Compile Data Set for Download or QSAR
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
LigandPNGBDBM50538688(CHEMBL4642789)copy SMILEScopy InChI
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
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N301G7PubMed
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50459608(CHEBI:90441 | CHEMBL3276621)copy SMILEScopy InChI
Affinity DataKi:  261nMAssay Description:Inhibition of human ALDH1A3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V127F6PubMed
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50585949(CHEMBL5083058)copy SMILES
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
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22Z19FTPubMed
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50527781(CHEMBL4456676)copy SMILEScopy InChI
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
Ligand InfoPC cidPC sidPDB
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50585950(CHEMBL5075900)copy SMILES
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
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22Z19FTPubMed
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50585951(CHEMBL5086460)copy SMILES
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
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22Z19FTPubMed
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50538685(CHEMBL4644541)copy SMILEScopy InChI
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
Ligand InfoPC cidPC sidPDB
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50567363(CHEMBL4876602)copy SMILES
Affinity DataIC50: 34nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58R5MPubMed
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50567386(CHEMBL4861872)copy SMILES
Affinity DataIC50: 50nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58R5MPubMed
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50567382(CHEMBL4859904)copy SMILES
Affinity DataIC50: 60nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58R5MPubMed
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50567362(CHEMBL4848258)copy SMILES
Affinity DataIC50: 73nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58R5MPubMed
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50567372(CHEMBL4875157)copy SMILES
Affinity DataIC50: 89nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58R5MPubMed
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50459603(CHEMBL4213331)copy SMILEScopy InChI
Affinity DataIC50: 90nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58R5MPubMed
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50459603(CHEMBL4213331)copy SMILEScopy InChI
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
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V127F6PubMed
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50567376(CHEMBL4848831)copy SMILES
Affinity DataIC50: 91nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58R5MPubMed
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50567373(CHEMBL4855442)copy SMILES
Affinity DataIC50: 95nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58R5MPubMed
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50406337(CHEMBL5271934)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:In vitro inhibition of human dihydrofolate reductaseMore data for this Ligand-Target Pair
In DepthDetails
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50567374(CHEMBL4849624)copy SMILES
Affinity DataIC50: 100nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58R5MPubMed
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50406343(CHEMBL5269320)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Inhibition of dihydrofolate reductase in Candida albicans (in vitro).More data for this Ligand-Target Pair
In DepthDetails
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50406342(CHEMBL5283146)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:In vitro inhibition of human dihydrofolate reductaseMore data for this Ligand-Target Pair
In DepthDetails
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50406341(CHEMBL5291299)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:In vitro inhibition of human dihydrofolate reductaseMore data for this Ligand-Target Pair
In DepthDetails
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50406340(CHEMBL5286018)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Inhibition of dihydrofolate reductase in Candida albicans (in vitro).More data for this Ligand-Target Pair
In DepthDetails
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50406339(CHEMBL5278448)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Inhibition of dihydrofolate reductase in Candida albicans (in vitro).More data for this Ligand-Target Pair
In DepthDetails
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50406338(CHEMBL5274968)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Inhibition of dihydrofolate reductase in Candida albicans (in vitro).More data for this Ligand-Target Pair
In DepthDetails
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50406336(CHEMBL5285815)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Inhibition of dihydrofolate reductase in Candida albicans (in vitro).More data for this Ligand-Target Pair
In DepthDetails
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50406343(CHEMBL5269320)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:In vitro inhibition of human dihydrofolate reductaseMore data for this Ligand-Target Pair
In DepthDetails
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50406342(CHEMBL5283146)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Potency against histamine H1 receptor on guinea pig ileumMore data for this Ligand-Target Pair
In DepthDetails
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50406341(CHEMBL5291299)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Potency against histamine H1 receptor on guinea pig ileumMore data for this Ligand-Target Pair
In DepthDetails
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50406340(CHEMBL5286018)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Potency against histamine H1 receptor on guinea pig ileumMore data for this Ligand-Target Pair
In DepthDetails
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50406339(CHEMBL5278448)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Potency against histamine H1 receptor on guinea pig ileumMore data for this Ligand-Target Pair
In DepthDetails
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50406338(CHEMBL5274968)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Potency against histamine H1 receptor on guinea pig ileumMore data for this Ligand-Target Pair
In DepthDetails
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50406337(CHEMBL5271934)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Inhibition of squalene synthaseMore data for this Ligand-Target Pair
In DepthDetails
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50406336(CHEMBL5285815)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Inhibition of mevalonate kinaseMore data for this Ligand-Target Pair
In DepthDetails
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50567383(CHEMBL4847114)copy SMILES
Affinity DataIC50: 109nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58R5MPubMed
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50567377(CHEMBL4874309)copy SMILES
Affinity DataIC50: 112nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58R5MPubMed
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50567366(CHEMBL4876076)copy SMILES
Affinity DataIC50: 119nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58R5MPubMed
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50459588(CHEMBL4210115)copy SMILEScopy InChI
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
Ligand InfoPC cidPC sidPDB
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V127F6PubMed
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50459588(CHEMBL4210115)copy SMILEScopy InChI
Affinity DataIC50: 120nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58R5MPubMed
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50567361(CHEMBL4862833)copy SMILES
Affinity DataIC50: 128nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58R5MPubMed
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50459613(CHEMBL4214509)copy SMILEScopy InChI
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
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V127F6PubMed
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50567367(CHEMBL4863668)copy SMILES
Affinity DataIC50: 130nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58R5MPubMed
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50459593(CHEMBL4217452)copy SMILEScopy InChI
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
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V127F6PubMed
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50567352(CHEMBL4873315)copy SMILES
Affinity DataIC50: 140nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58R5MPubMed
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50567369(CHEMBL4873090)copy SMILES
Affinity DataIC50: 150nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58R5MPubMed
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50236905(CHEMBL1349972)copy SMILEScopy InChI
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
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32Z11PubMed
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50459602(CHEMBL4216790)copy SMILEScopy InChI
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
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V127F6PubMed
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50459612(CHEMBL4205216)copy SMILEScopy InChI
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
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V127F6PubMed
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50567378(CHEMBL4846491)copy SMILES
Affinity DataIC50: 174nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58R5MPubMed
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50459599(CHEMBL4213859)copy SMILEScopy InChI
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
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V127F6PubMed
TargetAldehyde dehydrogenase family 1 member A3(Homo sapiens (Human))
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50459608(CHEBI:90441 | CHEMBL3276621)copy SMILEScopy InChI
Affinity DataIC50: 187nMMore data for this Ligand-Target Pair
In DepthDetails
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