TargetProteasome subunit beta type-5(Homo sapiens (Human))
The University Of Melbourne
Curated by ChEMBL
The University Of Melbourne
Curated by ChEMBL
Affinity DataKi: 0.130nMAssay Description:Binding affinity to human 20S constitutive proteasome beta 5 subunit assessed as equilibrium constant using fluorogenic peptide Ac-WLA-AMC as substra...More data for this Ligand-Target Pair
Affinity DataKi: 0.158nMAssay Description:Displacement of [125I]-DOI from recombinant human 5HT2CR transfected in human HEK293 cells incubated for 45 mins by radioligand binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 0.251nMAssay Description:Displacement of [125I]-DOI from recombinant human 5HT2CR transfected in human HEK293 cells incubated for 45 mins by radioligand binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 0.316nMAssay Description:Displacement of [125I]-DOI from recombinant human 5HT2CR transfected in human HEK293 cells incubated for 45 mins by radioligand binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 0.501nMAssay Description:Displacement of [125I]-DOI from recombinant human 5HT2CR transfected in human HEK293 cells incubated for 45 mins by radioligand binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 0.501nMAssay Description:Displacement of [125I]-DOI from recombinant human 5HT2CR transfected in human HEK293 cells incubated for 45 mins by radioligand binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 0.631nMAssay Description:Displacement of [125I]-DOI from recombinant human 5HT2CR transfected in human HEK293 cells incubated for 45 mins by radioligand binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 1.30nMAssay Description:Displacement of [3H]-DOI from recombinant human 5HT2AR transfected in human HEK293 cells incubated for 45 mins by radioligand binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 1.60nMAssay Description:Displacement of [125I]-DOI from recombinant human 5HT2CR transfected in human HEK293 cells incubated for 45 mins by radioligand binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 2nMAssay Description:Displacement of [125I]-DOI from recombinant human 5HT2CR transfected in human HEK293 cells incubated for 45 mins by radioligand binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 2nMAssay Description:Displacement of [125I]-DOI from recombinant human 5HT2CR transfected in human HEK293 cells incubated for 45 mins by radioligand binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 2.5nMAssay Description:Displacement of [3H]-DOI from recombinant human 5HT2AR transfected in human HEK293 cells incubated for 45 mins by radioligand binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 5nMAssay Description:Displacement of [3H]-DOI from recombinant human 5HT2AR transfected in human HEK293 cells incubated for 45 mins by radioligand binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 6.30nMAssay Description:Displacement of [3H]-DOI from recombinant human 5HT2AR transfected in human HEK293 cells incubated for 45 mins by radioligand binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 10nMAssay Description:Displacement of [125I]-DOI from recombinant human 5HT2CR transfected in human HEK293 cells incubated for 45 mins by radioligand binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 10nMAssay Description:Displacement of [3H]-LSB from recombinant human 5HT2BR transfected in human HEK293 cells incubated for 45 mins by radioligand binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 13nMAssay Description:Displacement of [3H]-LSB from recombinant human 5HT2BR transfected in human HEK293 cells incubated for 45 mins by radioligand binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 13nMAssay Description:Displacement of [3H]-DOI from recombinant human 5HT2AR transfected in human HEK293 cells incubated for 45 mins by radioligand binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 20nMAssay Description:Displacement of [3H]-DOI from recombinant human 5HT2AR transfected in human HEK293 cells incubated for 45 mins by radioligand binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 25nMAssay Description:Displacement of [3H]-LSB from recombinant human 5HT2BR transfected