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Found 830 with Last Name = 'nguyen' and Initial = 'c'
Target5-hydroxytryptamine receptor 4(Homo sapiens (Human))
Drug Discovery Laboratory

Curated by ChEMBL
LigandPNGBDBM29525(3H-GR113808 | CHEMBL518682 | GR 113808 | [3H] GR 1...)
Affinity DataKi:  0.0398nMAssay Description:Displacement of [3H]GR113808 from human 5-HT4B receptor expressed in HEK293 cells after 1 hr by liquid scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 4(Homo sapiens (Human))
Drug Discovery Laboratory

Curated by ChEMBL
LigandPNGBDBM85026(N-(1-Butylpiperidine-4-ylmethyl)-1,2-(trimethylene...)
Affinity DataKi:  0.100nMAssay Description:Displacement of [3H]GR113808 from human 5-HT4B receptor expressed in HEK293 cells after 1 hr by liquid scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 4(Homo sapiens (Human))
Drug Discovery Laboratory

Curated by ChEMBL
LigandPNGBDBM50492064(CHEMBL2391994)
Affinity DataKi:  0.126nMAssay Description:Displacement of [3H]GR113808 from human 5-HT4B receptor expressed in HEK293 cells after 1 hr by liquid scintillation counting analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetBeta-secretase 1(Homo sapiens (Human))
University Of Illinois At Chicago

LigandPNGBDBM16047((4S)-4-[(2S)-2-[(2R,4S,5S)-5-[(2S)-2-[(2S)-2-[(4S)...)
Affinity DataKi:  1.60nM ΔG°:  -52.2kJ/molepH: 4.5 T: 2°CAssay Description:Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...More data for this Ligand-Target Pair
TargetBeta-secretase 1(Homo sapiens (Human))
University Of Illinois At Chicago

LigandPNGBDBM16250(CHEMBL290001 | N-(tert-butoxycarbonyl)-L-valyl-N-[...)
Affinity DataKi:  2.5nM ΔG°:  -51.1kJ/molepH: 4.5 T: 2°CAssay Description:Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-secretase 1(Homo sapiens (Human))
University Of Illinois At Chicago

LigandPNGBDBM16777(Substrate-based BACE-1 inhibitor, 16 | tert-butyl ...)
Affinity DataKi:  5.90nM ΔG°:  -48.9kJ/molepH: 4.5 T: 2°CAssay Description:Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-secretase 1(Homo sapiens (Human))
University Of Illinois At Chicago

LigandPNGBDBM16781(Substrate-based BACE-1 inhibitor, 23 | tert-butyl ...)
Affinity DataKi:  8nM ΔG°:  -48.1kJ/molepH: 4.5 T: 2°CAssay Description:Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-secretase 1(Homo sapiens (Human))
University Of Illinois At Chicago

LigandPNGBDBM16779(Substrate-based BACE-1 inhibitor, 18 | tert-butyl ...)
Affinity DataKi:  9.40nM ΔG°:  -47.7kJ/molepH: 4.5 T: 2°CAssay Description:Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-secretase 1(Homo sapiens (Human))
University Of Illinois At Chicago

LigandPNGBDBM16772((4S)-4-[(2S)-2-[(2R,4S,5S)-5-[(2S)-2-[(2S)-2-amino...)
Affinity DataKi:  36nM ΔG°:  -44.2kJ/molepH: 4.5 T: 2°CAssay Description:Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-secretase 1(Homo sapiens (Human))
University Of Illinois At Chicago

LigandPNGBDBM16778(Substrate-based BACE-1 inhibitor, 17 | tert-butyl ...)
Affinity DataKi:  50.1nM ΔG°:  -43.3kJ/molepH: 4.5 T: 2°CAssay Description:Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-secretase 1(Homo sapiens (Human))
University Of Illinois At Chicago

