BDBM50572574 CHEMBL4863608
SMILES Cc1ccc(cc1)-c1cc2occ(CN3CCC[C@H](N)C3)c2cc1-c1ccc(cc1)C#N
InChI Key InChIKey=MQEXBLBDOHQHHG-UHFFFAOYSA-N
Data 7 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 7 hits for monomerid = 50572574
TargetLysine-specific histone demethylase 1A(Human)
Shenyang Pharmaceutical University
Curated by ChEMBL
Shenyang Pharmaceutical University
Curated by ChEMBL
Affinity DataIC50: 61nMAssay Description:Inhibition of human recombinant LSD1 by horseradish peroxidase-coupled fluorometric assayMore data for this Ligand-Target Pair
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of N-terminal FLAG-tagged human recombinant MAO-A expressed in baculovirus-infected Sf9 cells by flow cytometryMore data for this Ligand-Target Pair
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of N-terminal FLAG-tagged human recombinant MAO-B expressed in baculovirus-infected Sf9 cells by flow cytometryMore data for this Ligand-Target Pair
TargetLysine-specific histone demethylase 1A(Human)
Shenyang Pharmaceutical University
Curated by ChEMBL
Shenyang Pharmaceutical University
Curated by ChEMBL
Affinity DataIC50: 65nMAssay Description:Inhibition of recombinant human LSD1 using fluorometric substrate by HRP based fluorimeter microplate reader assayMore data for this Ligand-Target Pair
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of recombinant MAO-A (unknown origin) incubated for 60 mins by luminescence based flow cytometryMore data for this Ligand-Target Pair
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of recombinant MAO-B (unknown origin) incubated for 60 mins by luminescence based flow cytometryMore data for this Ligand-Target Pair
TargetLysine-specific histone demethylase 1A(Human)
Shenyang Pharmaceutical University
Curated by ChEMBL
Shenyang Pharmaceutical University
Curated by ChEMBL
Affinity DataIC50: 65nMAssay Description:Inhibition of LSD1 (unknown origin)More data for this Ligand-Target Pair