null

SMILES: CCN(CC)CC#CCN1C(=O)CC2(C1=O)c1ccccc1CCc1ccccc21

InChI Key: InChIKey=XGDYJGHYOOFXOA-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50291591   

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)	BDBM50291591 (1'-(4-diethylamino-2-butynyl)spiro[10,11-dihydro-5...) Show SMILES CCN(CC)CC#CCN1C(=O)CC2(C1=O)c1ccccc1CCc1ccccc21 Show InChI InChI=1S/C26H28N2O2/c1-3-27(4-2)17-9-10-18-28-24(29)19-26(25(28)30)22-13-7-5-11-20(22)15-16-21-12-6-8-14-23(21)26/h5-8,11-14H,3-4,15-19H2,1-2H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	460	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)	BDBM50291591 (1'-(4-diethylamino-2-butynyl)spiro[10,11-dihydro-5...) Show SMILES CCN(CC)CC#CCN1C(=O)CC2(C1=O)c1ccccc1CCc1ccccc21 Show InChI InChI=1S/C26H28N2O2/c1-3-27(4-2)17-9-10-18-28-24(29)19-26(25(28)30)22-13-7-5-11-20(22)15-16-21-12-6-8-14-23(21)26/h5-8,11-14H,3-4,15-19H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	2.09E+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]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