BDBM50142080 CHEMBL3758211

SMILES: N#Cc1ccc(cc1)-c1cc(OCC2CCNCC2)cnc1-c1ccccc1

InChI Key: InChIKey=JRZAMLMCCFHWNL-UHFFFAOYSA-N

Data: 4 KI

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50142080   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50142080 (CHEMBL3758211) Show SMILES N#Cc1ccc(cc1)-c1cc(OCC2CCNCC2)cnc1-c1ccccc1 Show InChI InChI=1S/C24H23N3O/c25-15-18-6-8-20(9-7-18)23-14-22(28-17-19-10-12-26-13-11-19)16-27-24(23)21-4-2-1-3-5-21/h1-9,14,16,19,26H,10-13,17H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	1.80E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Baylor College of Medicine Curated by ChEMBL					Assay Description Competitive inhibition of recombinant human GST-tagged LSD1 catalytic domain (172 to 833 residues) using 2 to 100 uM dimethylated H3K4 peptide substr...				J Med Chem 59: 253-63 (2016) BindingDB Entry DOI: 10.7270/Q23J3FSW
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50142080 (CHEMBL3758211) Show SMILES N#Cc1ccc(cc1)-c1cc(OCC2CCNCC2)cnc1-c1ccccc1 Show InChI InChI=1S/C24H23N3O/c25-15-18-6-8-20(9-7-18)23-14-22(28-17-19-10-12-26-13-11-19)16-27-24(23)21-4-2-1-3-5-21/h1-9,14,16,19,26H,10-13,17H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	2.30E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Baylor College of Medicine Curated by ChEMBL					Assay Description Inhibition of recombinant human GST-tagged LSD1 catalytic domain (172 to 833 residues) using dimethylated H3K4 peptide substrate preincubated for 10 ...				J Med Chem 59: 253-63 (2016) BindingDB Entry DOI: 10.7270/Q23J3FSW
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] B (Homo sapiens (Human))	BDBM50142080 (CHEMBL3758211) Show SMILES N#Cc1ccc(cc1)-c1cc(OCC2CCNCC2)cnc1-c1ccccc1 Show InChI InChI=1S/C24H23N3O/c25-15-18-6-8-20(9-7-18)23-14-22(28-17-19-10-12-26-13-11-19)16-27-24(23)21-4-2-1-3-5-21/h1-9,14,16,19,26H,10-13,17H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	1.06E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Baylor College of Medicine Curated by ChEMBL					Assay Description Inhibition of recombinant human MAO-B after 60 mins MAO-glo assay				J Med Chem 59: 253-63 (2016) BindingDB Entry DOI: 10.7270/Q23J3FSW
					More data for this Ligand-Target Pair
Amine oxidase (flavin-containing) A (Homo sapiens (Human))	BDBM50142080 (CHEMBL3758211) Show SMILES N#Cc1ccc(cc1)-c1cc(OCC2CCNCC2)cnc1-c1ccccc1 Show InChI InChI=1S/C24H23N3O/c25-15-18-6-8-20(9-7-18)23-14-22(28-17-19-10-12-26-13-11-19)16-27-24(23)21-4-2-1-3-5-21/h1-9,14,16,19,26H,10-13,17H2	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Baylor College of Medicine Curated by ChEMBL					Assay Description Inhibition of recombinant human MAO-A after 60 mins MAO-glo assay				J Med Chem 59: 253-63 (2016) BindingDB Entry DOI: 10.7270/Q23J3FSW
					More data for this Ligand-Target Pair