Compile Data Set for Download or QSAR
Report error Found 15 Enz. Inhib. hit(s) with all data for entry = 50011495
TargetREST corepressor 1(Human)
Taipei Medical University

Curated by ChEMBL
LigandPNGBDBM50507295(CHEMBL1232432)
Affinity DataKd:  243nMAssay Description:Binding affinity to LSD1/CoREST (unknown origin) expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails Article
PubMedPDB3D3D Structure (crystal)
TargetREST corepressor 1(Human)
Taipei Medical University

Curated by ChEMBL
LigandPNGBDBM50548037(CHEMBL2397513)
Affinity DataKd:  463nMAssay Description:Binding affinity to LSD1/CoREST (unknown origin) expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetREST corepressor 1(Human)
Taipei Medical University

Curated by ChEMBL
LigandPNGBDBM50548038(CHEMBL3781027)
Affinity DataKd:  594nMAssay Description:Binding affinity to LSD1/CoREST (unknown origin) expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetLysine-specific histone demethylase 1A(Human)
Taipei Medical University

Curated by ChEMBL
LigandPNGBDBM179446(US9676701, 4 4′-((trans)-2-aminocyclopropyl)...)
Affinity DataIC50: 20nMAssay Description:Inhibition of human recombinant LSD1 (158 to end residues) expressed in Escherichia coli using dimethylated H3K4 peptide as substrate by horseradish ...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetLysine-specific histone demethylase 1A(Human)
Taipei Medical University

Curated by ChEMBL
LigandPNGBDBM50548033(CHEMBL4743670)
Affinity DataIC50: 29nMAssay Description:Inhibition of human recombinant LSD1 using ARTK(diMe)QTARKSTGGKAPRKQLA as substrate incubated for 30 mins by fluorometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetLysine-specific histone demethylase 1A(Human)
Taipei Medical University

Curated by ChEMBL
LigandPNGBDBM50548035(CHEMBL4740695)
Affinity DataIC50: 49nMAssay Description:Inhibition of LSD1 (unknown origin) expressed in Escherichia coli BL21(DE) cells using H3K4me2 as substrate incubated for 30 mins by horseradish pero...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetHistone deacetylase 1(Human)
Taipei Medical University

Curated by ChEMBL
LigandPNGBDBM50548040(CHEMBL4791172)
Affinity DataIC50: 147nMAssay Description:Inhibition of C-terminal His/FLAG-tagged human HDAC1 expressed in Sf9 insect cells using acetylated P53(379-382 residues) (RHKK(Ac)) as substrate inc...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetREST corepressor 1(Human)
Taipei Medical University

Curated by ChEMBL
LigandPNGBDBM50548040(CHEMBL4791172)
Affinity DataIC50: 330nMAssay Description:Inhibition of LSD1/FLAG-tagged CoREST (unknown origin) expressed in HEK293F cells using diMeK4H3(1 to 21 residues) as substrate preincubated for 5 mi...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetLysine-specific histone demethylase 1A(Human)
Taipei Medical University

Curated by ChEMBL
LigandPNGBDBM50548034(CHEMBL4785447)
Affinity DataIC50: 340nMAssay Description:Inhibition of LSD1 (unknown origin) (157 to 852 residues) expressed in Escherichia coli BL21(DE) cells using H3K4me2 as substrate by horseradish pero...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetLysine-specific histone demethylase 1A(Human)
Taipei Medical University

Curated by ChEMBL
LigandPNGBDBM50075474(CHEMBL3415352)
Affinity DataIC50: 650nMAssay Description:Inhibition of LSD1 (unknown origin) (157 to 852 residues) expressed in Escherichia coli BL21(DE) cells using H3K4me2 as substrate by horseradish pero...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetLysine-specific histone demethylase 1A(Human)
Taipei Medical University

Curated by ChEMBL
LigandPNGBDBM50242173((2S,3S,4S,5R,6S)-6-(5,6-dihydroxy-4-oxo-2-phenyl-4...)
Affinity DataIC50: 3.01E+3nMAssay Description:Inhibition of LSD1 (unknown origin) expressed in human MGC-803 cells incubated for 5 days by DAPI staining based immunofluorescence methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetLysine-specific histone demethylase 1A(Human)
Taipei Medical University

Curated by ChEMBL
LigandPNGBDBM50548036(CHEMBL4746827)
Affinity DataIC50: 4.00E+3nMAssay Description:Inhibition of human LSD1 (158 to end residues) expressed in Escherichia coli preincubated for 15 mins followed by H3K4me2 peptide addition and measur...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetLysine-specific histone demethylase 1A(Human)
Taipei Medical University

Curated by ChEMBL
LigandPNGBDBM225267(2-((5-Chloro-2-hydroxyphenyl)amino)-N-(3-(morpholi...)
Affinity DataIC50: 6.90E+3nMAssay Description:Inhibition of human LSD1 (158 to end residues) expressed in Escherichia coli preincubated for 15 mins followed by H3K4me2 peptide addition and measur...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetLysine-specific histone demethylase 1A(Human)
Taipei Medical University

Curated by ChEMBL
LigandPNGBDBM225266(2-((5-Chloro-2-hydroxyphenyl)(methyl)amino)-N-(3-(...)
Affinity DataIC50: 9.50E+3nMAssay Description:Inhibition of human LSD1 (158 to end residues) expressed in Escherichia coli preincubated for 15 mins followed by H3K4me2 peptide addition and measur...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetLysine-specific histone demethylase 1A(Human)
Taipei Medical University

Curated by ChEMBL
LigandPNGBDBM50548039(CHEMBL4798513)
Affinity DataKi:  2.20E+3nMAssay Description:Inhibition of human LSD1 preincubated for 10 mins followed by H3(1-20)K4-dimethylated (K4me2) peptide substrate addition and measured after 30 mins b...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed