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Found 18 with Last Name = 'sanejouand' and Initial = 'yh'
TargetPhosphotransferase(Trypanosoma brucei)
Universite Paul Sabatier

LigandPNGBDBM43835(Glucosamine derivative, 8 | MLS000582359 | N-cyclo...)
Affinity DataKi:  2.80E+3nM ΔG°:  -31.7kJ/mole IC50:  5.00E+5nMT: 2°CAssay Description:Competitive inhibition assay for glucosamine derivatives on hexokinase from trypanosoma brucei. The inhibition of hexokinase by compounds was measur...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphotransferase(Trypanosoma brucei)
Universite Paul Sabatier

LigandPNGBDBM43833(2-hydroxy-N''''-(3-keto-5,5-dimethyl-cyclohexen-1-...)
Affinity DataKi:  8.00E+3nM ΔG°:  -29.1kJ/mole IC50:  2.00E+6nMT: 2°CAssay Description:Competitive inhibition assay for glucosamine derivatives on hexokinase from trypanosoma brucei. The inhibition of hexokinase by compounds was measur...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphotransferase(Trypanosoma brucei)
Universite Paul Sabatier

LigandPNGBDBM43832(2-phenylcyclopropane-1,1-dicarboxylic acid diethyl...)
Affinity DataKi:  1.90E+4nM ΔG°:  -26.9kJ/mole IC50:  4.00E+5nMT: 2°CAssay Description:Competitive inhibition assay for glucosamine derivatives on hexokinase from trypanosoma brucei. The inhibition of hexokinase by compounds was measur...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphotransferase(Trypanosoma brucei)
Universite Paul Sabatier

LigandPNGBDBM43834(2-methoxy-4-[[4-(4-methylphenyl)-1-piperazinyl]met...)
Affinity DataKi:  2.50E+4nM ΔG°:  -26.3kJ/mole IC50:  3.00E+6nMT: 2°CAssay Description:Competitive inhibition assay for glucosamine derivatives on hexokinase from trypanosoma brucei. The inhibition of hexokinase by compounds was measur...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphotransferase(Trypanosoma brucei)
Universite Paul Sabatier

LigandPNGBDBM43838(4-O-[5-bromo-2-cyclopropyl-3-(4-methoxyphenyl)-7-m...)
Affinity DataKi:  3.00E+4nM ΔG°:  -25.8kJ/mole IC50:  3.00E+6nMT: 2°CAssay Description:Competitive inhibition assay for glucosamine derivatives on hexokinase from trypanosoma brucei. The inhibition of hexokinase by compounds was measur...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphotransferase(Trypanosoma brucei)
Universite Paul Sabatier

LigandPNGBDBM43837((4S,5R,6R)-1-(2-ethoxy-2-keto-ethyl)-2-keto-6-meth...)
Affinity DataKi:  7.00E+4nM ΔG°:  -23.7kJ/mole IC50:  3.00E+6nMT: 2°CAssay Description:Competitive inhibition assay for glucosamine derivatives on hexokinase from trypanosoma brucei. The inhibition of hexokinase by compounds was measur...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphotransferase(Trypanosoma brucei)
Universite Paul Sabatier

LigandPNGBDBM43836(Glucosamine derivative, 9 | MLS000580208 | N-(2,5-...)
Affinity DataKi:  1.00E+5nM ΔG°:  -22.8kJ/mole IC50:  4.00E+6nMT: 2°CAssay Description:Competitive inhibition assay for glucosamine derivatives on hexokinase from trypanosoma brucei. The inhibition of hexokinase by compounds was measur...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphotransferase(Trypanosoma brucei)
Universite Paul Sabatier

LigandPNGBDBM43829(Glucosamine derivative, 2 | MLS000568543 | SMR0001...)
Affinity DataKi:  1.00E+5nM ΔG°:  -22.8kJ/mole IC50:  6.00E+6nMT: 2°CAssay Description:Competitive inhibition assay for glucosamine derivatives on hexokinase from trypanosoma brucei. The inhibition of hexokinase by compounds was measur...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphotransferase(Trypanosoma brucei)
Universite Paul Sabatier

