null

SMILES: [Br-].OC(C(=O)OC1C[N+]2(CCCOc3ccccc3)CCC1CC2)(c1ccccc1)c1ccccc1

InChI Key: InChIKey=SMCLERNDEYAHHL-UHFFFAOYSA-M

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50522814   

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))	BDBM50522814 (CHEMBL4461243) Show SMILES [Br-].OC(C(=O)OC1C[N+]2(CCCOc3ccccc3)CCC1CC2)(c1ccccc1)c1ccccc1 |(13.28,-19.41,;3.37,-21.2,;4.71,-21.98,;6.04,-22.74,;6.05,-24.28,;7.38,-21.97,;8.71,-22.74,;10.04,-21.96,;11.36,-22.74,;12.7,-21.97,;14.03,-22.74,;15.37,-21.97,;16.7,-22.75,;18.03,-21.98,;19.36,-22.76,;20.69,-21.99,;20.7,-20.45,;19.36,-19.68,;18.03,-20.45,;11.37,-24.28,;10.04,-25.04,;8.71,-24.28,;10.2,-24.07,;9.85,-23.02,;4.7,-20.44,;6.03,-19.67,;6.03,-18.13,;4.69,-17.36,;3.36,-18.14,;3.37,-19.68,;3.38,-22.75,;2.04,-21.98,;.71,-22.75,;.72,-24.29,;2.06,-25.06,;3.39,-24.28,)| Show InChI InChI=1S/C30H34NO4.BrH/c32-29(30(33,25-11-4-1-5-12-25)26-13-6-2-7-14-26)35-28-23-31(20-17-24(28)18-21-31)19-10-22-34-27-15-8-3-9-16-27;/h1-9,11-16,24,28,33H,10,17-23H2;1H/q+1;/p-1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	0.680	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
					More data for this Ligand-Target Pair
Muscarinic acetylcholine receptor M3 (Homo sapiens (Human))	BDBM50522814 (CHEMBL4461243) Show SMILES [Br-].OC(C(=O)OC1C[N+]2(CCCOc3ccccc3)CCC1CC2)(c1ccccc1)c1ccccc1 |(13.28,-19.41,;3.37,-21.2,;4.71,-21.98,;6.04,-22.74,;6.05,-24.28,;7.38,-21.97,;8.71,-22.74,;10.04,-21.96,;11.36,-22.74,;12.7,-21.97,;14.03,-22.74,;15.37,-21.97,;16.7,-22.75,;18.03,-21.98,;19.36,-22.76,;20.69,-21.99,;20.7,-20.45,;19.36,-19.68,;18.03,-20.45,;11.37,-24.28,;10.04,-25.04,;8.71,-24.28,;10.2,-24.07,;9.85,-23.02,;4.7,-20.44,;6.03,-19.67,;6.03,-18.13,;4.69,-17.36,;3.36,-18.14,;3.37,-19.68,;3.38,-22.75,;2.04,-21.98,;.71,-22.75,;.72,-24.29,;2.06,-25.06,;3.39,-24.28,)| Show InChI InChI=1S/C30H34NO4.BrH/c32-29(30(33,25-11-4-1-5-12-25)26-13-6-2-7-14-26)35-28-23-31(20-17-24(28)18-21-31)19-10-22-34-27-15-8-3-9-16-27;/h1-9,11-16,24,28,33H,10,17-23H2;1H/q+1;/p-1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	0.880	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
					More data for this Ligand-Target Pair