Affinity DataKi: 20nMAssay Description:Competitive inhibition of thymidine phosphorylase (unknown origin)More data for this Ligand-Target Pair
Affinity DataKi: 40nMAssay Description:Inhibition of recombinant human liver CatL using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Universidade Estadual De Campinas
Curated by ChEMBL
Universidade Estadual De Campinas
Curated by ChEMBL
Affinity DataKi: 55nMAssay Description:Non-competitive inhibition of xanthine oxidase (unknown origin) by Lineweaver-Burk plot analysisMore data for this Ligand-Target Pair
Affinity DataKi: 79nMAssay Description:Inhibition of recombinant human liver CatS using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataKi: 158nMAssay Description:Inhibition of Trypanosoma cruzi cruzain using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataKi: 200nMAssay Description:Inhibition of Trypanosoma cruzi cruzain using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataKi: 251nMAssay Description:Inhibition of recombinant human liver CatK using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataKi: 251nMAssay Description:Inhibition of Trypanosoma cruzi cruzain using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataKi: 316nMAssay Description:Inhibition of recombinant human liver CatK using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataKi: 398nMAssay Description:Inhibition of recombinant human liver CatK using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataKi: 398nMAssay Description:Inhibition of recombinant human liver CatK using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck
Curated by ChEMBL
Merck
Curated by ChEMBL
Affinity DataKi: 530nMAssay Description:Inhibition of human ERG expressed in HEK293 cells at -80 mV holding potential by HPLC analysisMore data for this Ligand-Target Pair
Affinity DataKi: 631nMAssay Description:Inhibition of recombinant human liver CatL using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck
Curated by ChEMBL
Merck
Curated by ChEMBL
Affinity DataKi: 780nMAssay Description:Inhibition of human ERG expressed in HEK293 cells at -80 mV holding potential by HPLC analysisMore data for this Ligand-Target Pair
Affinity DataKi: 794nMAssay Description:Inhibition of recombinant human liver CatS using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck
Curated by ChEMBL
Merck
Curated by ChEMBL
Affinity DataKi: 1.30E+3nMAssay Description:Inhibition of human ERG expressed in HEK293 cells at -80 mV holding potential by HPLC analysisMore data for this Ligand-Target Pair
Affinity DataKi: 1.33E+3nMAssay Description:Inhibition of Varicella-Zoster virus DNA polymerase (95 uL) activity in a solution containing 6.4 mM HEPES (pH 7.5), incubation for 12 minutes at 26 ...More data for this Ligand-Target Pair
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Universidade Estadual De Campinas
Curated by ChEMBL
Universidade Estadual De Campinas
Curated by ChEMBL
Affinity DataKi: 1.55E+3nMAssay Description:Non-competitive inhibition of xanthine oxidase (unknown origin) by Lineweaver-Burk plot analysisMore data for this Ligand-Target Pair
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck
Curated by ChEMBL
Merck
Curated by ChEMBL
Affinity DataKi: 1.80E+3nMAssay Description:Inhibition of human ERG expressed in HEK293 cells at -80 mV holding potential by HPLC analysisMore data for this Ligand-Target Pair
Affinity DataKi: 2.00E+3nMAssay Description:Inhibition of recombinant human liver CatS using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataKi: 2.51E+3nMAssay Description:Inhibition of Trypanosoma cruzi cruzain using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataKi: 2.51E+3nMAssay Description:Inhibition of recombinant human liver CatL using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataKi: 2.51E+3nMAssay Description:Inhibition of recombinant human liver CatK using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck
Curated by ChEMBL
Merck
Curated by ChEMBL
Affinity DataKi: 3.10E+3nMAssay Description:Inhibition of human ERG expressed in HEK293 cells at -80 mV holding potential by HPLC analysisMore data for this Ligand-Target Pair
Affinity DataKi: 3.16E+3nMAssay Description:Inhibition of recombinant human liver CatL using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataKi: 3.16E+3nMAssay Description:Inhibition of Trypanosoma cruzi cruzain using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataKi: 3.16E+3nMAssay Description:Inhibition of recombinant human liver CatB using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataKi: 3.98E+3nMAssay Description:Inhibition of recombinant human liver CatB using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataKi: 3.98E+3nMAssay Description:Inhibition of recombinant human liver CatS using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataKi: 5.01E+3nMAssay Description:Inhibition of recombinant human liver CatS using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataKi: 5.01E+3nMAssay Description:Inhibition of Trypanosoma cruzi cruzain using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataKi: 5.01E+3nMAssay Description:Inhibition of recombinant human liver CatS using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataKi: 5.45E+3nMAssay Description:Binding affinity to recombinant human cathepsin KMore data for this Ligand-Target Pair
Affinity DataKi: 6.31E+3nMAssay Description:Inhibition of Trypanosoma cruzi cruzain using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataKi: 6.31E+3nMAssay Description:Inhibition of recombinant human liver CatS using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataKi: 6.31E+3nMAssay Description:Inhibition of recombinant human liver CatL using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataKi: 6.31E+3nMAssay Description:Inhibition of Trypanosoma cruzi cruzain using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataKi: 6.31E+3nMAssay Description:Inhibition of Trypanosoma cruzi cruzain using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataKi: 7.94E+3nMAssay Description:Inhibition of recombinant human liver CatB using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataKi: 7.94E+3nMAssay Description:Inhibition of recombinant human liver CatS using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataKi: 7.94E+3nMAssay Description:Inhibition of recombinant human liver CatB using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataKi: 7.94E+3nMAssay Description:Inhibition of Trypanosoma cruzi cruzain using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataKi: 9.57E+3nMAssay Description:Binding affinity to recombinant human cathepsin KMore data for this Ligand-Target Pair
Affinity DataKi: 1.00E+4nMAssay Description:Inhibition of recombinant human liver CatK using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataKi: 1.00E+4nMAssay Description:Inhibition of Trypanosoma cruzi cruzain using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataKi: 1.00E+4nMAssay Description:Inhibition of recombinant human liver CatL using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataKi: 1.00E+4nMAssay Description:Inhibition of recombinant human liver CatS using Z-FR-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
TargetGlyceraldehyde-3-phosphate dehydrogenase, glycosomal(Trypanosoma cruzi)
Da Universidade De S£O Paulo
Curated by ChEMBL
Da Universidade De S£O Paulo
Curated by ChEMBL
Affinity DataKi: 1.60E+4nMAssay Description:Competitive inhibition of Trypanosoma cruzi glycosomal GAPDH NAD+ binding site by ITC methodMore data for this Ligand-Target Pair
TargetGlyceraldehyde-3-phosphate dehydrogenase, glycosomal(Trypanosoma cruzi)
Da Universidade De S£O Paulo
Curated by ChEMBL
Da Universidade De S£O Paulo
Curated by ChEMBL
Affinity DataKi: 1.71E+4nMAssay Description:Competitive inhibition of Trypanosoma cruzi glycosomal GAPDH NAD+ binding site by ITC methodMore data for this Ligand-Target Pair
TargetGlyceraldehyde-3-phosphate dehydrogenase, glycosomal(Trypanosoma cruzi)
Da Universidade De S£O Paulo
Curated by ChEMBL
Da Universidade De S£O Paulo
Curated by ChEMBL
Affinity DataKi: 1.87E+4nMAssay Description:Competitive inhibition of Trypanosoma cruzi glycosomal GAPDH NAD+ binding site by ITC methodMore data for this Ligand-Target Pair