in human HEK293 cells incubated for 45 mins by radioligand binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 25nMAssay Description:Displacement of [3H]-DOI from recombinant human 5HT2AR transfected in human HEK293 cells incubated for 45 mins by radioligand binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 32nMAssay Description:Displacement of [3H]-LSB from recombinant human 5HT2BR transfected in human HEK293 cells incubated for 45 mins by radioligand binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 40nMAssay Description:Displacement of [3H]-LSB from recombinant human 5HT2BR transfected in human HEK293 cells incubated for 45 mins by radioligand binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 40nMAssay Description:Displacement of [3H]-DOI from recombinant human 5HT2AR transfected in human HEK293 cells incubated for 45 mins by radioligand binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 50nMAssay Description:Displacement of [3H]-DOI from recombinant human 5HT2AR transfected in human HEK293 cells incubated for 45 mins by radioligand binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 100nMAssay Description:Displacement of [3H]-DOI from recombinant human 5HT2AR transfected in human HEK293 cells incubated for 45 mins by radioligand binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 100nMAssay Description:Displacement of [3H]-LSB from recombinant human 5HT2BR transfected in human HEK293 cells incubated for 45 mins by radioligand binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 126nMAssay Description:Displacement of [3H]-LSB from recombinant human 5HT2BR transfected in human HEK293 cells incubated for 45 mins by radioligand binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 126nMAssay Description:Displacement of [3H]-LSB from recombinant human 5HT2BR transfected in human HEK293 cells incubated for 45 mins by radioligand binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 200nMAssay Description:Displacement of [3H]-LSB from recombinant human 5HT2BR transfected in human HEK293 cells incubated for 45 mins by radioligand binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 251nMAssay Description:Displacement of [3H]-LSB from recombinant human 5HT2BR transfected in human HEK293 cells incubated for 45 mins by radioligand binding assayMore data for this Ligand-Target Pair
TargetProteasome subunit beta type-2(Homo sapiens (Human))
The University Of Melbourne
Curated by ChEMBL
The University Of Melbourne
Curated by ChEMBL
Affinity DataKi: 487nMAssay Description:Binding affinity to human 20S constitutive proteasome beta 2 subunit assessed as equilibrium constant using fluorogenic peptide Ac-WLR-AMC as substra...More data for this Ligand-Target Pair
Target4-hydroxy-tetrahydrodipicolinate synthase(Escherichia coli (strain K12))
University Of Melbourne
Curated by ChEMBL
University Of Melbourne
Curated by ChEMBL
Affinity DataKi: 1.60E+4nMAssay Description:Inhibition of Escherichia coli DHDPSMore data for this Ligand-Target Pair
Target4-hydroxy-tetrahydrodipicolinate synthase(Bacillus subtilis)
University Of Melbourne
Curated by ChEMBL
University Of Melbourne
Curated by ChEMBL
Affinity DataKi: 1.60E+5nMAssay Description:Inhibition of Bacillus subtilis DHDPSMore data for this Ligand-Target Pair
Target4-hydroxy-tetrahydrodipicolinate synthase(Escherichia coli (strain K12))
University Of Melbourne
Curated by ChEMBL
University Of Melbourne
Curated by ChEMBL
Affinity DataKi: 1.70E+5nMAssay Description:Inhibition of Escherichia coli DHDPSMore data for this Ligand-Target Pair
Target4-hydroxy-tetrahydrodipicolinate synthase(Escherichia coli (strain K12))
University Of Melbourne
Curated by ChEMBL
University Of Melbourne
Curated by ChEMBL
Affinity DataKi: 1.70E+5nMAssay Description:Binding affinity for Escherichia coli dihydrodipicolinate synthaseMore data for this Ligand-Target Pair
Target4-hydroxy-2-oxoglutarate aldolase, mitochondrial(Homo sapiens (Human))
University Of Melbourne
Curated by ChEMBL
University Of Melbourne
Curated by ChEMBL
Affinity DataKi: 1.70E+5nMAssay Description:Inhibition of dihydrodipicolinate synthaseMore data for this Ligand-Target Pair
