TargetLow molecular weight phosphotyrosine protein phosphatase(Mus musculus)
University Of Campinas
Curated by ChEMBL
University Of Campinas
Curated by ChEMBL
Affinity DataKi: 4.70E+4nMAssay Description:Competitive inhibition of mouse LMW-PTP expressed in Escherichia coli using pNPP substrate by Dixon plotMore data for this Ligand-Target Pair
TargetLow molecular weight phosphotyrosine protein phosphatase(Mus musculus)
University Of Campinas
Curated by ChEMBL
University Of Campinas
Curated by ChEMBL
Affinity DataKi: 1.24E+5nMAssay Description:Competitive inhibition of mouse LMW-PTP expressed in Escherichia coli using pNPP substrate by Dixon plotMore data for this Ligand-Target Pair
TargetAlkaline phosphatase, placental type(Homo sapiens (Human))
University Of Campinas
Curated by ChEMBL
University Of Campinas
Curated by ChEMBL
Affinity DataKi: 5.80E+5nMAssay Description:Inhibition of human placental alkaline phosphatase using p-nitrophenyl phosphate substrateMore data for this Ligand-Target Pair
TargetEctonucleotide pyrophosphatase/phosphodiesterase family member 3(Bos taurus)
University Of Campinas
Curated by ChEMBL
University Of Campinas
Curated by ChEMBL
Affinity DataKi: 1.40E+6nMAssay Description:Inhibition of bovine intestinal 5'-nucleotide phosphodiesterase using 4-nitrophenyl phenylphosphonate substrate by spectrophotometryMore data for this Ligand-Target Pair
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
University Of Campinas
Curated by ChEMBL
University Of Campinas
Curated by ChEMBL
Affinity DataKi: 3.00E+6nMAssay Description:Inhibition of PTP1B (unknown origin) using nPP substrateMore data for this Ligand-Target Pair
Affinity DataIC50: 42nMAssay Description:Inhibition of human recombinant HDAC6 using ZMAL (Z-(Ac)Lys-AMC fluorogenic substrate incubated for 90 mins by fluorescence methodMore data for this Ligand-Target Pair
Affinity DataIC50: 120nMAssay Description:Inhibition of human recombinant HDAC1 using ZMAL (Z-(Ac)Lys-AMC fluorogenic substrate incubated for 90 mins by fluorescence methodMore data for this Ligand-Target Pair
Affinity DataIC50: 190nMAssay Description:Inhibition of human recombinant HDAC6 using ZMAL (Z-(Ac)Lys-AMC fluorogenic substrate incubated for 90 mins by fluorescence methodMore data for this Ligand-Target Pair
Affinity DataIC50: 215nMAssay Description:Inhibition of human recombinant HDAC6 using ZMAL (Z-(Ac)Lys-AMC fluorogenic substrate incubated for 90 mins by fluorescence methodMore data for this Ligand-Target Pair
Affinity DataIC50: 316nMAssay Description:Inhibition of human recombinant HDAC1 using ZMAL (Z-(Ac)Lys-AMC fluorogenic substrate incubated for 90 mins by fluorescence methodMore data for this Ligand-Target Pair
Affinity DataIC50: 775nMAssay Description:Inhibition of human recombinant HDAC1 using ZMAL (Z-(Ac)Lys-AMC fluorogenic substrate incubated for 90 mins by fluorescence methodMore data for this Ligand-Target Pair
TargetExtracellular superoxide dismutase [Cu-Zn](Homo sapiens (Human))
Universidad De Granada
Curated by ChEMBL
Universidad De Granada
Curated by ChEMBL
Affinity DataIC50: 8.92E+4nMAssay Description:Inhibition of human erythrocyte Cu-Zn SOD by NBT reduction assayMore data for this Ligand-Target Pair
TargetExtracellular superoxide dismutase [Cu-Zn](Homo sapiens (Human))
Universidad De Granada
Curated by ChEMBL
Universidad De Granada
Curated by ChEMBL
Affinity DataIC50: 9.66E+4nMAssay Description:Inhibition of human erythrocyte Cu-Zn SOD by NBT reduction assayMore data for this Ligand-Target Pair
TargetExtracellular superoxide dismutase [Cu-Zn](Homo sapiens (Human))
Universidad De Granada
Curated by ChEMBL
Universidad De Granada
Curated by ChEMBL
Affinity DataIC50: 1.55E+5nMAssay Description:Inhibition of human erythrocyte Cu-Zn SOD by NBT reduction assayMore data for this Ligand-Target Pair
TargetExtracellular superoxide dismutase [Cu-Zn](Homo sapiens (Human))
Universidad De Granada
Curated by ChEMBL
Universidad De Granada
Curated by ChEMBL
Affinity DataIC50: 2.74E+5nMAssay Description:Inhibition of human erythrocyte Cu-Zn SOD by NBT reduction assayMore data for this Ligand-Target Pair