Compile Data Set for Download or QSAR

Found 51 hits of Enzyme Inhibition Constant Data   

TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517684(CHEMBL4569986)copy SMILEScopy InChI
Affinity DataIC50: 61nMAssay Description:Inhibition of recombinant human LSD1 (172 to 852 residues) using biotin-labelled H3K4me2 (1 to 24 residues) after 1 hr by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517680(CHEMBL4533143)copy SMILEScopy InChI
Affinity DataIC50: 66nMAssay Description:Inhibition of recombinant human LSD1 (172 to 852 residues) using biotin-labelled H3K4me2 (1 to 24 residues) after 1 hr by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517676(CHEMBL4580675)copy SMILEScopy InChI
Affinity DataIC50: 84nMAssay Description:Inhibition of recombinant human LSD1 (172 to 852 residues) using biotin-labelled H3K4me2 (1 to 24 residues) after 1 hr by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517682(CHEMBL4520948)copy SMILEScopy InChI
Affinity DataIC50: 109nMAssay Description:Inhibition of recombinant human LSD1 (172 to 852 residues) using biotin-labelled H3K4me2 (1 to 24 residues) after 1 hr by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517678(CHEMBL4437554)copy SMILEScopy InChI
Affinity DataIC50: 124nMAssay Description:Inhibition of recombinant human LSD1 (172 to 852 residues) using biotin-labelled H3K4me2 (1 to 24 residues) after 1 hr by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517686(CHEMBL4589914)copy SMILEScopy InChI
Affinity DataIC50: 146nMAssay Description:Inhibition of recombinant human LSD1 (172 to 852 residues) using biotin-labelled H3K4me2 (1 to 24 residues) after 1 hr by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517683(CHEMBL4550942)copy SMILEScopy InChI
Affinity DataIC50: 184nMAssay Description:Inhibition of recombinant human LSD1 (172 to 852 residues) using biotin-labelled H3K4me2 (1 to 24 residues) after 1 hr by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517685(CHEMBL4447074)copy SMILEScopy InChI
Affinity DataIC50: 187nMAssay Description:Inhibition of recombinant human LSD1 (172 to 852 residues) using biotin-labelled H3K4me2 (1 to 24 residues) after 1 hr by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517681(CHEMBL4442317)copy SMILEScopy InChI
Affinity DataIC50: 211nMAssay Description:Inhibition of recombinant human LSD1 (172 to 852 residues) using biotin-labelled H3K4me2 (1 to 24 residues) after 1 hr by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517675(CHEMBL4440500)copy SMILEScopy InChI
Affinity DataIC50: 241nMAssay Description:Inhibition of recombinant human LSD1 (172 to 852 residues) using biotin-labelled H3K4me2 (1 to 24 residues) after 1 hr by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517679(CHEMBL4530202)copy SMILEScopy InChI
Affinity DataIC50: 242nMAssay Description:Inhibition of recombinant human LSD1 (172 to 852 residues) using biotin-labelled H3K4me2 (1 to 24 residues) after 1 hr by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517673(CHEMBL4593261)copy SMILEScopy InChI
Affinity DataIC50: 252nMAssay Description:Inhibition of recombinant human LSD1 (172 to 852 residues) using biotin-labelled H3K4me2 (1 to 24 residues) after 1 hr by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517677(CHEMBL4474185)copy SMILEScopy InChI
Affinity DataIC50: 303nMAssay Description:Inhibition of recombinant human LSD1 (172 to 852 residues) using biotin-labelled H3K4me2 (1 to 24 residues) after 1 hr by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517674(CHEMBL4558443)copy SMILEScopy InChI
Affinity DataIC50: 360nMAssay Description:Inhibition of recombinant human LSD1 (172 to 852 residues) using biotin-labelled H3K4me2 (1 to 24 residues) after 1 hr by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50240772((1R,2S)-(-)-2-phenylcyclopropylamine | (1R,2S)-2-p...)copy SMILEScopy InChI
Affinity DataIC50: 560nMAssay Description:Inhibition of MAOB (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517687(CHEMBL4526830)copy SMILEScopy InChI
Affinity DataIC50: 692nMAssay Description:Inhibition of recombinant human LSD1 (172 to 852 residues) using biotin-labelled H3K4me2 (1 to 24 residues) after 1 hr by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50240772((1R,2S)-(-)-2-phenylcyclopropylamine | (1R,2S)-2-p...)copy SMILEScopy InChI
Affinity DataIC50: 1.02E+3nMAssay Description:Inhibition of MAOA (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517676(CHEMBL4580675)copy SMILEScopy InChI
Affinity DataIC50: 1.16E+3nMAssay Description:Inhibition of MAOB (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50158869(CHEMBL3786182 | US10836743, Compound GSK-2879552 |...)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibition of recombinant human LSD1 (172 to 852 residues) using biotin-labelled H3K4me2 (1 to 24 residues) after 1 hr by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517680(CHEMBL4533143)copy SMILEScopy InChI
Affinity DataIC50: 1.21E+3nMAssay Description:Inhibition of MAOB (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517676(CHEMBL4580675)copy SMILEScopy InChI
