TargetCruzipain(Trypanosoma cruzi)
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
Affinity DataKi: 1.60nMAssay Description:Covalent inhibition of Trypanosoma cruzi cruzipain using Z-Phe-Arg-7-amidomethylcoumarin as substrate measured after 30 mins by fluorometric analysisMore data for this Ligand-Target Pair
TargetCruzipain(Trypanosoma cruzi)
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
Affinity DataKi: 2nMAssay Description:Covalent inhibition of Trypanosoma cruzi cruzipain using Z-Phe-Arg-7-amidomethylcoumarin as substrate measured after 30 mins by fluorometric analysisMore data for this Ligand-Target Pair
TargetCruzipain(Trypanosoma cruzi)
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
Affinity DataKi: 251nMAssay Description:Covalent inhibition of Trypanosoma cruzi cruzipain using Z-Phe-Arg-7-amidomethylcoumarin as substrate measured after 5 mins by fluorometric analysisMore data for this Ligand-Target Pair
TargetCruzipain(Trypanosoma cruzi)
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
Affinity DataKi: 501nMAssay Description:Covalent inhibition of Trypanosoma cruzi cruzipain using Z-Phe-Arg-7-amidomethylcoumarin as substrate measured after 5 mins by fluorometric analysisMore data for this Ligand-Target Pair
TargetCruzipain(Trypanosoma cruzi)
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
Affinity DataKi: 501nMAssay Description:Covalent inhibition of Trypanosoma cruzi cruzipain using Z-Phe-Arg-7-amidomethylcoumarin as substrate measured after 5 mins by fluorometric analysisMore data for this Ligand-Target Pair
TargetCruzipain(Trypanosoma cruzi)
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
Affinity DataKi: 3.98E+3nMAssay Description:Covalent inhibition of Trypanosoma cruzi cruzipain using Z-Phe-Arg-7-amidomethylcoumarin as substrate measured after 5 mins by fluorometric analysisMore data for this Ligand-Target Pair
TargetCruzipain(Trypanosoma cruzi)
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
Affinity DataKi: 6.31E+3nMAssay Description:Covalent inhibition of Trypanosoma cruzi cruzipain using Z-Phe-Arg-7-amidomethylcoumarin as substrate measured after 5 mins by fluorometric analysisMore data for this Ligand-Target Pair
TargetCruzipain(Trypanosoma cruzi)
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
Affinity DataKi: 1.00E+4nMAssay Description:Covalent inhibition of Trypanosoma cruzi cruzipain using Z-Phe-Arg-7-amidomethylcoumarin as substrate measured after 5 mins by fluorometric analysisMore data for this Ligand-Target Pair
TargetCruzipain(Trypanosoma cruzi)
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
Affinity DataKi: 1.00E+4nMAssay Description:Covalent inhibition of Trypanosoma cruzi cruzipain using Z-Phe-Arg-7-amidomethylcoumarin as substrate measured after 5 mins by fluorometric analysisMore data for this Ligand-Target Pair
TargetCruzipain(Trypanosoma cruzi)
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
Affinity DataKi: 1.00E+4nMAssay Description:Covalent inhibition of Trypanosoma cruzi cruzipain using Z-Phe-Arg-7-amidomethylcoumarin as substrate measured after 5 mins by fluorometric analysisMore data for this Ligand-Target Pair
TargetCruzipain(Trypanosoma cruzi)
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
Affinity DataKi: 2.00E+4nMAssay Description:Covalent inhibition of Trypanosoma cruzi cruzipain using Z-Phe-Arg-7-amidomethylcoumarin as substrate measured after 5 mins by fluorometric analysisMore data for this Ligand-Target Pair
TargetCruzipain(Trypanosoma cruzi)
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
Affinity DataKi: 2.51E+4nMAssay Description:Covalent inhibition of Trypanosoma cruzi cruzipain using Z-Phe-Arg-7-amidomethylcoumarin as substrate measured after 5 mins by fluorometric analysisMore data for this Ligand-Target Pair
TargetCruzipain(Trypanosoma cruzi)
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
Affinity DataKi: 1.00E+5nMAssay Description:Covalent inhibition of Trypanosoma cruzi cruzipain using Z-Phe-Arg-7-amidomethylcoumarin as substrate measured after 5 mins by fluorometric analysisMore data for this Ligand-Target Pair
TargetCruzipain(Trypanosoma cruzi)
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
