Compile Data Set for Download or QSAR
Report error Found 20 of affinity data for UniProtKB/TrEMBL: P13051
TargetUracil-DNA glycosylase(Human)
Johns Hopkins University

LigandPNGBDBM36453(CID25210526 | 6-[3-[(3-Carboxy-benzylidene)aminoox...)
Affinity DataIC50: 1.30E+3nMpH: 8.0Assay Description:Inhibition of human uracil DNA glycosylase using high-throughput fluorescent molecular beacon DNA substrate.More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/4/2011
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetUracil-DNA glycosylase(Human)
Johns Hopkins University

LigandPNGBDBM50078333(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)
Johns Hopkins University

LigandPNGBDBM50078341(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)
Johns Hopkins University

LigandPNGBDBM50078334(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)
Johns Hopkins University

LigandPNGBDBM50078336(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)
Johns Hopkins University

LigandPNGBDBM50078338(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)
Johns Hopkins University

LigandPNGBDBM50078339(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)
Johns Hopkins University

LigandPNGBDBM50078340(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)
Johns Hopkins University

LigandPNGBDBM50078335(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)
Johns Hopkins University

LigandPNGBDBM36452(CID25210531 | 6-[[(3-Carboxy-benzylidene)-aminooxy...)
Affinity DataIC50: 4.00E+4nMpH: 8.0Assay Description:Inhibition of human uracil DNA glycosylase using high-throughput fluorescent molecular beacon DNA substrate.More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/4/2011
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetUracil-DNA glycosylase(Human)
Johns Hopkins University

LigandPNGBDBM50078342(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)
Johns Hopkins University

LigandPNGBDBM50078337(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)
Johns Hopkins University

LigandPNGBDBM36454(CID25210538 | 6-[[3-(3-Carboxybenzyl)aminopropylim...)
Affinity DataIC50: 1.00E+5nMpH: 8.0Assay Description:Inhibition of human uracil DNA glycosylase using high-throughput fluorescent molecular beacon DNA substrate.More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/4/2011
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetUracil-DNA glycosylase(Human)
Johns Hopkins University

LigandPNGBDBM50078343(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)
Johns Hopkins University

LigandPNGBDBM50028333(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)
Johns Hopkins University

LigandPNGBDBM50078344(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)
Johns Hopkins University

LigandPNGBDBM36455(CID25210542 | 6-[4-[(3-Carboxybenzylamino)butylami...)
Affinity DataIC50: 3.15E+5nMpH: 8.0Assay Description:Inhibition of human uracil DNA glycosylase using high-throughput fluorescent molecular beacon DNA substrate.More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/4/2011
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetUracil-DNA glycosylase(Human)
Johns Hopkins University

LigandPNGBDBM50028325(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
TargetUracil-DNA glycosylase(Human)
Johns Hopkins University

LigandPNGBDBM36456(CID25210524 | 6-[3-(Aminooxypropylamino)methyl]ura...)
Affinity DataKi:  7.00E+5nMpH: 8.0Assay Description:Inhibition of human uracil DNA glycosylase using high-throughput fluorescent molecular beacon DNA substrate.More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/4/2011
Entry Details Article
PubMed
TargetUracil-DNA glycosylase(Human)
Johns Hopkins University

LigandPNGBDBM36457(CID25210536 | 3-[(3-Aminopropoxyimino)methyl]uraci...)
Affinity DataKi:  7.50E+5nMpH: 8.0Assay Description:Inhibition of human uracil DNA glycosylase using high-throughput fluorescent molecular beacon DNA substrate.More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/4/2011
Entry Details Article
PubMed