BDBM50256407 CHEMBL4088197

SMILES: COc1cc(\C=C\C(=O)OCC2CCN(Cc3ccccc3)CC2)ccc1O

InChI Key: InChIKey=QJDRBHVMOOPIGE-CSKARUKUSA-N

Data: 1 KI  2 IC50

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 3 hits for monomerid = 50256407   

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
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50256407 (CHEMBL4088197) Show SMILES COc1cc(\C=C\C(=O)OCC2CCN(Cc3ccccc3)CC2)ccc1O Show InChI InChI=1S/C23H27NO4/c1-27-22-15-18(7-9-21(22)25)8-10-23(26)28-17-20-11-13-24(14-12-20)16-19-5-3-2-4-6-19/h2-10,15,20,25H,11-14,16-17H2,1H3/b10-8+	GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	1.04E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
PeQuiM- Laboratory of Research in Medicinal Chemistry, Institute of Chemistry, Federal University of Alfenas, 37130-000, Alfenas, MG, Brazil. Curated by ChEMBL					Assay Description Non-competitive inhibition of Electrophorus electricus AChE using acetylthiocholine iodide as substrate pretreated for 10 mins followed by substrate ...				Eur J Med Chem 130: 440-457 (2017) Article DOI: 10.1016/j.ejmech.2017.02.043 BindingDB Entry DOI: 10.7270/Q2VX0JXD
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50256407 (CHEMBL4088197) Show SMILES COc1cc(\C=C\C(=O)OCC2CCN(Cc3ccccc3)CC2)ccc1O Show InChI InChI=1S/C23H27NO4/c1-27-22-15-18(7-9-21(22)25)8-10-23(26)28-17-20-11-13-24(14-12-20)16-19-5-3-2-4-6-19/h2-10,15,20,25H,11-14,16-17H2,1H3/b10-8+	GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	460	n/a	n/a	n/a	n/a	n/a	n/a
PeQuiM- Laboratory of Research in Medicinal Chemistry, Institute of Chemistry, Federal University of Alfenas, 37130-000, Alfenas, MG, Brazil. Curated by ChEMBL					Assay Description Inhibition of Electrophorus electricus AChE using acetylthiocholine iodide as substrate pretreated for 10 mins followed by substrate addition measure...				Eur J Med Chem 130: 440-457 (2017) Article DOI: 10.1016/j.ejmech.2017.02.043 BindingDB Entry DOI: 10.7270/Q2VX0JXD
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50256407 (CHEMBL4088197) Show SMILES COc1cc(\C=C\C(=O)OCC2CCN(Cc3ccccc3)CC2)ccc1O Show InChI InChI=1S/C23H27NO4/c1-27-22-15-18(7-9-21(22)25)8-10-23(26)28-17-20-11-13-24(14-12-20)16-19-5-3-2-4-6-19/h2-10,15,20,25H,11-14,16-17H2,1H3/b10-8+	PDB GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
PeQuiM- Laboratory of Research in Medicinal Chemistry, Institute of Chemistry, Federal University of Alfenas, 37130-000, Alfenas, MG, Brazil. Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate pretreated for 10 mins followed by substrate addition measured at 12 se...				Eur J Med Chem 130: 440-457 (2017) Article DOI: 10.1016/j.ejmech.2017.02.043 BindingDB Entry DOI: 10.7270/Q2VX0JXD
					More data for this Ligand-Target Pair