Compile Data Set for Download or QSAR
maximum 50k data
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)
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 ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology Irccs

Curated by ChEMBL
LigandPNGBDBM50540643(CHEMBL4639941)
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 ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology Irccs

Curated by ChEMBL
LigandPNGBDBM50540639(CHEMBL4632810)
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 ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology Irccs

Curated by ChEMBL
LigandPNGBDBM50540640(CHEMBL4641768)
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 ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology Irccs

Curated by ChEMBL
LigandPNGBDBM50540649(CHEMBL4642214)
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 ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology Irccs

Curated by ChEMBL
LigandPNGBDBM50540655(CHEMBL4635889)
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 ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology Irccs

Curated by ChEMBL
LigandPNGBDBM50540642(CHEMBL4649085)
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 ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology Irccs

Curated by ChEMBL
LigandPNGBDBM50540644(CHEMBL4639413)
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)
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 ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology Irccs

Curated by ChEMBL
LigandPNGBDBM50540645(CHEMBL4645937)
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 ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology Irccs

Curated by ChEMBL
LigandPNGBDBM50540646(CHEMBL4634153)
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 ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology Irccs

Curated by ChEMBL
LigandPNGBDBM50540654(CHEMBL4642738)
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 ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology Irccs

Curated by ChEMBL
LigandPNGBDBM50540653(CHEMBL4637660)
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 ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology Irccs

Curated by ChEMBL
LigandPNGBDBM50540641(CHEMBL4636234)
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 ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology Irccs

Curated by ChEMBL
LigandPNGBDBM50540651(CHEMBL4645131)
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 ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology Irccs

Curated by ChEMBL
LigandPNGBDBM50540652(CHEMBL4638582)
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 ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology Irccs

Curated by ChEMBL
LigandPNGBDBM50540647(CHEMBL4641915)
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 ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology Irccs

Curated by ChEMBL
LigandPNGBDBM50540650(CHEMBL4640188)
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 ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology Irccs

Curated by ChEMBL
LigandPNGBDBM50540656(CHEMBL4644376)
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 ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology Irccs

Curated by ChEMBL
LigandPNGBDBM50540659(CHEMBL4646883)
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 ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology Irccs

Curated by ChEMBL
LigandPNGBDBM50540637(CHEMBL4647151)
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 ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology Irccs

Curated by ChEMBL
LigandPNGBDBM50540657(CHEMBL4642447)
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 ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology Irccs

Curated by ChEMBL
LigandPNGBDBM50540658(CHEMBL4648160)
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 ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology Irccs

Curated by ChEMBL
LigandPNGBDBM50540660(CHEMBL4644683)
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 ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology Irccs

Curated by ChEMBL
LigandPNGBDBM50540636(CHEMBL4647625)
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 ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology Irccs

Curated by ChEMBL
LigandPNGBDBM50236398(CHEMBL1503273)
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 ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology Irccs

Curated by ChEMBL
LigandPNGBDBM50540662(CHEMBL4639754)
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 ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology Irccs

Curated by ChEMBL
LigandPNGBDBM50540663(CHEMBL4646647)
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 ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology Irccs

Curated by ChEMBL
LigandPNGBDBM50540664(CHEMBL4643702)
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 ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology Irccs

Curated by ChEMBL
LigandPNGBDBM50540665(CHEMBL4647974)
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 ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology Irccs

Curated by ChEMBL
LigandPNGBDBM50540666(CHEMBL4641231)
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 ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology Irccs

Curated by ChEMBL
LigandPNGBDBM50540667(CHEMBL4639402)
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 ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
European Institute of Oncology Irccs

Curated by ChEMBL
LigandPNGBDBM50540661(CHEMBL4639446)
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 ArticlePubMed