Compile Data Set for Download or QSAR
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Found 10 of ki for UniProtKB: Q38C42
TargetPhosphotransferase(Trypanosoma brucei)
Universite Paul Sabatier

LigandPNGBDBM43835(Glucosamine derivative, 8 | MLS000582359 | N-cyclo...)
Affinity DataKi:  2.80E+3nM ΔG°:  -7.57kcal/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°:  -6.95kcal/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°:  -6.44kcal/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°:  -6.27kcal/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°:  -6.17kcal/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°:  -5.66kcal/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°:  -5.45kcal/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°:  -5.45kcal/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°:  -5.42kcal/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°:  -5.38kcal/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