null

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

InChI Key: InChIKey=GBCWXWXBNFRMHD-UHFFFAOYSA-M

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50522821   

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))	BDBM50522821 (CHEMBL4450188) Show SMILES [Br-].OC(C(=O)OC1C[N+]2(CCCc3ccc(F)cc3)CCC1CC2)(c1ccccc1)c1ccccc1 |(13.36,-19.18,;4.01,-20.28,;5.35,-21.05,;6.68,-21.82,;6.69,-23.36,;8.01,-21.04,;9.35,-21.81,;10.68,-21.03,;12,-21.81,;13.34,-21.04,;14.67,-21.82,;16,-21.05,;17.34,-21.82,;17.33,-23.36,;18.66,-24.13,;20,-23.36,;21.33,-24.14,;20,-21.82,;18.66,-21.05,;12.01,-23.35,;10.68,-24.11,;9.35,-23.35,;10.84,-23.15,;10.49,-22.1,;5.34,-19.51,;6.67,-18.74,;6.67,-17.2,;5.33,-16.43,;4,-17.22,;4.01,-18.75,;4.01,-21.83,;2.68,-21.05,;1.35,-21.83,;1.35,-23.37,;2.7,-24.13,;4.02,-23.36,)| Show InChI InChI=1S/C30H33FNO3.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	0.490	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))	BDBM50522821 (CHEMBL4450188) Show SMILES [Br-].OC(C(=O)OC1C[N+]2(CCCc3ccc(F)cc3)CCC1CC2)(c1ccccc1)c1ccccc1 |(13.36,-19.18,;4.01,-20.28,;5.35,-21.05,;6.68,-21.82,;6.69,-23.36,;8.01,-21.04,;9.35,-21.81,;10.68,-21.03,;12,-21.81,;13.34,-21.04,;14.67,-21.82,;16,-21.05,;17.34,-21.82,;17.33,-23.36,;18.66,-24.13,;20,-23.36,;21.33,-24.14,;20,-21.82,;18.66,-21.05,;12.01,-23.35,;10.68,-24.11,;9.35,-23.35,;10.84,-23.15,;10.49,-22.1,;5.34,-19.51,;6.67,-18.74,;6.67,-17.2,;5.33,-16.43,;4,-17.22,;4.01,-18.75,;4.01,-21.83,;2.68,-21.05,;1.35,-21.83,;1.35,-23.37,;2.7,-24.13,;4.02,-23.36,)| Show InChI InChI=1S/C30H33FNO3.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	1.70	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