null

SMILES: CCCCCCOc1nccnc1[C@@H]1CN2CC1CCC2

InChI Key: InChIKey=UNWLHKNSDBYWHQ-YSSOQSIOSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50033156   

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)	BDBM50033156 ((S)-6-(3-Hexyloxy-pyrazin-2-yl)-1-aza-bicyclo[3.2....) Show SMILES CCCCCCOc1nccnc1[C@@H]1CN2CC1CCC2 |THB:12:13:16:20.18.19| Show InChI InChI=1S/C17H27N3O/c1-2-3-4-5-11-21-17-16(18-8-9-19-17)15-13-20-10-6-7-14(15)12-20/h8-9,14-15H,2-7,10-13H2,1H3/t14?,15-/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	180	n/a	n/a	n/a	n/a	n/a	n/a
Lilly Research Laboratories Curated by ChEMBL					Assay Description Binding activity against muscarinic acetylcholine receptor M1 in rat brain, using [3H]OXO-M as the radioligand.				J Med Chem 38: 3469-81 (1995) BindingDB Entry DOI: 10.7270/Q2TB17JZ
					More data for this Ligand-Target Pair
Muscarinic acetylcholine receptor M1 (RAT)	BDBM50033156 ((S)-6-(3-Hexyloxy-pyrazin-2-yl)-1-aza-bicyclo[3.2....) Show SMILES CCCCCCOc1nccnc1[C@@H]1CN2CC1CCC2 |THB:12:13:16:20.18.19| Show InChI InChI=1S/C17H27N3O/c1-2-3-4-5-11-21-17-16(18-8-9-19-17)15-13-20-10-6-7-14(15)12-20/h8-9,14-15H,2-7,10-13H2,1H3/t14?,15-/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	120	n/a	n/a	n/a	n/a	n/a	n/a
Lilly Research Laboratories Curated by ChEMBL					Assay Description Binding activity against muscarinic acetylcholine receptor M1 in rat brain, using [3H]-Pz as the radioligand.				J Med Chem 38: 3469-81 (1995) BindingDB Entry DOI: 10.7270/Q2TB17JZ
					More data for this Ligand-Target Pair