Compile Data Set for Download or QSAR
Found 33 Enz. Inhib. hit(s) with all data for entry = 50010621
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540648(CHEMBL4639944)copy SMILEScopy InChI
Affinity DataIC50: 0.100nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540643(CHEMBL4639941)copy SMILEScopy InChI
Affinity DataIC50: 0.130nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540639(CHEMBL4632810)copy SMILEScopy InChI
Affinity DataIC50: 0.130nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540640(CHEMBL4641768)copy SMILEScopy InChI
Affinity DataIC50: 0.140nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540649(CHEMBL4642214)copy SMILEScopy InChI
Affinity DataIC50: 0.160nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540655(CHEMBL4635889)copy SMILEScopy InChI
Affinity DataIC50: 0.170nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540642(CHEMBL4649085)copy SMILEScopy InChI
Affinity DataIC50: 0.180nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540644(CHEMBL4639413)copy SMILEScopy InChI
Affinity DataIC50: 0.190nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540638(CHEMBL4649563)copy SMILEScopy InChI
Affinity DataIC50: 0.200nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540645(CHEMBL4645937)copy SMILEScopy InChI
Affinity DataIC50: 0.210nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540646(CHEMBL4634153)copy SMILEScopy InChI
Affinity DataIC50: 0.25nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540654(CHEMBL4642738)copy SMILEScopy InChI
Affinity DataIC50: 0.270nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540653(CHEMBL4637660)copy SMILEScopy InChI
Affinity DataIC50: 0.280nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540641(CHEMBL4636234)copy SMILEScopy InChI
Affinity DataIC50: 0.300nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540651(CHEMBL4645131)copy SMILEScopy InChI
Affinity DataIC50: 0.340nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540652(CHEMBL4638582)copy SMILEScopy InChI
Affinity DataIC50: 0.340nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540647(CHEMBL4641915)copy SMILEScopy InChI
Affinity DataIC50: 0.380nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540650(CHEMBL4640188)copy SMILEScopy InChI
Affinity DataIC50: 0.600nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540656(CHEMBL4644376)copy SMILEScopy InChI
Affinity DataIC50: 1.02E+3nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540659(CHEMBL4646883)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+3nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540637(CHEMBL4647151)copy SMILEScopy InChI
Affinity DataIC50: 1.85E+3nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540657(CHEMBL4642447)copy SMILEScopy InChI
Affinity DataIC50: 2.26E+3nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540658(CHEMBL4648160)copy SMILEScopy InChI
Affinity DataIC50: 2.29E+3nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540660(CHEMBL4644683)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540636(CHEMBL4647625)copy SMILEScopy InChI
Affinity DataIC50: 1.97E+4nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50236398(CHEMBL1503273)copy SMILEScopy InChI
Affinity DataIC50: 2.57E+4nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540662(CHEMBL4639754)copy SMILEScopy InChI
Affinity DataIC50: 3.04E+4nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540663(CHEMBL4646647)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540664(CHEMBL4643702)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540665(CHEMBL4647974)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540666(CHEMBL4641231)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540667(CHEMBL4639402)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology IRCCS

Curated by ChEMBL
LigandPNGBDBM50540661(CHEMBL4639446)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using biotinylated H3K4me as substrate by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6GFNPubMed