Affinity DataIC50: 2.23E+3nMAssay Description:Inhibition of MAOA (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517682(CHEMBL4520948)copy SMILEScopy InChI
Affinity DataIC50: 4.10E+3nMAssay Description:Inhibition of MAOA (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517678(CHEMBL4437554)copy SMILEScopy InChI
Affinity DataIC50: 4.55E+3nMAssay Description:Inhibition of MAOA (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517682(CHEMBL4520948)copy SMILEScopy InChI
Affinity DataIC50: 4.81E+3nMAssay Description:Inhibition of MAOB (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517678(CHEMBL4437554)copy SMILEScopy InChI
Affinity DataIC50: 6.05E+3nMAssay Description:Inhibition of MAOB (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517687(CHEMBL4526830)copy SMILEScopy InChI
Affinity DataIC50: 8.27E+3nMAssay Description:Inhibition of MAOA (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517683(CHEMBL4550942)copy SMILEScopy InChI
Affinity DataIC50: 8.57E+3nMAssay Description:Inhibition of MAOA (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517684(CHEMBL4569986)copy SMILEScopy InChI
Affinity DataIC50: 9.19E+3nMAssay Description:Inhibition of MAOA (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517684(CHEMBL4569986)copy SMILEScopy InChI
Affinity DataIC50: 9.63E+3nMAssay Description:Inhibition of MAOB (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517681(CHEMBL4442317)copy SMILEScopy InChI
Affinity DataIC50: 1.25E+4nMAssay Description:Inhibition of MAOA (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517685(CHEMBL4447074)copy SMILEScopy InChI
Affinity DataIC50: 1.29E+4nMAssay Description:Inhibition of MAOA (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517674(CHEMBL4558443)copy SMILEScopy InChI
Affinity DataIC50: 2.04E+4nMAssay Description:Inhibition of MAOB (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517673(CHEMBL4593261)copy SMILEScopy InChI
Affinity DataIC50: 2.08E+4nMAssay Description:Inhibition of MAOA (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517674(CHEMBL4558443)copy SMILEScopy InChI
Affinity DataIC50: 2.10E+4nMAssay Description:Inhibition of MAOA (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50240772((1R,2S)-(-)-2-phenylcyclopropylamine | (1R,2S)-2-p...)copy SMILEScopy InChI
Affinity DataIC50: 2.19E+4nMAssay Description:Inhibition of recombinant human LSD1 (172 to 852 residues) using biotin-labelled H3K4me2 (1 to 24 residues) after 1 hr by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517683(CHEMBL4550942)copy SMILEScopy InChI
Affinity DataIC50: 2.20E+4nMAssay Description:Inhibition of MAOB (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517685(CHEMBL4447074)copy SMILEScopy InChI
Affinity DataIC50: 2.88E+4nMAssay Description:Inhibition of MAOB (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517687(CHEMBL4526830)copy SMILEScopy InChI
Affinity DataIC50: 3.67E+4nMAssay Description:Inhibition of MAOB (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517681(CHEMBL4442317)copy SMILEScopy InChI
Affinity DataIC50: 4.03E+4nMAssay Description:Inhibition of MAOB (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517680(CHEMBL4533143)copy SMILEScopy InChI
Affinity DataIC50: 4.09E+4nMAssay Description:Inhibition of MAOA (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517686(CHEMBL4589914)copy SMILEScopy InChI
Affinity DataIC50: 4.75E+4nMAssay Description:Inhibition of MAOA (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517673(CHEMBL4593261)copy SMILEScopy InChI
Affinity DataIC50: 4.95E+4nMAssay Description:Inhibition of MAOB (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517675(CHEMBL4440500)copy SMILEScopy InChI
Affinity DataIC50: 5.64E+4nMAssay Description:Inhibition of MAOA (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517677(CHEMBL4474185)copy SMILEScopy InChI
Affinity DataIC50: 6.59E+4nMAssay Description:Inhibition of MAOA (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517686(CHEMBL4589914)copy SMILEScopy InChI
Affinity DataIC50: 7.16E+4nMAssay Description:Inhibition of MAOB (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517679(CHEMBL4530202)copy SMILEScopy InChI
Affinity DataIC50: 7.56E+4nMAssay Description:Inhibition of MAOB (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517675(CHEMBL4440500)copy SMILEScopy InChI
Affinity DataIC50: 9.56E+4nMAssay Description:Inhibition of MAOB (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50158869(CHEMBL3786182 | US10836743, Compound GSK-2879552 |...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of MAOA (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50517679(CHEMBL4530202)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of MAOA (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Liaoning Shihua University

Curated by ChEMBL
LigandPNGBDBM50158869(CHEMBL3786182 | US10836743, Compound GSK-2879552 |...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of MAOB (unknown origin) by Promega MAO-Glo assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2TB1PubMed
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