Affinity DataKi: 1.26E+5nMAssay Description:Covalent inhibition of Trypanosoma cruzi cruzipain using Z-Phe-Arg-7-amidomethylcoumarin as substrate measured after 5 mins by fluorometric analysisMore data for this Ligand-Target Pair
TargetCruzipain(Trypanosoma cruzi)
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
Affinity DataKi: 2.00E+5nMAssay Description:Covalent inhibition of Trypanosoma cruzi cruzipain using Z-Phe-Arg-7-amidomethylcoumarin as substrate measured after 5 mins by fluorometric analysisMore data for this Ligand-Target Pair
TargetCruzipain(Trypanosoma cruzi)
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
University Of S£O Paulo Avenue Trabalhador Sancarlense
Curated by ChEMBL
Affinity DataKi: 3.98E+5nMAssay Description:Covalent inhibition of Trypanosoma cruzi cruzipain using Z-Phe-Arg-7-amidomethylcoumarin as substrate measured after 5 mins by fluorometric analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 10nMAssay Description:Inhibition of CYP2D6 after 30 mins by fluorometric assayMore data for this Ligand-Target Pair
Affinity DataIC50: 78nMAssay Description:Inhibition of human CYP2D6 by radiometric assayMore data for this Ligand-Target Pair
Affinity DataIC50: 82nMAssay Description:Inhibition of human liver microsome CYP2D6 in assessed as [14C]formaldehyde formationMore data for this Ligand-Target Pair
Affinity DataIC50: 200nMAssay Description:Inhibition of CYP3A4 after 30 mins by fluorometric assayMore data for this Ligand-Target Pair
Affinity DataIC50: 440nMAssay Description:Inhibition of human liver microsome CYP3A4 in assessed as [14C]formaldehyde formationMore data for this Ligand-Target Pair
Affinity DataIC50: 800nMAssay Description:Inhibition of human liver microsome CYP3A4 in assessed as [14C]formaldehyde formationMore data for this Ligand-Target Pair
Affinity DataIC50: 830nMAssay Description:Inhibition of human liver microsome CYP3A4 in assessed as [14C]formaldehyde formationMore data for this Ligand-Target Pair
Affinity DataIC50: 830nMAssay Description:Inhibition of human liver microsome CYP3A4 in assessed as [14C]formaldehyde formationMore data for this Ligand-Target Pair
Affinity DataIC50: 960nMAssay Description:Inhibitory activity against Glucosylceramidase in mouse liverMore data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of human liver microsome CYP3A4 in assessed as [14C]formaldehyde formationMore data for this Ligand-Target Pair
Affinity DataIC50: 1.10E+3nMAssay Description:Inhibition of human liver microsome CYP3A4 in assessed as [14C]formaldehyde formationMore data for this Ligand-Target Pair
TargetTyrosine-protein phosphatase non-receptor type 2(Homo sapiens (Human))
University Of Toyama
Curated by ChEMBL
University Of Toyama
Curated by ChEMBL
Affinity DataIC50: 2.40E+3nMAssay Description:Inhibition of TCPTP (unknown origin) assessed as decrease in p-nitrophenol production from pNPP substrate after 30 mins by HTS7000 bioassay reader an...More data for this Ligand-Target Pair
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
University Of Toyama
Curated by ChEMBL
University Of Toyama
Curated by ChEMBL
Affinity DataIC50: 2.75E+3nMAssay Description:Inhibition of PTP1B (unknown origin) assessed as decrease in p-nitrophenol production from pNPP substrate after 30 mins by HTS7000 bioassay reader an...More data for this Ligand-Target Pair
Affinity DataIC50: 4.63E+3nMAssay Description:Inhibition of human CYP2D6 by radiometric assayMore data for this Ligand-Target Pair
TargetTyrosine-protein phosphatase non-receptor type 2(Homo sapiens (Human))
University Of Toyama
Curated by ChEMBL
University Of Toyama
Curated by ChEMBL
Affinity DataIC50: 5.10E+3nMAssay Description:Inhibition of TCPTP (unknown origin) assessed as decrease in p-nitrophenol production from pNPP substrate after 30 mins by HTS7000 bioassay reader an...More data for this Ligand-Target Pair
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
University Of Toyama
Curated by ChEMBL
University Of Toyama
Curated by ChEMBL
Affinity DataIC50: 5.62E+3nMAssay Description:Inhibition of PTP1B (unknown origin) assessed as decrease in p-nitrophenol production from pNPP substrate after 30 mins by HTS7000 bioassay reader an...More data for this Ligand-Target Pair
TargetBeta-glucuronidase(Bos taurus (Bovine))