LigandPNGBDBM16776(Substrate-based BACE-1 inhibitor, 15 | tert-butyl ...)
Affinity DataKi:  61.4nM ΔG°:  -42.8kJ/molepH: 4.5 T: 2°CAssay Description:Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50064657(CHEMBL277390 | Cyclo(Lys(alphaH2+)-Pro-Aba-[CH2SMe...)
Affinity DataKi:  85nMAssay Description:Inhibitory activity against hydrolysis of Gly-Pro-pNa by CD26 (dipeptidylpeptidase 4) purified from CEM H01 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50190543(1-((2R,4S,5R)-4-hydroxy-5-((tritylamino)methyl)-te...)
Affinity DataKi:  200nMAssay Description:Inhibition of Plasmodium falciparum dUTPaseMore data for this Ligand-Target Pair
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50190556(1-(3-tritylaminopropyl)uracil | CHEMBL211905)
Affinity DataKi:  200nMAssay Description:Inhibition of Plasmodium falciparum dUTPaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50173577(1-{4-Hydroxy-5-[(trityl-amino)-methyl]-tetrahydro-...)
Affinity DataKi:  200nMAssay Description:Inhibitory constant against Plasmodium falciparum deoxyuridine 5'-triphosphate nucleotidohydrolase expressed in Escherichia coli BL21 (DE3) cellsMore data for this Ligand-Target Pair
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50190549(1-[4-hydroxy-3-(tritylaminomethyl)butyl]uracil | C...)
Affinity DataKi:  240nMAssay Description:Inhibition of Plasmodium falciparum dUTPaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50064657(CHEMBL277390 | Cyclo(Lys(alphaH2+)-Pro-Aba-[CH2SMe...)
Affinity DataKi:  470nMAssay Description:Inhibitory kinetic constant against Dipeptidyl peptidase IV purified from CD26-negative C8166 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50190552(1-[(E)-4-trityloxy-2-butenyl]uracil | CHEMBL209610)
Affinity DataKi:  600nMAssay Description:Inhibition of Plasmodium falciparum dUTPaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50190553(1-[2-(trityloxy)ethoxymethyl]uracil | CHEMBL424704...)
Affinity DataKi:  700nMAssay Description:Inhibition of Plasmodium falciparum dUTPaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50190532(1-[4-hydroxy-2-(trityloxymethyl)butyl]uracil | CHE...)
Affinity DataKi:  900nMAssay Description:Inhibition of Plasmodium falciparum dUTPaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50190555(1-(4-tritylaminobutyl)uracil | CHEMBL211181)
Affinity DataKi:  900nMAssay Description:Inhibition of Plasmodium falciparum dUTPaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-secretase 1(Homo sapiens (Human))
University Of Illinois At Chicago

