TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: 30nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: 360nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: 480nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: 900nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: 1.60E+3nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: 1.70E+3nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: 1.80E+3nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: 2.60E+3nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: 2.90E+3nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: 3.00E+3nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: 3.20E+3nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: 3.70E+3nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: 4.00E+3nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: 4.90E+3nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: 5.00E+3nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: 5.30E+3nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: 5.60E+3nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: 6.20E+3nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: 7.70E+3nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: 9.80E+3nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: 1.10E+4nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: 1.19E+4nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: 1.40E+4nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: 3.50E+4nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: 4.20E+4nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: 5.00E+4nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of IRAP in HEKT cells assessed as hydrolysis of L-leucine-4-methyl-7-coumarinylamide after 30 minsMore data for this Ligand-Target Pair
TargetGlucocorticoid receptor(Homo sapiens (Human))
Monash University (Parkville Campus)
Curated by ChEMBL
Monash University (Parkville Campus)
Curated by ChEMBL
Affinity DataIC50: 14nMAssay Description:Inhibition of human glucocorticoid receptorMore data for this Ligand-Target Pair
TargetDihydroorotate dehydrogenase (quinone), mitochondrial(Plasmodium falciparum)
University Of Washington
Curated by ChEMBL
University Of Washington
Curated by ChEMBL
Affinity DataIC50: 35nMAssay Description:Inhibition of His6-tagged recombinant Plasmodium falciparum dihydroorotate dehydrogenase expressed in Escherichia coli using L-dihydroorotate as subs...More data for this Ligand-Target Pair
TargetDihydroorotate dehydrogenase (quinone), mitochondrial(Plasmodium falciparum (isolate 3D7))
University Of Washington At Seattle
University Of Washington At Seattle
Affinity DataIC50: 47nMpH: 8.0 T: 2°CAssay Description:The assays were carried out by using a colorimetric DCIP method, which uses the colorimetric reagent 2, 6-dichlorophenolindophenol as the final elect...More data for this Ligand-Target Pair
TargetDihydroorotate dehydrogenase (quinone), mitochondrial(Plasmodium falciparum (isolate 3D7))
University Of Washington At Seattle
University Of Washington At Seattle
Affinity DataIC50: 56nMpH: 8.0 T: 2°CAssay Description:The assays were carried out by using a colorimetric DCIP method, which uses the colorimetric reagent 2, 6-dichlorophenolindophenol as the final elect...More data for this Ligand-Target Pair
TargetDihydroorotate dehydrogenase (quinone), mitochondrial(Plasmodium falciparum)
University Of Washington
Curated by ChEMBL
University Of Washington
Curated by ChEMBL
Affinity DataIC50: 64nMAssay Description:Inhibition of His6-tagged recombinant Plasmodium falciparum dihydroorotate dehydrogenase expressed in Escherichia coli using L-dihydroorotate as subs...More data for this Ligand-Target Pair
TargetDihydroorotate dehydrogenase (quinone), mitochondrial(Plasmodium falciparum (isolate 3D7))
University Of Washington At Seattle
University Of Washington At Seattle
Affinity DataIC50: 77nMAssay Description:The assays were carried out by using a colorimetric DCIP method, which uses the colorimetric reagent 2, 6-dichlorophenolindophenol as the final elect...More data for this Ligand-Target Pair
TargetDihydroorotate dehydrogenase (quinone), mitochondrial(Plasmodium falciparum)
University Of Washington
Curated by ChEMBL
University Of Washington
Curated by ChEMBL
Affinity DataIC50: 78nMAssay Description:Inhibition of His6-tagged recombinant Plasmodium falciparum dihydroorotate dehydrogenase expressed in Escherichia coli using L-dihydroorotate as subs...More data for this Ligand-Target Pair
TargetDihydroorotate dehydrogenase (quinone), mitochondrial(Plasmodium falciparum)
University Of Washington
Curated by ChEMBL
University Of Washington
Curated by ChEMBL
Affinity DataIC50: 90nMAssay Description:Inhibition of His6-tagged recombinant Plasmodium falciparum dihydroorotate dehydrogenase expressed in Escherichia coli using L-dihydroorotate as subs...More data for this Ligand-Target Pair
TargetCytochrome P450 2C19(Homo sapiens (Human))
University of Nebraska Medical Center
Curated by ChEMBL
University of Nebraska Medical Center
Curated by ChEMBL
Affinity DataIC50: 110nMAssay Description:Inhibition of CYP2C19More data for this Ligand-Target Pair
TargetDihydroorotate dehydrogenase (quinone), mitochondrial(Plasmodium falciparum)
University Of Washington
Curated by ChEMBL
University Of Washington
Curated by ChEMBL
Affinity DataIC50: 130nMAssay Description:Inhibition of His6-tagged recombinant Plasmodium falciparum dihydroorotate dehydrogenase expressed in Escherichia coli using L-dihydroorotate as subs...More data for this Ligand-Target Pair