Toyama Medical and Pharmaceutical University
Curated by ChEMBL
Toyama Medical and Pharmaceutical University
Curated by ChEMBL
Affinity DataIC50: 6.80E+3nMAssay Description:Inhibition of bovine beta-glucuronidaseMore data for this Ligand-Target Pair
Affinity DataIC50: 7.40E+3nMAssay Description:Inhibition of human liver microsome CYP3A4 in assessed as [14C]formaldehyde formationMore data for this Ligand-Target Pair
TargetTyrosine-protein phosphatase non-receptor type 2(Homo sapiens (Human))
University Of Toyama
Curated by ChEMBL
University Of Toyama
Curated by ChEMBL
Affinity DataIC50: 7.40E+3nMAssay Description:Inhibition of TCPTP (unknown origin) assessed as decrease in p-nitrophenol production from pNPP substrate after 30 mins by HTS7000 bioassay reader an...More data for this Ligand-Target Pair
Affinity DataIC50: 7.70E+3nMAssay Description:Inhibition of human liver microsome CYP3A4 in assessed as [14C]formaldehyde formationMore data for this Ligand-Target Pair
Affinity DataIC50: 8.00E+3nMAssay Description:Inhibition of human liver microsome CYP3A4 in assessed as [14C]formaldehyde formationMore data for this Ligand-Target Pair
Affinity DataIC50: 8.80E+3nMAssay Description:Inhibition of human liver microsome CYP3A4 in assessed as [14C]formaldehyde formationMore data for this Ligand-Target Pair
Affinity DataIC50: 8.90E+3nMAssay Description:Specific inhibitory activity against Glucosylceramidase in mouse liverMore data for this Ligand-Target Pair
Affinity DataIC50: 9.10E+3nMAssay Description:Inhibition of human liver microsome CYP3A4 in assessed as [14C]formaldehyde formationMore data for this Ligand-Target Pair
TargetTyrosine-protein phosphatase non-receptor type 2(Homo sapiens (Human))
University Of Toyama
Curated by ChEMBL
University Of Toyama
Curated by ChEMBL
Affinity DataIC50: 9.30E+3nMAssay Description:Inhibition of TCPTP (unknown origin) assessed as decrease in p-nitrophenol production from pNPP substrate after 30 mins by HTS7000 bioassay reader an...More data for this Ligand-Target Pair
Affinity DataIC50: 9.50E+3nMAssay Description:Inhibition of human liver microsome CYP3A4 in assessed as [14C]formaldehyde formationMore data for this Ligand-Target Pair
TargetBeta-glucuronidase(Bos taurus (Bovine))
Toyama Medical and Pharmaceutical University
Curated by ChEMBL
Toyama Medical and Pharmaceutical University
Curated by ChEMBL
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of bovine beta-glucuronidaseMore data for this Ligand-Target Pair
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
University Of Toyama
Curated by ChEMBL
University Of Toyama
Curated by ChEMBL
Affinity DataIC50: 1.04E+4nMAssay Description:Inhibition of PTP1B (unknown origin) assessed as decrease in p-nitrophenol production from pNPP substrate after 30 mins by HTS7000 bioassay reader an...More data for this Ligand-Target Pair
Affinity DataIC50: 1.37E+4nMAssay Description:Inhibition of human liver microsome CYP3A4 in assessed as [14C]formaldehyde formationMore data for this Ligand-Target Pair
Affinity DataIC50: 1.44E+4nMAssay Description:Inhibition of human CYP3A4 by radiometric assayMore data for this Ligand-Target Pair
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
University Of Toyama
Curated by ChEMBL
University Of Toyama
Curated by ChEMBL
Affinity DataIC50: 1.47E+4nMAssay Description:Inhibition of PTP1B (unknown origin) assessed as decrease in p-nitrophenol production from pNPP substrate after 30 mins by HTS7000 bioassay reader an...More data for this Ligand-Target Pair
Affinity DataIC50: 1.49E+4nMAssay Description:Inhibition of human liver microsome CYP3A4 in assessed as [14C]formaldehyde formationMore data for this Ligand-Target Pair
Affinity DataIC50: 1.50E+4nMAssay Description:Inhibition of human liver microsome CYP3A4 in assessed as [14C]formaldehyde formationMore data for this Ligand-Target Pair
TargetTyrosine-protein phosphatase non-receptor type 2(Homo sapiens (Human))
University Of Toyama
Curated by ChEMBL
University Of Toyama
Curated by ChEMBL
Affinity DataIC50: 1.57E+4nMAssay Description:Inhibition of TCPTP (unknown origin) assessed as decrease in p-nitrophenol production from pNPP substrate after 30 mins by HTS7000 bioassay reader an...More data for this Ligand-Target Pair