Target4-hydroxy-2-oxoglutarate aldolase, mitochondrial(Homo sapiens (Human))
University Of Melbourne
Curated by ChEMBL
University Of Melbourne
Curated by ChEMBL
Affinity DataKi: 1.70E+5nMAssay Description:Inhibition of dihydrodipicolinate synthaseMore data for this Ligand-Target Pair
Target4-hydroxy-tetrahydrodipicolinate synthase(Escherichia coli (strain K12))
University Of Melbourne
Curated by ChEMBL
University Of Melbourne
Curated by ChEMBL
Affinity DataKi: 2.20E+5nMAssay Description:Inhibition of Escherichia coli DHDPSMore data for this Ligand-Target Pair
Target4-hydroxy-2-oxoglutarate aldolase, mitochondrial(Homo sapiens (Human))
University Of Melbourne
Curated by ChEMBL
University Of Melbourne
Curated by ChEMBL
Affinity DataKi: 3.30E+5nMAssay Description:Inhibition of dihydrodipicolinate synthaseMore data for this Ligand-Target Pair
Target4-hydroxy-tetrahydrodipicolinate synthase(Escherichia coli (strain K12))
University Of Melbourne
Curated by ChEMBL
University Of Melbourne
Curated by ChEMBL
Affinity DataKi: 7.00E+5nMAssay Description:Inhibition of Escherichia coli DHDPSMore data for this Ligand-Target Pair
Target4-hydroxy-tetrahydrodipicolinate synthase(Escherichia coli (strain K12))
University Of Melbourne
Curated by ChEMBL
University Of Melbourne
Curated by ChEMBL
Affinity DataKi: 8.30E+5nMAssay Description:Inhibition of Escherichia coli DHDPSMore data for this Ligand-Target Pair
Target4-hydroxy-tetrahydrodipicolinate synthase(Escherichia coli (strain K12))
University Of Melbourne
Curated by ChEMBL
University Of Melbourne
Curated by ChEMBL
Affinity DataKi: 1.63E+6nMAssay Description:Inhibition of Escherichia coli recombinant DHDPS overexpressed with DHDPR assessed as residual activity by modified coupled assayMore data for this Ligand-Target Pair
Target4-hydroxy-2-oxoglutarate aldolase, mitochondrial(Homo sapiens (Human))
University Of Melbourne
Curated by ChEMBL
University Of Melbourne
Curated by ChEMBL
Affinity DataKi: 2.96E+6nMAssay Description:Inhibition of dihydrodipicolinate synthaseMore data for this Ligand-Target Pair
Target4-hydroxy-tetrahydrodipicolinate synthase(Escherichia coli (strain K12))
University Of Melbourne
Curated by ChEMBL
University Of Melbourne
Curated by ChEMBL
Affinity DataKi: 4.95E+6nMAssay Description:Inhibition of Escherichia coli recombinant DHDPS overexpressed with DHDPR assessed as residual activity by modified coupled assayMore data for this Ligand-Target Pair
Target4-hydroxy-tetrahydrodipicolinate synthase(Escherichia coli (strain K12))
University Of Melbourne
Curated by ChEMBL
University Of Melbourne
Curated by ChEMBL
Affinity DataKi: 1.09E+7nMAssay Description:Inhibition of Escherichia coli recombinant DHDPS overexpressed with DHDPR assessed as residual activity by modified coupled assayMore data for this Ligand-Target Pair
Target4-hydroxy-2-oxoglutarate aldolase, mitochondrial(Homo sapiens (Human))
University Of Melbourne
Curated by ChEMBL
University Of Melbourne
Curated by ChEMBL
Affinity DataKi: 1.10E+7nMAssay Description:Inhibition of dihydrodipicolinate synthaseMore data for this Ligand-Target Pair
Target4-hydroxy-tetrahydrodipicolinate synthase(Escherichia coli (strain K12))
University Of Melbourne
Curated by ChEMBL
University Of Melbourne
Curated by ChEMBL
Affinity DataKi: 3.24E+7nMAssay Description:Inhibition of Escherichia coli recombinant DHDPS overexpressed with DHDPR assessed as residual activity by modified coupled assayMore data for this Ligand-Target Pair
TargetProteasome subunit beta type-8(Homo sapiens (Human))
The University Of Melbourne
Curated by ChEMBL
The University Of Melbourne
Curated by ChEMBL
Affinity DataIC50: 1.30nMAssay Description:Inhibition of human 20S immunoproteasome beta 5 subunit chymotrypsin-like activity using fluorogenic peptide Ac-WLA-AMC as substrate in presence of P...More data for this Ligand-Target Pair
TargetProteasome subunit beta type-5(Homo sapiens (Human))
The University Of Melbourne
Curated by ChEMBL
The University Of Melbourne
Curated by ChEMBL
Affinity DataIC50: 1.40nMAssay Description:Inhibition of human 20S constitutive proteasome beta 5 subunit chymotrypsin-like activity using fluorogenic peptide Ac-WLA-AMC as substrate in presen...More data for this Ligand-Target Pair