null

SMILES: O=C1NC(CN1C1CCN(Cc2ccccc2)CC1)(c1cccs1)c1cccs1

InChI Key: InChIKey=PAWBGCCWTWGZPD-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50208024   

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 M3 (Homo sapiens (Human))	BDBM50208024 (3-(1-benzyl-piperidin-4-yl)-5,5-di-(2-thienyl)-imi...) Show SMILES O=C1NC(CN1C1CCN(Cc2ccccc2)CC1)(c1cccs1)c1cccs1 Show InChI InChI=1S/C23H25N3OS2/c27-22-24-23(20-8-4-14-28-20,21-9-5-15-29-21)17-26(22)19-10-12-25(13-11-19)16-18-6-2-1-3-7-18/h1-9,14-15,19H,10-13,16-17H2,(H,24,27)	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.70	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Via Zambeletti 25 Curated by ChEMBL					Assay Description Displacement of [3H]N-methyl-scopalamine from human muscarinic M3 receptor expressed in CHO K1 cells				J Med Chem 50: 1571-83 (2007) Article DOI: 10.1021/jm061159a BindingDB Entry DOI: 10.7270/Q2QV3M61
					More data for this Ligand-Target Pair
Muscarinic acetylcholine receptor M2 (Homo sapiens (Human))	BDBM50208024 (3-(1-benzyl-piperidin-4-yl)-5,5-di-(2-thienyl)-imi...) Show SMILES O=C1NC(CN1C1CCN(Cc2ccccc2)CC1)(c1cccs1)c1cccs1 Show InChI InChI=1S/C23H25N3OS2/c27-22-24-23(20-8-4-14-28-20,21-9-5-15-29-21)17-26(22)19-10-12-25(13-11-19)16-18-6-2-1-3-7-18/h1-9,14-15,19H,10-13,16-17H2,(H,24,27)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	96.8	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Via Zambeletti 25 Curated by ChEMBL					Assay Description Displacement of [3H]N-methyl-scopalamine from human muscarinic M2 receptor expressed in CHO K1 cells				J Med Chem 50: 1571-83 (2007) Article DOI: 10.1021/jm061159a BindingDB Entry DOI: 10.7270/Q2QV3M61
					More data for this Ligand-Target Pair