LigandPNGBDBM16775(CHEMBL273916 | Substrate-based BACE-1 inhibitor, 1...)
Affinity DataKi:  1.13E+3nM ΔG°:  -35.3kJ/molepH: 4.5 T: 2°CAssay Description:Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50173540(1-[5-(tert-Butyl-diphenyl-silanyloxymethyl)-2,5-di...)
Affinity DataKi:  1.16E+3nM ΔG°:  -33.9kJ/molepH: 8.0 T: 2°CAssay Description:Nucleotide hydrolysis was monitored by mixing enzyme and substrate with a rapid kinetic accessory (Hi-Tech Scientific) attached to a spectrophotomete...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50190531(1-[(Z)-4-trityloxy-2-butenyl]uracil | CHEMBL377199)
Affinity DataKi:  1.20E+3nMAssay Description:Inhibition of Plasmodium falciparum dUTPaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50173540(1-[5-(tert-Butyl-diphenyl-silanyloxymethyl)-2,5-di...)
Affinity DataKi:  1.20E+3nMAssay Description:Inhibitory constant against Plasmodium falciparum deoxyuridine 5'-triphosphate nucleotidohydrolase expressed in Escherichia coli BL21 (DE3) cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50173535(1-(5-Triphenylsilanyloxymethyl-2,5-dihydro-furan-2...)
Affinity DataKi:  1.30E+3nMAssay Description:Inhibitory constant against Plasmodium falciparum deoxyuridine 5'-triphosphate nucleotidohydrolase expressed in Escherichia coli BL21 (DE3) cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50190564(1-[4-acetyloxy-3-(tritylaminomethyl)butyl]uracil |...)
Affinity DataKi:  1.30E+3nMAssay Description:Inhibition of Plasmodium falciparum dUTPaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial(Homo sapiens (Human))
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50190556(1-(3-tritylaminopropyl)uracil | CHEMBL211905)
Affinity DataKi:  1.40E+3nMAssay Description:Inhibition of human recombinant dUTPaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial(Homo sapiens (Human))
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50190556(1-(3-tritylaminopropyl)uracil | CHEMBL211905)
Affinity DataKi:  1.40E+3nMAssay Description:Inhibition of human dUTPase using dUTP as substrate by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50190547(1-(3-triphenylsilyloxypropyl)uracil | CHEMBL211906)
Affinity DataKi:  1.60E+3nMAssay Description:Inhibition of Plasmodium falciparum dUTPaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50190530(1-(4-trityloxybutyl)uracil | CHEMBL211067)
Affinity DataKi:  1.60E+3nMAssay Description:Inhibition of Plasmodium falciparum dUTPaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50190562(1-(6-triphenylsilyloxyhexyl)uracil | CHEMBL212690)
Affinity DataKi:  1.70E+3nMAssay Description:Inhibition of Plasmodium falciparum dUTPaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50190568(1-(6-(tritylamino)hexyl)pyrimidine-2,4(1H,3H)-dion...)
Affinity DataKi:  1.80E+3nMAssay Description:Inhibition of Plasmodium falciparum dUTPaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50173539(1-(4-Hydroxy-5-trityloxymethyl-tetrahydro-furan-2-...)
Affinity DataKi:  1.80E+3nMAssay Description:Inhibition of Plasmodium falciparum dUTPaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50173539(1-(4-Hydroxy-5-trityloxymethyl-tetrahydro-furan-2-...)
Affinity DataKi:  1.80E+3nMAssay Description:Inhibitory constant against Plasmodium falciparum deoxyuridine 5'-triphosphate nucleotidohydrolase expressed in Escherichia coli BL21 (DE3) cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50173546(1-(5-Trityloxymethyl-2,5-dihydro-furan-2-yl)-1H-py...)
Affinity DataKi:  1.90E+3nM ΔG°:  -32.7kJ/molepH: 8.0 T: 2°CAssay Description:Nucleotide hydrolysis was monitored by mixing enzyme and substrate with a rapid kinetic accessory (Hi-Tech Scientific) attached to a spectrophotomete...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50173546(1-(5-Trityloxymethyl-2,5-dihydro-furan-2-yl)-1H-py...)
Affinity DataKi:  1.90E+3nMAssay Description:Inhibitory constant against Plasmodium falciparum deoxyuridine 5'-triphosphate nucleotidohydrolase expressed in Escherichia coli BL21 (DE3) cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50190550(1-(5-trityloxypentyl)uracil | CHEMBL377472)
Affinity DataKi:  2.00E+3nMAssay Description:Inhibition of Plasmodium falciparum dUTPaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50190565(1-[2-(hydroxymethyl)-4-(trityloxy)butyl]uracil | C...)
Affinity DataKi:  2.20E+3nMAssay Description:Inhibition of Plasmodium falciparum dUTPaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50190567(1-(4-triphenylsilyloxybutyl)uracil | CHEMBL387177)
Affinity DataKi:  2.20E+3nMAssay Description:Inhibition of Plasmodium falciparum dUTPaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50190558(1-(6-trityloxyhexyl)uracil | CHEMBL378414)
Affinity DataKi:  2.30E+3nMAssay Description:Inhibition of Plasmodium falciparum dUTPaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50190533(1-[4-(tert-butoxycarbonylamino)-3-(trityloxymethyl...)
Affinity DataKi:  2.50E+3nMAssay Description:Inhibition of Plasmodium falciparum dUTPaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50190545(1-((2R,4S,5R)-4-hydroxy-5-((triphenylsilyloxy)meth...)
Affinity DataKi:  2.80E+3nMAssay Description:Inhibitory constant against Plasmodium falciparum deoxyuridine 5'-triphosphate nucleotidohydrolase expressed in Escherichia coli BL21 (DE3) cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50190545(1-((2R,4S,5R)-4-hydroxy-5-((triphenylsilyloxy)meth...)
Affinity DataKi:  2.80E+3nMAssay Description:Inhibition of Plasmodium falciparum dUTPaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50173531(1-(4-Hydroxy-5-triphenylsilanyloxymethyl-tetrahydr...)
Affinity DataKi:  2.80E+3nM ΔG°:  -31.7kJ/molepH: 8.0 T: 2°CAssay Description:Nucleotide hydrolysis was monitored by mixing enzyme and substrate with a rapid kinetic accessory (Hi-Tech Scientific) attached to a spectrophotomete...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-secretase 1(Homo sapiens (Human))
University Of Illinois At Chicago

LigandPNGBDBM16774(Substrate-based BACE-1 inhibitor, 13 | tert-butyl ...)
Affinity DataKi:  3.13E+3nM ΔG°:  -32.7kJ/molepH: 4.5 T: 2°CAssay Description:Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50190537(1-(5-triphenylsilyloxypentyl)uracil | CHEMBL212175)
Affinity DataKi:  3.80E+3nMAssay Description:Inhibition of Plasmodium falciparum dUTPaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50266744(1-((2R,4S,5R)-5-((tert-butyldiphenylsilyloxy)methy...)
Affinity DataKi:  4.20E+3nMAssay Description:Inhibitory constant against Plasmodium falciparum deoxyuridine 5'-triphosphate nucleotidohydrolase expressed in Escherichia coli BL21 (DE3) cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50173530(1-[5-(tert-Butyl-diphenyl-silanyloxymethyl)-4-hydr...)
Affinity DataKi:  4.20E+3nM ΔG°:  -30.7kJ/molepH: 8.0 T: 2°CAssay Description:Nucleotide hydrolysis was monitored by mixing enzyme and substrate with a rapid kinetic accessory (Hi-Tech Scientific) attached to a spectrophotomete...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase(Plasmodium falciparum)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50190557(1-(5-(tritylamino)pentyl)pyrimidine-2,4(1H,3H)-dio...)
Affinity DataKi:  4.30E+3nMAssay Description:Inhibition of Plasmodium falciparum dUTPaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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