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Found 18 of ic50 for UniProtKB: P13051
TargetUracil-DNA glycosylase(Homo sapiens (Human))
Johns Hopkins University

LigandPNGBDBM36453(6-[3-[(3-Carboxy-benzylidene)aminooxypropylamino]-...)
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
TargetUracil-DNA glycosylase(Homo sapiens (Human))
Johns Hopkins University

LigandPNGBDBM50078333(6-(4-Octyl-phenylamino)-1H-pyrimidine-2,4-dione | ...)
Affinity DataIC50:  8.00E+3nMAssay Description:Inhibitory potency of the compound against HSV-1 Uracil-DNA glycosylaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUracil-DNA glycosylase(Homo sapiens (Human))
Johns Hopkins University

LigandPNGBDBM50078341(1-(2-Hydroxy-ethyl)-6-(4-octyl-phenylamino)-1H-pyr...)
Affinity DataIC50:  1.00E+4nMAssay Description:Inhibitory potency of the compound against HSV-1 Uracil-DNA glycosylaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUracil-DNA glycosylase(Homo sapiens (Human))
Johns Hopkins University

LigandPNGBDBM50078334(1-(2-Methoxy-ethyl)-6-(4-octyl-phenylamino)-1H-pyr...)
Affinity DataIC50:  1.50E+4nMAssay Description:Inhibitory potency of the compound against HSV-1 Uracil-DNA glycosylaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUracil-DNA glycosylase(Homo sapiens (Human))
Johns Hopkins University

LigandPNGBDBM50078336(6-(4-Hexyl-phenylamino)-1-(2-hydroxy-ethyl)-1H-pyr...)
Affinity DataIC50:  2.00E+4nMAssay Description:Inhibitory potency of the compound against HSV-1 UDG (Herpes Simplex virus type-I Uracil DNA glycosylase)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUracil-DNA glycosylase(Homo sapiens (Human))
Johns Hopkins University

LigandPNGBDBM50078338(6-(4-Octyloxy-phenylamino)-1H-pyrimidine-2,4-dione...)
Affinity DataIC50:  2.50E+4nMAssay Description:Inhibitory potency of the compound against HSV-1 Uracil-DNA glycosylaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUracil-DNA glycosylase(Homo sapiens (Human))
Johns Hopkins University

LigandPNGBDBM50078339(6-(4-Hexyloxy-phenylamino)-1H-pyrimidine-2,4-dione...)
Affinity DataIC50:  3.00E+4nMAssay Description:Inhibitory potency of the compound against HSV-1 UDG (Herpes Simplex virus type-I Uracil DNA glycosylase)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUracil-DNA glycosylase(Homo sapiens (Human))
Johns Hopkins University

LigandPNGBDBM50078340(6-(4-Hexyl-phenylamino)-1H-pyrimidine-2,4-dione | ...)
Affinity DataIC50:  3.00E+4nMAssay Description:Inhibitory potency of the compound against HSV-1 UDG (Herpes Simplex virus type-I Uracil DNA glycosylase)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUracil-DNA glycosylase(Homo sapiens (Human))
Johns Hopkins University

LigandPNGBDBM50078335(6-(4-Decyl-phenylamino)-1H-pyrimidine-2,4-dione | ...)
Affinity DataIC50:  3.50E+4nMAssay Description:Inhibitory potency of the compound against HSV-1 Uracil-DNA glycosylaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUracil-DNA glycosylase(Homo sapiens (Human))
Johns Hopkins University

LigandPNGBDBM36452(6-[[(3-Carboxy-benzylidene)-aminooxy]ethoxyimino]m...)
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
TargetUracil-DNA glycosylase(Homo sapiens (Human))
Johns Hopkins University

LigandPNGBDBM50078342(6-(4-Hexyl-phenylamino)-1-(3-hydroxy-propyl)-1H-py...)
Affinity DataIC50:  9.00E+4nMAssay Description:Inhibitory potency of the compound against HSV-1 UDG (Herpes Simplex virus type-I Uracil DNA glycosylase)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUracil-DNA glycosylase(Homo sapiens (Human))
Johns Hopkins University

LigandPNGBDBM50078337(6-(4-Hexyl-phenylamino)-1-(2-methoxy-ethyl)-1H-pyr...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibitory potency of the compound against HSV-1 UDG (Herpes Simplex virus type-I Uracil DNA glycosylase)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUracil-DNA glycosylase(Homo sapiens (Human))
Johns Hopkins University

LigandPNGBDBM50078343(6-(4-Hexyl-phenylamino)-1-(3-methoxy-propyl)-1H-py...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibitory potency of the compound against HSV-1 UDG (Herpes Simplex virus type-I Uracil DNA glycosylase)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUracil-DNA glycosylase(Homo sapiens (Human))
Johns Hopkins University

LigandPNGBDBM36454(6-[[3-(3-Carboxybenzyl)aminopropylimino]methyl]ura...)
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
Ligand InfoPC cidPC sidPDB
TargetUracil-DNA glycosylase(Homo sapiens (Human))
Johns Hopkins University

LigandPNGBDBM50028333(6-(4-Butyl-phenylamino)-1H-pyrimidine-2,4-dione | ...)
Affinity DataIC50:  1.50E+5nMAssay Description:Inhibitory potency of the compound against HSV-1 UDG (Herpes Simplex virus type-I Uracil DNA glycosylase)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUracil-DNA glycosylase(Homo sapiens (Human))
Johns Hopkins University

LigandPNGBDBM50078344(6-(4-Octyl-phenoxy)-1H-pyrimidine-2,4-dione | CHEM...)
Affinity DataIC50:  1.50E+5nMAssay Description:Inhibitory potency of the compound against HSV-1 Uracil-DNA glycosylaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUracil-DNA glycosylase(Homo sapiens (Human))
Johns Hopkins University

LigandPNGBDBM36455(6-[4-[(3-Carboxybenzylamino)butylamino]methyl]urac...)
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
TargetUracil-DNA glycosylase(Homo sapiens (Human))
Johns Hopkins University

LigandPNGBDBM50028325(6-(4-Ethyl-phenylamino)-1H-pyrimidine-2,4-dione | ...)
Affinity DataIC50:  5.00E+5nMAssay Description:Inhibitory potency of the compound against HSV-1 UDG (Herpes Simplex virus type-I Uracil DNA glycosylase)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed