null

SMILES: CCN(CC)CC#CCN1C(=O)CC(C1=O)c1ccccc1

InChI Key: InChIKey=JRMWVTUADFJHPB-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50291594   

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 M1 (RAT)	BDBM50291594 (1-(4-Diethylamino-but-2-ynyl)-3-phenyl-pyrrolidine...) Show SMILES CCN(CC)CC#CCN1C(=O)CC(C1=O)c1ccccc1 Show InChI InChI=1S/C18H22N2O2/c1-3-19(4-2)12-8-9-13-20-17(21)14-16(18(20)22)15-10-6-5-7-11-15/h5-7,10-11,16H,3-4,12-14H2,1-2H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	2.30E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Displacement of [3H]pirenzepine from muscarinic M1 receptor of rat cortex homogenates.				Bioorg Med Chem Lett 7: 979-984 (1997) Article DOI: 10.1016/S0960-894X(97)00143-1 BindingDB Entry DOI: 10.7270/Q2N29XFM
					More data for this Ligand-Target Pair
Muscarinic acetylcholine receptor M2 (RAT)	BDBM50291594 (1-(4-Diethylamino-but-2-ynyl)-3-phenyl-pyrrolidine...) Show SMILES CCN(CC)CC#CCN1C(=O)CC(C1=O)c1ccccc1 Show InChI InChI=1S/C18H22N2O2/c1-3-19(4-2)12-8-9-13-20-17(21)14-16(18(20)22)15-10-6-5-7-11-15/h5-7,10-11,16H,3-4,12-14H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Displacement of [3H]QNB (quinuclidinyl benzylate) from muscarinic M2 receptor of rat heart homogenates.				Bioorg Med Chem Lett 7: 979-984 (1997) Article DOI: 10.1016/S0960-894X(97)00143-1 BindingDB Entry DOI: 10.7270/Q2N29XFM
					More data for this Ligand-Target Pair