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SMILES: CCCCCCOc1nccnc1C1=CCCN(C)C1

InChI Key: InChIKey=LHGYIMYBLIFNAI-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50003364   

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)	BDBM50003364 (2-Hexyloxy-3-(1-methyl-1,2,5,6-tetrahydro-pyridin-...) Show SMILES CCCCCCOc1nccnc1C1=CCCN(C)C1 |t:14| Show InChI InChI=1S/C16H25N3O/c1-3-4-5-6-12-20-16-15(17-9-10-18-16)14-8-7-11-19(2)13-14/h8-10H,3-7,11-13H2,1-2H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	20	n/a	n/a	n/a	n/a	n/a	n/a
Lilly Research Laboratories Curated by ChEMBL					Assay Description In vitro binding affinity against rat hippocampus M1 receptor using [3H]-oxotremorine-M (Oxo-M) as radioligand				J Med Chem 35: 4011-9 (1992) BindingDB Entry DOI: 10.7270/Q2KW5F1K
					More data for this Ligand-Target Pair
Muscarinic acetylcholine receptor M1 (RAT)	BDBM50003364 (2-Hexyloxy-3-(1-methyl-1,2,5,6-tetrahydro-pyridin-...) Show SMILES CCCCCCOc1nccnc1C1=CCCN(C)C1 |t:14| Show InChI InChI=1S/C16H25N3O/c1-3-4-5-6-12-20-16-15(17-9-10-18-16)14-8-7-11-19(2)13-14/h8-10H,3-7,11-13H2,1-2H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	17	n/a	n/a	n/a	n/a	n/a	n/a
Lilly Research Laboratories Curated by ChEMBL					Assay Description Displacement of [3H]-oxotremorine-M (Oxo-M) from rat hippocampus muscarinic acetylcholine receptor M1				J Med Chem 35: 4011-9 (1992) BindingDB Entry DOI: 10.7270/Q2KW5F1K
					More data for this Ligand-Target Pair
Muscarinic acetylcholine receptor M1 (RAT)	BDBM50003364 (2-Hexyloxy-3-(1-methyl-1,2,5,6-tetrahydro-pyridin-...) Show SMILES CCCCCCOc1nccnc1C1=CCCN(C)C1 |t:14| Show InChI InChI=1S/C16H25N3O/c1-3-4-5-6-12-20-16-15(17-9-10-18-16)14-8-7-11-19(2)13-14/h8-10H,3-7,11-13H2,1-2H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	17	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
Muscarinic acetylcholine receptor M1 (RAT)	BDBM50003364 (2-Hexyloxy-3-(1-methyl-1,2,5,6-tetrahydro-pyridin-...) Show SMILES CCCCCCOc1nccnc1C1=CCCN(C)C1 |t:14| Show InChI InChI=1S/C16H25N3O/c1-3-4-5-6-12-20-16-15(17-9-10-18-16)14-8-7-11-19(2)13-14/h8-10H,3-7,11-13H2,1-2H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	20	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