LigandPNGBDBM43830(5-(amoxymethyl)-3-[2-[(4-phenylthiazol-2-yl)hydraz...)
Affinity DataKi:  1.05E+5nM ΔG°:  -22.7kJ/mole IC50:  4.50E+6nMT: 2°CAssay Description:Competitive inhibition assay for glucosamine derivatives on hexokinase from trypanosoma brucei. The inhibition of hexokinase by compounds was measur...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphotransferase(Trypanosoma brucei)
Universite Paul Sabatier

LigandPNGBDBM43831(5-(4-fluorobenzyl)-4-keto-6,7-dihydropyrazolo[1,5-...)
Affinity DataKi:  1.14E+5nM ΔG°:  -22.5kJ/mole IC50:  1.80E+6nMT: 2°CAssay Description:Competitive inhibition assay for glucosamine derivatives on hexokinase from trypanosoma brucei. The inhibition of hexokinase by compounds was measur...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHexokinase-1(Saccharomyces cerevisiae)
Universite Paul Sabatier

LigandPNGBDBM85425(Glucosamine analog, 9)
Affinity DataIC50:  1.00E+6nMpH: 7.6 T: 2°CAssay Description:The assay phosphotransferase activity was followed spectrophotometrically b reduction of NADP in the presence of an excess of glucose-6-phosphate-deh...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHexokinase-1(Saccharomyces cerevisiae)
Universite Paul Sabatier

LigandPNGBDBM85423(Glucosamine analog, 7)
Affinity DataIC50:  3.00E+6nMpH: 7.6 T: 2°CAssay Description:The assay phosphotransferase activity was followed spectrophotometrically b reduction of NADP in the presence of an excess of glucose-6-phosphate-deh...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHexokinase-1(Saccharomyces cerevisiae)
Universite Paul Sabatier

LigandPNGBDBM85424(Glucosamine analog, 8)
Affinity DataIC50:  6.00E+6nMpH: 7.6 T: 2°CAssay Description:The assay phosphotransferase activity was followed spectrophotometrically b reduction of NADP in the presence of an excess of glucose-6-phosphate-deh...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHexokinase-1(Saccharomyces cerevisiae)
Universite Paul Sabatier

LigandPNGBDBM85426(Glucosamine analog, 10)
Affinity DataIC50:  6.00E+6nMpH: 7.6 T: 2°CAssay Description:The assay phosphotransferase activity was followed spectrophotometrically b reduction of NADP in the presence of an excess of glucose-6-phosphate-deh...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHexokinase-1(Saccharomyces cerevisiae)
Universite Paul Sabatier

LigandPNGBDBM85420(Glucosamine analog, 1)
Affinity DataIC50:  7.00E+6nMpH: 7.6 T: 2°CAssay Description:The assay phosphotransferase activity was followed spectrophotometrically b reduction of NADP in the presence of an excess of glucose-6-phosphate-deh...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphotransferase(Trypanosoma brucei)
Universite Paul Sabatier

LigandPNGBDBM43828(2-[(4-fluorobenzyl)thio]-N-(4,5,6,7-tetrahydro-1,3...)
Affinity DataIC50:  8.00E+6nMT: 2°CAssay Description:Competitive inhibition assay for glucosamine derivatives on hexokinase from trypanosoma brucei. The inhibition of hexokinase by compounds was measur...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHexokinase-1(Saccharomyces cerevisiae)
Universite Paul Sabatier

LigandPNGBDBM85421(Glucosamine analog, 2)
Affinity DataIC50:  8.00E+6nMpH: 7.6 T: 2°CAssay Description:The assay phosphotransferase activity was followed spectrophotometrically b reduction of NADP in the presence of an excess of glucose-6-phosphate-deh...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHexokinase-1(Saccharomyces cerevisiae)
Universite Paul Sabatier

LigandPNGBDBM85422(Glucosamine analog, 4)
Affinity DataIC50:  1.80E+7nMpH: 7.6 T: 2°CAssay Description:The assay phosphotransferase activity was followed spectrophotometrically b reduction of NADP in the presence of an excess of glucose-6-phosphate-deh...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed