null

SMILES: [Br-].OC(C(=O)OC1C[N+]2(CCCCCc3ccccc3)CCC1CC2)(c1ccccc1)c1ccccc1

InChI Key: InChIKey=AFFIUYZBOODVTQ-UHFFFAOYSA-M

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50522812   

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))	BDBM50522812 (CHEMBL4436947) Show SMILES [Br-].OC(C(=O)OC1C[N+]2(CCCCCc3ccccc3)CCC1CC2)(c1ccccc1)c1ccccc1 |(37.82,-49.13,;27.42,-51.16,;28.76,-51.93,;30.1,-52.7,;30.11,-54.24,;31.43,-51.92,;32.77,-52.69,;34.1,-51.91,;35.42,-52.69,;36.76,-51.92,;38.09,-52.69,;39.42,-51.93,;40.76,-52.7,;42.09,-51.93,;43.42,-52.7,;43.42,-54.25,;44.75,-55.02,;46.08,-54.25,;46.08,-52.7,;44.75,-51.94,;35.43,-54.23,;34.1,-54.99,;32.77,-54.23,;34.26,-54.03,;33.91,-52.98,;28.76,-50.39,;30.09,-49.62,;30.09,-48.08,;28.75,-47.31,;27.42,-48.09,;27.43,-49.63,;27.43,-52.7,;26.1,-51.93,;24.77,-52.7,;24.77,-54.25,;26.12,-55.01,;27.44,-54.23,)| Show InChI InChI=1S/C32H38NO3.BrH/c34-31(32(35,28-16-8-2-9-17-28)29-18-10-3-11-19-29)36-30-25-33(23-20-27(30)21-24-33)22-12-4-7-15-26-13-5-1-6-14-26;/h1-3,5-6,8-11,13-14,16-19,27,30,35H,4,7,12,15,20-25H2;1H/q+1;/p-1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	7.10	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))	BDBM50522812 (CHEMBL4436947) Show SMILES [Br-].OC(C(=O)OC1C[N+]2(CCCCCc3ccccc3)CCC1CC2)(c1ccccc1)c1ccccc1 |(37.82,-49.13,;27.42,-51.16,;28.76,-51.93,;30.1,-52.7,;30.11,-54.24,;31.43,-51.92,;32.77,-52.69,;34.1,-51.91,;35.42,-52.69,;36.76,-51.92,;38.09,-52.69,;39.42,-51.93,;40.76,-52.7,;42.09,-51.93,;43.42,-52.7,;43.42,-54.25,;44.75,-55.02,;46.08,-54.25,;46.08,-52.7,;44.75,-51.94,;35.43,-54.23,;34.1,-54.99,;32.77,-54.23,;34.26,-54.03,;33.91,-52.98,;28.76,-50.39,;30.09,-49.62,;30.09,-48.08,;28.75,-47.31,;27.42,-48.09,;27.43,-49.63,;27.43,-52.7,;26.1,-51.93,;24.77,-52.7,;24.77,-54.25,;26.12,-55.01,;27.44,-54.23,)| Show InChI InChI=1S/C32H38NO3.BrH/c34-31(32(35,28-16-8-2-9-17-28)29-18-10-3-11-19-29)36-30-25-33(23-20-27(30)21-24-33)22-12-4-7-15-26-13-5-1-6-14-26;/h1-3,5-6,8-11,13-14,16-19,27,30,35H,4,7,12,15,20-25H2;1H/q+1;/p-1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	17	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