Found 137 Enz. Inhib. hit(s) with Target = 'Aldehyde dehydrogenase family 1 member A3' TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataKi: 120nMAssay Description:Competitive inhibition of human recombinant ALDH1A3 pre-incubated for 5 mins before acetaldehyde addition by continuous spectrometric assay relative ...More data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataKi: 261nMAssay Description:Inhibition of human ALDH1A3More data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataKi: 460nMAssay Description:Competitive inhibition of N-terminal-His6 tagged recombinant human ALDH1A3 assessed as increase in Km without change in Vmax using hexanal as substra...More data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataKi: 540nMAssay Description:Competitive inhibition of recombinant human 6His-tagged ALDH1A3 expressed in Escherichia coli BL21(DE3) using varying level of acetaldehyde as substr...More data for this Ligand-Target Pair
3D Structure (crystal)TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataKi: <1.00E+3nMAssay Description:Competitive inhibition of N-terminal-His6 tagged recombinant human ALDH1A3 assessed as increase in Km without change in Vmax using hexanal as substra...More data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataKi: <1.00E+3nMAssay Description:Competitive inhibition of N-terminal-His6 tagged recombinant human ALDH1A3 assessed as increase in Km without change in Vmax using hexanal as substra...More data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataKi: 8.70E+3nMAssay Description:Competitive inhibition of human recombinant ALDH1A3 pre-incubated for 5 mins before acetaldehyde addition by continuous spectrometric assay relative ...More data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: 34nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: 50nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: 60nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: 73nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: 89nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: 90nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: 90nMAssay Description:Inhibition of human recombinant ALDH1A3 assessed as reduction in of NAD(P)H formation incubated for 2 mins by spectrophotometryMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: 91nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: 95nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: <100nMAssay Description:In vitro inhibition of human dihydrofolate reductaseMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: 100nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: <100nMAssay Description:Inhibition of dihydrofolate reductase in Candida albicans (in vitro).More data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: <100nMAssay Description:In vitro inhibition of human dihydrofolate reductaseMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: <100nMAssay Description:In vitro inhibition of human dihydrofolate reductaseMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: <100nMAssay Description:Inhibition of dihydrofolate reductase in Candida albicans (in vitro).More data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: <100nMAssay Description:Inhibition of dihydrofolate reductase in Candida albicans (in vitro).More data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: <100nMAssay Description:Inhibition of dihydrofolate reductase in Candida albicans (in vitro).More data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: <100nMAssay Description:Inhibition of dihydrofolate reductase in Candida albicans (in vitro).More data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: <100nMAssay Description:In vitro inhibition of human dihydrofolate reductaseMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: <100nMAssay Description:Potency against histamine H1 receptor on guinea pig ileumMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: <100nMAssay Description:Potency against histamine H1 receptor on guinea pig ileumMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: <100nMAssay Description:Potency against histamine H1 receptor on guinea pig ileumMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: <100nMAssay Description:Potency against histamine H1 receptor on guinea pig ileumMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: <100nMAssay Description:Potency against histamine H1 receptor on guinea pig ileumMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: <100nMAssay Description:Inhibition of squalene synthaseMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: <100nMAssay Description:Inhibition of mevalonate kinaseMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: 109nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: 112nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: 119nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: 120nMAssay Description:Inhibition of human recombinant ALDH1A3 assessed as reduction in of NAD(P)H formation incubated for 2 mins by spectrophotometryMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: 120nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: 128nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: 130nMAssay Description:Inhibition of human recombinant ALDH1A3 assessed as reduction in of NAD(P)H formation incubated for 2 mins by spectrophotometryMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: 130nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: 130nMAssay Description:Inhibition of human recombinant ALDH1A3 assessed as reduction in of NAD(P)H formation incubated for 2 mins by spectrophotometryMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: 140nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: 150nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: 170nMAssay Description:Inhibition of full length recombinant human ALDH1A3 expressed in Escherichia coli BL21(DE3) assessed as reduction in dehydrogenase activity by measur...More data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: 170nMAssay Description:Inhibition of human recombinant ALDH1A3 assessed as reduction in of NAD(P)H formation incubated for 2 mins by spectrophotometryMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: 170nMAssay Description:Inhibition of human recombinant ALDH1A3 assessed as reduction in of NAD(P)H formation incubated for 2 mins by spectrophotometryMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: 174nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
Affinity DataIC50: 180nMAssay Description:Inhibition of human recombinant ALDH1A3 assessed as reduction in of NAD(P)H formation incubated for 2 mins by spectrophotometryMore data for this Ligand-Target Pair
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University Of Pisa
Curated by ChEMBL
University Of Pisa
Curated by ChEMBL
