Affinity DataKi: 6.80E+3nMAssay Description:The promising ligand from the results obtained from ESI-MS assay are subjected to PPIase in vitro assay. The PPIase assay assesses the abil9ity of l...More data for this Ligand-Target Pair
Affinity DataKi: >1.00E+5nMAssay Description:The promising ligand from the results obtained from ESI-MS assay are subjected to PPIase in vitro assay. The PPIase assay assesses the abil9ity of l...More data for this Ligand-Target Pair
Affinity DataKi: >1.00E+5nMAssay Description:The promising ligand from the results obtained from ESI-MS assay are subjected to PPIase in vitro assay. The PPIase assay assesses the abil9ity of l...More data for this Ligand-Target Pair
Affinity DataKi: >1.00E+5nMAssay Description:The promising ligand from the results obtained from ESI-MS assay are subjected to PPIase in vitro assay. The PPIase assay assesses the abil9ity of l...More data for this Ligand-Target Pair
Affinity DataKi: >1.00E+5nMAssay Description:The promising ligand from the results obtained from ESI-MS assay are subjected to PPIase in vitro assay. The PPIase assay assesses the abil9ity of l...More data for this Ligand-Target Pair
Affinity DataKi: 2.07E+5nMAssay Description:The promising ligand from the results obtained from ESI-MS assay are subjected to PPIase in vitro assay. The PPIase assay assesses the abil9ity of l...More data for this Ligand-Target Pair
TargetATP-dependent 6-phosphofructokinase(Trypanosoma brucei)
University of Edinburgh
Curated by ChEMBL
University of Edinburgh
Curated by ChEMBL
Affinity DataIC50: 2.30E+4nMAssay Description:Inhibition of Trypanosoma brucei phosphofructokinaseMore data for this Ligand-Target Pair
Affinity DataIC50: 2.60E+4nMAssay Description:Inhibition of Leishmania mexicana pyruvate kinaseMore data for this Ligand-Target Pair
TargetATP-dependent 6-phosphofructokinase(Trypanosoma brucei)
University of Edinburgh
Curated by ChEMBL
University of Edinburgh
Curated by ChEMBL
Affinity DataIC50: 4.90E+4nMAssay Description:Inhibition of Trypanosoma brucei phosphofructokinaseMore data for this Ligand-Target Pair
TargetATP-dependent 6-phosphofructokinase(Trypanosoma brucei)
University of Edinburgh
Curated by ChEMBL
University of Edinburgh
Curated by ChEMBL
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of Trypanosoma brucei phosphofructokinaseMore data for this Ligand-Target Pair
Affinity DataIC50: 5.30E+4nMAssay Description:Inhibition of Leishmania mexicana pyruvate kinaseMore data for this Ligand-Target Pair
Affinity DataIC50: 7.10E+4nMAssay Description:Inhibition of Leishmania mexicana pyruvate kinaseMore data for this Ligand-Target Pair
TargetATP-dependent 6-phosphofructokinase(Trypanosoma brucei)
University of Edinburgh
Curated by ChEMBL
University of Edinburgh
Curated by ChEMBL
Affinity DataIC50: 8.00E+4nMAssay Description:Inhibition of Trypanosoma brucei phosphofructokinaseMore data for this Ligand-Target Pair
TargetGamma-aminobutyric acid receptor subunit alpha-2/beta-2/gamma-2(Homo sapiens (Human))
Novartis Institutes for BioMedical Research
Curated by ChEMBL
Novartis Institutes for BioMedical Research
Curated by ChEMBL
Affinity DataIC50: 1.90E+5nMAssay Description:Inhibition of recombinant human GABA A alpha2beta2gamma2 receptor expressed in CHO-K1 cells incubated at room temperature for 15 mins before the GABA...More data for this Ligand-Target Pair
TargetATP-dependent 6-phosphofructokinase(Trypanosoma brucei)
University of Edinburgh
Curated by ChEMBL
University of Edinburgh
Curated by ChEMBL
Affinity DataIC50: 4.10E+5nMAssay Description:Inhibition of Trypanosoma brucei phosphofructokinaseMore data for this Ligand-Target Pair
TargetGamma-aminobutyric acid receptor subunit alpha-2/beta-2/gamma-2(Homo sapiens (Human))
Novartis Institutes for BioMedical Research
Curated by ChEMBL
Novartis Institutes for BioMedical Research
Curated by ChEMBL
Affinity DataIC50: 8.90E+5nMAssay Description:Inhibition of recombinant human GABA A alpha2beta2gamma2 receptor expressed in CHO-K1 cells incubated at room temperature for 15 mins before the GABA...More data for this Ligand-Target Pair
Affinity DataIC50: 9.00E+5nMAssay Description:Inhibition of Leishmania mexicana pyruvate kinaseMore data for this Ligand-Target Pair
Affinity DataIC50: 1.20E+6nMAssay Description:Inhibition of Leishmania mexicana pyruvate kinaseMore data for this Ligand-Target Pair
TargetGamma-aminobutyric acid receptor subunit alpha-2/beta-2/gamma-2(Homo sapiens (Human))
