null

SMILES: C(CC[n+]1ccc2ccccc2c1)CC[n+]1ccc2ccccc2c1

InChI Key: InChIKey=HRBRHVOBBAKORO-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50336120   

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
Cholinesterase (Homo sapiens (Human))	BDBM50336120 (1,5-Bis(isoquinolinium)-pent-1,5-diyl dibromide | ...) Show SMILES C(CC[n+]1ccc2ccccc2c1)CC[n+]1ccc2ccccc2c1 Show InChI InChI=1S/C23H24N2/c1(6-14-24-16-12-20-8-2-4-10-22(20)18-24)7-15-25-17-13-21-9-3-5-11-23(21)19-25/h2-5,8-13,16-19H,1,6-7,14-15H2/q+2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	700	n/a	n/a	n/a	n/a	n/a	n/a
University of Defence Curated by ChEMBL					Assay Description Inhibition of human plasmatic BChE by Lineweaver-Burk plot analysis				Eur J Med Chem 46: 811-8 (2011) Article DOI: 10.1016/j.ejmech.2010.12.011 BindingDB Entry DOI: 10.7270/Q2PR7W8D
					More data for this Ligand-Target Pair
Acetylcholinesterase (Homo sapiens (Human))	BDBM50336120 (1,5-Bis(isoquinolinium)-pent-1,5-diyl dibromide | ...) Show SMILES C(CC[n+]1ccc2ccccc2c1)CC[n+]1ccc2ccccc2c1 Show InChI InChI=1S/C23H24N2/c1(6-14-24-16-12-20-8-2-4-10-22(20)18-24)7-15-25-17-13-21-9-3-5-11-23(21)19-25/h2-5,8-13,16-19H,1,6-7,14-15H2/q+2	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Defence Curated by ChEMBL					Assay Description Inhibition of human recombinant AChE by Lineweaver-Burk plot analysis				Eur J Med Chem 46: 811-8 (2011) Article DOI: 10.1016/j.ejmech.2010.12.011 BindingDB Entry DOI: 10.7270/Q2PR7W8D
					More data for this Ligand-Target Pair