Compile Data Set for Download or QSAR
maximum 50k data
Found 40 with Last Name = 'hunter' and Initial = 'wn'
TargetPteridine reductase(Trypanosoma brucei brucei)
University of Dundee

LigandPNGBDBM31801(2-aminobenzimidazole deriv., 12)
Affinity DataKi:  7nM ΔG°:  -46.2kJ/molepH: 6.0 T: 2°CAssay Description:TbPTR1 activity was measured in 96-well microtiter plates via reduction of cytochrome c (cytc) as a result of the enzymatic production of tetrahydrob...More data for this Ligand-Target Pair
TargetBifunctional methylenetetrahydrofolate dehydrogenase/cyclohydrolase, mitochondrial(Homo sapiens (Human))
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50123588(CHEMBL297258)
Affinity DataKi:  29nMAssay Description:Competitive inhibition of human FolD dehydrogenase activityMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM18050(2-[(4-{[(2,4-diaminopteridin-6-yl)methyl](methyl)a...)
Affinity DataKi:  39nMAssay Description:Inhibition of Leishmania major recombinant PTR1More data for this Ligand-Target Pair
TargetPteridine reductase(Trypanosoma brucei brucei)
University of Dundee

LigandPNGBDBM31800(2-aminobenzimidazole deriv., 11)
Affinity DataKi:  47nM ΔG°:  -41.5kJ/molepH: 6.0 T: 2°CAssay Description:TbPTR1 activity was measured in 96-well microtiter plates via reduction of cytochrome c (cytc) as a result of the enzymatic production of tetrahydrob...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50303504(2,4-diamino-6,7-diisopropylpteridin-1-ium | 6,7-bi...)
Affinity DataKi:  240nMAssay Description:Inhibition of Leishmania major recombinant PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase(Trypanosoma brucei brucei)
University of Dundee

LigandPNGBDBM31798(2-aminobenzimidazole deriv., 9)
Affinity DataKi:  400nM ΔG°:  -36.3kJ/molepH: 6.0 T: 2°CAssay Description:TbPTR1 activity was measured in 96-well microtiter plates via reduction of cytochrome c (cytc) as a result of the enzymatic production of tetrahydrob...More data for this Ligand-Target Pair
TargetPteridine reductase(Trypanosoma brucei brucei)
University of Dundee

LigandPNGBDBM31799(2-aminobenzimidazole deriv., 10)
Affinity DataKi:  510nM ΔG°:  -35.7kJ/molepH: 6.0 T: 2°CAssay Description:TbPTR1 activity was measured in 96-well microtiter plates via reduction of cytochrome c (cytc) as a result of the enzymatic production of tetrahydrob...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50303518(2,4-diamino-6-(benzylthio)pyrimidin-1-ium | 6-(ben...)
Affinity DataKi:  600nMAssay Description:Inhibition of Leishmania major recombinant PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50303514(2-amino-6-(1,3-benzodioxol-5-yl)-4-oxo-4,7-dihydro...)
Affinity DataKi:  2.60E+3nMAssay Description:Inhibition of Leishmania major recombinant PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50303519(6-[(4'-Methoxybenzyl)sulfanyl]-2,4-pyrimidinediami...)
Affinity DataKi:  2.70E+3nMAssay Description:Inhibition of Leishmania major recombinant PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM6644(6‐phenylpteridine‐2,4,7‐triamine...)
Affinity DataKi:  3.40E+3nMAssay Description:Inhibition of Leishmania major recombinant PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50303512(2-amino-6-(4-methoxyphenyl)-4-oxo-4,7-dihydro-3H-p...)
Affinity DataKi:  3.40E+3nMAssay Description:Inhibition of Leishmania major recombinant PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50303513(2-amino-6-(3-formylphenyl)-4-oxo-4,7-dihydro-3H-py...)
Affinity DataKi:  4.20E+3nMAssay Description:Inhibition of Leishmania major recombinant PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase(Trypanosoma brucei brucei)
University of Dundee

LigandPNGBDBM31795(2-aminobenzimidazole deriv., 6)
Affinity DataKi:  9.80E+3nM ΔG°:  -28.4kJ/molepH: 6.0 T: 2°CAssay Description:TbPTR1 activity was measured in 96-well microtiter plates via reduction of cytochrome c (cytc) as a result of the enzymatic production of tetrahydrob...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase(Trypanosoma brucei brucei)
University of Dundee

