null

SMILES: [Br-].OC(C(=O)OC1C[N+]2(CCCc3ccc(Br)cc3)CCC1CC2)(c1ccccc1)c1ccccc1

InChI Key: InChIKey=ZQEYACYDEGWAAF-UHFFFAOYSA-M

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50522813   

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
Muscarinic acetylcholine receptor M2 (Homo sapiens (Human))	BDBM50522813 (CHEMBL4539799) Show SMILES [Br-].OC(C(=O)OC1C[N+]2(CCCc3ccc(Br)cc3)CCC1CC2)(c1ccccc1)c1ccccc1 |(60.03,-19.13,;50.39,-21.97,;51.73,-22.75,;53.06,-23.51,;53.07,-25.05,;54.39,-22.74,;55.73,-23.51,;57.06,-22.73,;58.38,-23.51,;59.72,-22.74,;61.05,-23.51,;62.38,-22.74,;63.72,-23.52,;63.71,-25.05,;65.04,-25.83,;66.38,-25.06,;67.71,-25.83,;66.37,-23.51,;65.04,-22.75,;58.39,-25.05,;57.06,-25.81,;55.73,-25.05,;57.22,-24.84,;56.87,-23.79,;51.72,-21.21,;53.05,-20.44,;53.05,-18.9,;51.71,-18.13,;50.38,-18.91,;50.39,-20.45,;50.39,-23.52,;49.06,-22.75,;47.73,-23.52,;47.73,-25.06,;49.08,-25.83,;50.4,-25.05,)| Show InChI InChI=1S/C30H33BrNO3.BrH/c31-27-15-13-23(14-16-27)8-7-19-32-20-17-24(18-21-32)28(22-32)35-29(33)30(34,25-9-3-1-4-10-25)26-11-5-2-6-12-26;/h1-6,9-16,24,28,34H,7-8,17-22H2;1H/q+1;/p-1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	1.60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Advanced Industrial Science and Technology (AIST) Curated by ChEMBL					Assay Description Displacement of [3H]NMS from human M2R expressed in CHOK1 cell membranes incubated for 2 hrs by microbeta scintillation counting method				Bioorg Med Chem 27: 3339-3346 (2019) Article DOI: 10.1016/j.bmc.2019.06.016 BindingDB Entry DOI: 10.7270/Q2DR2ZXC
					More data for this Ligand-Target Pair
Muscarinic acetylcholine receptor M3 (Homo sapiens (Human))	BDBM50522813 (CHEMBL4539799) Show SMILES [Br-].OC(C(=O)OC1C[N+]2(CCCc3ccc(Br)cc3)CCC1CC2)(c1ccccc1)c1ccccc1 |(60.03,-19.13,;50.39,-21.97,;51.73,-22.75,;53.06,-23.51,;53.07,-25.05,;54.39,-22.74,;55.73,-23.51,;57.06,-22.73,;58.38,-23.51,;59.72,-22.74,;61.05,-23.51,;62.38,-22.74,;63.72,-23.52,;63.71,-25.05,;65.04,-25.83,;66.38,-25.06,;67.71,-25.83,;66.37,-23.51,;65.04,-22.75,;58.39,-25.05,;57.06,-25.81,;55.73,-25.05,;57.22,-24.84,;56.87,-23.79,;51.72,-21.21,;53.05,-20.44,;53.05,-18.9,;51.71,-18.13,;50.38,-18.91,;50.39,-20.45,;50.39,-23.52,;49.06,-22.75,;47.73,-23.52,;47.73,-25.06,;49.08,-25.83,;50.4,-25.05,)| Show InChI InChI=1S/C30H33BrNO3.BrH/c31-27-15-13-23(14-16-27)8-7-19-32-20-17-24(18-21-32)28(22-32)35-29(33)30(34,25-9-3-1-4-10-25)26-11-5-2-6-12-26;/h1-6,9-16,24,28,34H,7-8,17-22H2;1H/q+1;/p-1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	2.60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Advanced Industrial Science and Technology (AIST) Curated by ChEMBL					Assay Description Displacement of [3H]NMS from human M3R expressed in CHOK1 cell membranes incubated for 2 hrs by microbeta scintillation counting method				Bioorg Med Chem 27: 3339-3346 (2019) Article DOI: 10.1016/j.bmc.2019.06.016 BindingDB Entry DOI: 10.7270/Q2DR2ZXC
					More data for this Ligand-Target Pair