG (Herpes Simplex virus type-I Uracil DNA glycosylase)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUracil-DNA glycosylase(Human)
University of Massachusetts Medical Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50078337BDBM50078337(6-(4-Hexyl-phenylamino)-1-(2-methoxy-ethyl)-1H-pyr...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory potency against HSV-1 UDG (Herpes Simplex virus type-I Uracil DNA glycosylase)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUracil-DNA glycosylase(Human)
University of Massachusetts Medical Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50028333BDBM50028333(6-(4-Butyl-phenylamino)-1H-pyrimidine-2,4-dione | ...)
Affinity DataIC50: 1.50E+5nMAssay Description:Inhibitory potency against HSV-1 UDG (Herpes Simplex virus type-I Uracil DNA glycosylase)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUracil-DNA glycosylase(Human)
University of Massachusetts Medical Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50078344BDBM50078344(6-(4-Octyl-phenoxy)-1H-pyrimidine-2,4-dione | CHEM...)
Affinity DataIC50: 1.50E+5nMAssay Description:Inhibitory potency against HSV-1 Uracil-DNA glycosylaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUracil-DNA glycosylase(Human)
University of Massachusetts Medical Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50028325BDBM50028325(6-(4-Ethyl-phenylamino)-1H-pyrimidine-2,4-dione | ...)
Affinity DataIC50: 5.00E+5nMAssay Description:Inhibitory potency against HSV-1 UDG (Herpes Simplex virus type-I Uracil DNA glycosylase)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed