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SMILES: C[C@H](Cc1ccc(OCCCCCCCCNc2c3CCCCc3nc3ccccc23)cc1)N(C)CC#C

InChI Key: InChIKey=UHBQVRDIKUXATE-HHHXNRCGSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50430732   

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
Amine oxidase [flavin-containing] B (Homo sapiens (Human))	BDBM50430732 (CHEMBL2333937) Show SMILES C[C@H](Cc1ccc(OCCCCCCCCNc2c3CCCCc3nc3ccccc23)cc1)N(C)CC#C |r| Show InChI InChI=1S/C34H45N3O/c1-4-24-37(3)27(2)26-28-19-21-29(22-20-28)38-25-14-8-6-5-7-13-23-35-34-30-15-9-11-17-32(30)36-33-18-12-10-16-31(33)34/h1,9,11,15,17,19-22,27H,5-8,10,12-14,16,18,23-26H2,2-3H3,(H,35,36)/t27-/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	167	n/a	n/a	n/a	n/a	n/a	n/a
Sun Yat-sen University Curated by ChEMBL					Assay Description Inhibition of recombinant human MAO-B using p-benzylamine substrate preincubated for 15 mins before substrate addition measured after 20 mins by fluo...				Eur J Med Chem 62: 745-53 (2013) Article DOI: 10.1016/j.ejmech.2013.01.039 BindingDB Entry DOI: 10.7270/Q2C82BN6
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50430732 (CHEMBL2333937) Show SMILES C[C@H](Cc1ccc(OCCCCCCCCNc2c3CCCCc3nc3ccccc23)cc1)N(C)CC#C |r| Show InChI InChI=1S/C34H45N3O/c1-4-24-37(3)27(2)26-28-19-21-29(22-20-28)38-25-14-8-6-5-7-13-23-35-34-30-15-9-11-17-32(30)36-33-18-12-10-16-31(33)34/h1,9,11,15,17,19-22,27H,5-8,10,12-14,16,18,23-26H2,2-3H3,(H,35,36)/t27-/m1/s1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	147	n/a	n/a	n/a	n/a	n/a	n/a
Sun Yat-sen University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine chloride as substrate after 15 mins by Ellman's method				Eur J Med Chem 62: 745-53 (2013) Article DOI: 10.1016/j.ejmech.2013.01.039 BindingDB Entry DOI: 10.7270/Q2C82BN6
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50430732 (CHEMBL2333937) Show SMILES C[C@H](Cc1ccc(OCCCCCCCCNc2c3CCCCc3nc3ccccc23)cc1)N(C)CC#C |r| Show InChI InChI=1S/C34H45N3O/c1-4-24-37(3)27(2)26-28-19-21-29(22-20-28)38-25-14-8-6-5-7-13-23-35-34-30-15-9-11-17-32(30)36-33-18-12-10-16-31(33)34/h1,9,11,15,17,19-22,27H,5-8,10,12-14,16,18,23-26H2,2-3H3,(H,35,36)/t27-/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	36	n/a	n/a	n/a	n/a	n/a	n/a
Sun Yat-sen University Curated by ChEMBL					Assay Description Inhibition of horse serum BChE using butylthiocholine chloride as substrate after 15 mins by Ellman's method				Eur J Med Chem 62: 745-53 (2013) Article DOI: 10.1016/j.ejmech.2013.01.039 BindingDB Entry DOI: 10.7270/Q2C82BN6
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] A (Homo sapiens (Human))	BDBM50430732 (CHEMBL2333937) Show SMILES C[C@H](Cc1ccc(OCCCCCCCCNc2c3CCCCc3nc3ccccc23)cc1)N(C)CC#C |r| Show InChI InChI=1S/C34H45N3O/c1-4-24-37(3)27(2)26-28-19-21-29(22-20-28)38-25-14-8-6-5-7-13-23-35-34-30-15-9-11-17-32(30)36-33-18-12-10-16-31(33)34/h1,9,11,15,17,19-22,27H,5-8,10,12-14,16,18,23-26H2,2-3H3,(H,35,36)/t27-/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	591	n/a	n/a	n/a	n/a	n/a	n/a
Sun Yat-sen University Curated by ChEMBL					Assay Description Inhibition of recombinant human MAO-A using p-tyramine substrate preincubated for 15 mins before substrate addition measured after 20 mins by fluores...				Eur J Med Chem 62: 745-53 (2013) Article DOI: 10.1016/j.ejmech.2013.01.039 BindingDB Entry DOI: 10.7270/Q2C82BN6
					More data for this Ligand-Target Pair