BDBM50568522 CHEMBL4864352
SMILES CN1CCN(CC1)C(=O)CNC1CC1c1cc(F)cc(F)c1OCc1ccccc1
InChI Key InChIKey=GNKCLVXPAGTZSF-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 11 hits for monomerid = 50568522
TargetLysine-specific histone demethylase 1A(Human)
Riken Center For Sustainable Resource Science
Curated by ChEMBL
Riken Center For Sustainable Resource Science
Curated by ChEMBL
Affinity DataIC50: 870nMAssay Description:Inhibition of human LSD1 assessed as demethylase activity of LSD1 using Histone H3(1-20)K4me2 peptide as substrate incubated for 10 mins followed by ...More data for this Ligand-Target Pair
TargetLysine-specific histone demethylase 1A(Human)
Riken Center For Sustainable Resource Science
Curated by ChEMBL
Riken Center For Sustainable Resource Science
Curated by ChEMBL
Affinity DataIC50: 870nMAssay Description:Inhibition of LSD1 (unknown origin)More data for this Ligand-Target Pair
TargetLysine-specific histone demethylase 1A(Human)
Riken Center For Sustainable Resource Science
Curated by ChEMBL
Riken Center For Sustainable Resource Science
Curated by ChEMBL
Affinity DataKi: 370nMAssay Description:Inhibition of human LSD1 (172 to 833 residues) using Lys4-dimethylated H3 (1-20) peptide as substrate incubated for 30 mins by peroxidase-coupled ass...More data for this Ligand-Target Pair
TargetLysine-specific histone demethylase 1A(Human)
Riken Center For Sustainable Resource Science
Curated by ChEMBL
Riken Center For Sustainable Resource Science
Curated by ChEMBL
Affinity DataKi: 370nMAssay Description:Inhibition of LSD1 (unknown origin) assessed as inhibition constant by peroxidase-coupled assayMore data for this Ligand-Target Pair
TargetLysine-specific histone demethylase 1A(Human)
Riken Center For Sustainable Resource Science
Curated by ChEMBL
Riken Center For Sustainable Resource Science
Curated by ChEMBL
Affinity DataKi: 750nMAssay Description:Inhibition of human LSD1 assessed as inhibitory constant using Histone H3(1-20)K4me2 peptide as substrate incubated for 10 mins followed by substrate...More data for this Ligand-Target Pair
Affinity DataKi: >2.50E+5nMAssay Description:Inhibition of LSD2 (unknown origin) using Lys4-dimethylated H3 (1-20) peptide as substrate incubated for 30 mins by peroxidase-coupled assayMore data for this Ligand-Target Pair
Affinity DataKi: >2.50E+5nMAssay Description:Inhibition of human MAO-A expressed in baculovirus infected BTI insect cells using tyramine as substrate incubated for 30 mins by peroxidase-coupled ...More data for this Ligand-Target Pair
Affinity DataKi: >2.50E+5nMAssay Description:Inhibition of human MAO-B expressed in expressed in baculovirus infected BTI insect cells using tyramine as substrate incubated for 30 mins by fluore...More data for this Ligand-Target Pair
Affinity DataKi: >2.50E+5nMAssay Description:Inhibition of MAO-A (unknown origin) assessed as inhibition constantMore data for this Ligand-Target Pair
Affinity DataKi: >2.50E+5nMAssay Description:Inhibition of LSD2 (unknown origin) assessed as inhibition constantMore data for this Ligand-Target Pair
Affinity DataKi: >2.50E+5nMAssay Description:Inhibition of MAO-B (unknown origin) assessed as inhibition constantMore data for this Ligand-Target Pair