LigandPNGBDBM31794(2-aminobenzimidazole deriv., 4 | 5-Chloro-1H-benzo...)
Affinity DataKi:  1.06E+4nM ΔG°:  -28.2kJ/molepH: 6.0 T: 2°CAssay Description:TbPTR1 activity was measured in 96-well microtiter plates via reduction of cytochrome c (cytc) as a result of the enzymatic production of tetrahydrob...More data for this Ligand-Target Pair
TargetPteridine reductase 1(Leishmania major)
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50303505(6,7,7-trimethyl-7,8-dihydropteridine-2,4-diamine |...)
Affinity DataKi:  1.20E+4nMAssay Description:Inhibition of Leishmania major recombinant PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50303511(2-amino-6-(4-ethylphenyl)-4-oxo-4,7-dihydro-3H-pyr...)
Affinity DataKi:  1.64E+4nMAssay Description:Inhibition of Leishmania major recombinant PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase(Trypanosoma brucei brucei)
University of Dundee

LigandPNGBDBM31791(2-aminobenzothiazole deriv., 2)
Affinity DataKi:  2.11E+4nM ΔG°:  -26.5kJ/molepH: 6.0 T: 2°CAssay Description:TbPTR1 activity was measured in 96-well microtiter plates via reduction of cytochrome c (cytc) as a result of the enzymatic production of tetrahydrob...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase(Trypanosoma brucei brucei)
University of Dundee

LigandPNGBDBM31797(2-aminobenzimidazole deriv., 8)
Affinity DataKi:  2.39E+4nM ΔG°:  -26.2kJ/molepH: 6.0 T: 2°CAssay Description:TbPTR1 activity was measured in 96-well microtiter plates via reduction of cytochrome c (cytc) as a result of the enzymatic production of tetrahydrob...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50303507(2-amino-4-oxo-4,7-dihydro-3H-pyrrolo[2,3-d]pyrimid...)
Affinity DataKi: >2.70E+4nMAssay Description:Inhibition of Leishmania major recombinant PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50303506(2-amino-3H-pyrrolo[2,3-d]pyrimidine-4(7H)-thione |...)
Affinity DataKi: >2.70E+4nMAssay Description:Inhibition of Leishmania major recombinant PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50028122(2-Amino-3,7-dihydro-pyrrolo[2,3-d]pyrimidin-4-one ...)
Affinity DataKi: >2.70E+4nMAssay Description:Inhibition of Leishmania major recombinant PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50303509(2-amino-6-bromo-4-oxo-4,7-dihydro-3H-pyrrolo[2,3-d...)
Affinity DataKi: >2.70E+4nMAssay Description:Inhibition of Leishmania major recombinant PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50303510(2-amino-4-oxo-6-phenyl-4,7-dihydro-3H-pyrrolo[2,3-...)
Affinity DataKi: >2.70E+4nMAssay Description:Inhibition of Leishmania major recombinant PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50303508(2-amino-5-(2-phenylethyl)-3,7-dihydro-4H-pyrrolo[2...)
Affinity DataKi: >2.70E+4nMAssay Description:Inhibition of Leishmania major recombinant PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50303516(2,4-diamino-6-(cyclopropylamino)pyrimidin-1-ium | ...)
Affinity DataKi: >2.70E+4nMAssay Description:Inhibition of Leishmania major recombinant PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50303517(2,4-diamino-6-(p-tolylthio)pyrimidin-1-ium | 6-[(4...)
Affinity DataKi:  2.70E+4nMAssay Description:Inhibition of Leishmania major recombinant PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50303515(2,4,6-triaminopyrimidin-1-ium | CHEMBL571518 | PYR...)
Affinity DataKi: >2.70E+4nMAssay Description:Inhibition of Leishmania major recombinant PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase(Trypanosoma brucei brucei)
University of Dundee

LigandPNGBDBM31793(2-aminobenzothiazole deriv., 3)
Affinity DataKi:  1.41E+5nM ΔG°:  -21.8kJ/molepH: 6.0 T: 2°CAssay Description:TbPTR1 activity was measured in 96-well microtiter plates via reduction of cytochrome c (cytc) as a result of the enzymatic production of tetrahydrob...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase(Trypanosoma brucei brucei)
University of Dundee