Novartis Institutes for BioMedical Research
Curated by ChEMBL
Novartis Institutes for BioMedical Research
Curated by ChEMBL
Affinity DataIC50: 1.34E+6nMAssay Description:Inhibition of recombinant human GABA A alpha2beta2gamma2 receptor expressed in CHO-K1 cells incubated at room temperature for 15 mins before the GABA...More data for this Ligand-Target Pair
Affinity DataIC50: 1.50E+6nMAssay Description:Inhibition of Leishmania mexicana pyruvate kinaseMore data for this Ligand-Target Pair
Affinity DataIC50: 1.50E+6nMAssay Description:Inhibition of Leishmania mexicana pyruvate kinaseMore data for this Ligand-Target Pair
Affinity DataIC50: 1.50E+6nMAssay Description:Inhibition of Leishmania mexicana pyruvate kinaseMore data for this Ligand-Target Pair
Affinity DataIC50: 2.30E+6nMAssay Description:Inhibition of Leishmania mexicana pyruvate kinaseMore data for this Ligand-Target Pair
TargetGamma-aminobutyric acid receptor subunit alpha-2/beta-2/gamma-2(Homo sapiens (Human))
Novartis Institutes for BioMedical Research
Curated by ChEMBL
Novartis Institutes for BioMedical Research
Curated by ChEMBL
Affinity DataIC50: 2.40E+6nMAssay Description:Inhibition of recombinant human GABA A alpha2beta2gamma2 receptor expressed in CHO-K1 cells incubated at room temperature for 15 mins before the GABA...More data for this Ligand-Target Pair
Affinity DataIC50: 2.50E+6nMAssay Description:Inhibition of Leishmania mexicana pyruvate kinaseMore data for this Ligand-Target Pair
Affinity DataIC50: 3.50E+6nMAssay Description:Inhibition of Leishmania mexicana pyruvate kinaseMore data for this Ligand-Target Pair
Affinity DataIC50: 4.10E+6nMAssay Description:Inhibition of Leishmania mexicana pyruvate kinaseMore data for this Ligand-Target Pair
Affinity DataIC50: 4.30E+6nMAssay Description:Inhibition of Leishmania mexicana pyruvate kinaseMore data for this Ligand-Target Pair
Affinity DataKd: 1.33E+5nMAssay Description:Electrospray mass spectrometry assay is a immunophilin-ligand binding assay which allows us to rapidly probe the affinity of potential inhibitors for...More data for this Ligand-Target Pair
Affinity DataKd: 1.13E+5nMAssay Description:Electrospray mass spectrometry assay is a immunophilin-ligand binding assay which allows us to rapidly probe the affinity of potential inhibitors for...More data for this Ligand-Target Pair
Affinity DataKd: 8.51E+4nMAssay Description:Electrospray mass spectrometry assay is a immunophilin-ligand binding assay which allows us to rapidly probe the affinity of potential inhibitors for...More data for this Ligand-Target Pair
Affinity DataKd: 3.19E+4nMAssay Description:Electrospray mass spectrometry assay is a immunophilin-ligand binding assay which allows us to rapidly probe the affinity of potential inhibitors for...More data for this Ligand-Target Pair
Affinity DataKd: 7.26E+4nMAssay Description:Electrospray mass spectrometry assay is a immunophilin-ligand binding assay which allows us to rapidly probe the affinity of potential inhibitors for...More data for this Ligand-Target Pair
Affinity DataKd: 1.28E+5nMAssay Description:Electrospray mass spectrometry assay is a immunophilin-ligand binding assay which allows us to rapidly probe the affinity of potential inhibitors for...More data for this Ligand-Target Pair
Affinity DataKd: 2.28E+4nMAssay Description:The promising ligand from the results obtained from ESI-MS assay are subjected to fluorescence in vitro assay. The fluorescence assay takes advantag...More data for this Ligand-Target Pair
Affinity DataKd: 1.59E+4nMAssay Description:The promising ligand from the results obtained from ESI-MS assay are subjected to fluorescence in vitro assay. The fluorescence assay takes advantag...More data for this Ligand-Target Pair
Affinity DataKd: 2.96E+4nMAssay Description:The promising ligand from the results obtained from ESI-MS assay are subjected to fluorescence in vitro assay. The fluorescence assay takes advantag...More data for this Ligand-Target Pair
Affinity DataKd: >5.00E+4nMAssay Description:The promising ligand from the results obtained from ESI-MS assay are subjected to fluorescence in vitro assay. The fluorescence assay takes advantag...More data for this Ligand-Target Pair
Affinity DataKd: 2.19E+4nMAssay Description:The promising ligand from the results obtained from ESI-MS assay are subjected to fluorescence in vitro assay. The fluorescence assay takes advantag...More data for this Ligand-Target Pair
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