LigandPNGBDBM31796(2-aminobenzimidazole deriv., 7)
Affinity DataKi: >2.00E+5nM ΔG°: >-21.0kJ/molepH: 6.0 T: 2°CAssay Description:TbPTR1 activity was measured in 96-well microtiter plates via reduction of cytochrome c (cytc) as a result of the enzymatic production of tetrahydrob...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase(Trypanosoma brucei brucei)
University of Dundee

LigandPNGBDBM7960(1H-1,3-benzodiazol-2-amine | 2-Aminobenzimidazole ...)
Affinity DataKi:  2.88E+5nM ΔG°:  -20.1kJ/molepH: 6.0 T: 2°CAssay Description:TbPTR1 activity was measured in 96-well microtiter plates via reduction of cytochrome c (cytc) as a result of the enzymatic production of tetrahydrob...More data for this Ligand-Target Pair
Target2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase(Escherichia coli (strain K12))
University of Dundee

LigandPNGBDBM31913(1-beta-D-arabinofuranosylcytosine 5-monophosphate ...)
Affinity DataKd:  1.89E+7nMpH: 7.0 T: 2°CAssay Description:An SPR assay was used to determine the binding affinities of compounds. Experiments were performed on a Biacore 3000 (Biacore, Uppsala, Sweden) instr...More data for this Ligand-Target Pair
Target2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase(Escherichia coli (strain K12))
University of Dundee

LigandPNGBDBM31912(4-(5-amino-1,3,4-oxadiazol-2-yl)-1,2,5-oxadiazol-3...)
Affinity DatapH: 7.0 T: 2°CAssay Description:An SPR assay was used to determine the binding affinities of compounds. Experiments were performed on a Biacore 3000 (Biacore, Uppsala, Sweden) instr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase(Escherichia coli (strain K12))
University of Dundee

LigandPNGBDBM31911(2-[(2,6-diaminopyrimidin-4-yl)sulfanyl]acetamide, ...)
Affinity DatapH: 7.0 T: 2°CAssay Description:An SPR assay was used to determine the binding affinities of compounds. Experiments were performed on a Biacore 3000 (Biacore, Uppsala, Sweden) instr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase(Escherichia coli (strain K12))
University of Dundee

LigandPNGBDBM31916(Tryptophanhydroxamate, 13)
Affinity DataKd:  1.92E+3nMpH: 7.0 T: 2°CAssay Description:An SPR assay was used to determine the binding affinities of compounds. Experiments were performed on a Biacore 3000 (Biacore, Uppsala, Sweden) instr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase(Escherichia coli (strain K12))
University of Dundee

LigandPNGBDBM31909(Cytidine 2,3-cyclic phosphate, 6)
Affinity DataKd:  2.05E+7nMpH: 7.0 T: 2°CAssay Description:An SPR assay was used to determine the binding affinities of compounds. Experiments were performed on a Biacore 3000 (Biacore, Uppsala, Sweden) instr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase(Escherichia coli (strain K12))
University of Dundee

LigandPNGBDBM31907(5-oxopentanoic acid, 4)
Affinity DatapH: 7.0 T: 2°CAssay Description:An SPR assay was used to determine the binding affinities of compounds. Experiments were performed on a Biacore 3000 (Biacore, Uppsala, Sweden) instr...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
Target2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase(Escherichia coli (strain K12))
University of Dundee

LigandPNGBDBM31914(4-amino-1-[(2R,3R,4S,5R)-3, 4-dihydroxy-5-(hydroxy...)
Affinity DataKd:  2.02E+6nMpH: 7.0 T: 2°CAssay Description:An SPR assay was used to determine the binding affinities of compounds. Experiments were performed on a Biacore 3000 (Biacore, Uppsala, Sweden) instr...More data for this Ligand-Target Pair
Target2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase(Escherichia coli (strain K12))
University of Dundee

LigandPNGBDBM31915(CDV | Cidofovir | HPMPC | US10071110, Compound Cid...)
Affinity DataKd:  4.00E+7nMpH: 7.0 T: 2°CAssay Description:An SPR assay was used to determine the binding affinities of compounds. Experiments were performed on a Biacore 3000 (Biacore, Uppsala, Sweden) instr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase(Escherichia coli (strain K12))
University of Dundee

LigandPNGBDBM31910(Cyclic CMP, 7)
Affinity DataKd:  9.00E+5nMpH: 7.0 T: 2°CAssay Description:An SPR assay was used to determine the binding affinities of compounds. Experiments were performed on a Biacore 3000 (Biacore, Uppsala, Sweden) instr...More data for this Ligand-Target Pair