Compile Data Set for Download or QSAR

Found 5 hits Enz. Inhib. hit(s) with Target = 'Muscarinic acetylcholine receptor M1' and Ligand = 'BDBM50003350'   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Muscarinic acetylcholine receptor M1 (RAT)	BDBM50003350 (5-(4-Heptyl-[1,2,5]thiadiazol-3-yl)-1-methyl-1,2,3...) Show SMILES CCCCCCCc1nsnc1C1=CCCN(C)C1 |t:13| Show InChI InChI=1S/C15H25N3S/c1-3-4-5-6-7-10-14-15(17-19-16-14)13-9-8-11-18(2)12-13/h9H,3-8,10-12H2,1-2H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	73	n/a	n/a	n/a	n/a	n/a	n/a
Novo Nordisk CNS Division Curated by ChEMBL					Assay Description In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-oxotremorine-M (Oxo-M) as radioligand				J Med Chem 35: 2274-83 (1992) BindingDB Entry DOI: 10.7270/Q22J69TH
					More data for this Ligand-Target Pair
Muscarinic acetylcholine receptor M1 (RAT)	BDBM50003350 (5-(4-Heptyl-[1,2,5]thiadiazol-3-yl)-1-methyl-1,2,3...) Show SMILES CCCCCCCc1nsnc1C1=CCCN(C)C1 |t:13| Show InChI InChI=1S/C15H25N3S/c1-3-4-5-6-7-10-14-15(17-19-16-14)13-9-8-11-18(2)12-13/h9H,3-8,10-12H2,1-2H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	73	n/a	n/a	n/a	n/a	n/a	n/a
Lilly Research Laboratories Curated by ChEMBL					Assay Description Displacement of [3H]-pirenzepine (Pz) 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)	BDBM50003350 (5-(4-Heptyl-[1,2,5]thiadiazol-3-yl)-1-methyl-1,2,3...) Show SMILES CCCCCCCc1nsnc1C1=CCCN(C)C1 |t:13| Show InChI InChI=1S/C15H25N3S/c1-3-4-5-6-7-10-14-15(17-19-16-14)13-9-8-11-18(2)12-13/h9H,3-8,10-12H2,1-2H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	187	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]-pirenzepine (Pz) 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)	BDBM50003350 (5-(4-Heptyl-[1,2,5]thiadiazol-3-yl)-1-methyl-1,2,3...) Show SMILES CCCCCCCc1nsnc1C1=CCCN(C)C1 |t:13| Show InChI InChI=1S/C15H25N3S/c1-3-4-5-6-7-10-14-15(17-19-16-14)13-9-8-11-18(2)12-13/h9H,3-8,10-12H2,1-2H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	187	n/a	n/a	n/a	n/a	n/a	n/a
Novo Nordisk CNS Division Curated by ChEMBL					Assay Description In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-oxotremorine-M (Oxo-M) as radioligand				J Med Chem 35: 2274-83 (1992) BindingDB Entry DOI: 10.7270/Q22J69TH
					More data for this Ligand-Target Pair
Muscarinic acetylcholine receptor M1 (Homo sapiens (Human))	BDBM50003350 (5-(4-Heptyl-[1,2,5]thiadiazol-3-yl)-1-methyl-1,2,3...) Show SMILES CCCCCCCc1nsnc1C1=CCCN(C)C1 |t:13| Show InChI InChI=1S/C15H25N3S/c1-3-4-5-6-7-10-14-15(17-19-16-14)13-9-8-11-18(2)12-13/h9H,3-8,10-12H2,1-2H3	UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	224	n/a	n/a	n/a	n/a	n/a	n/a
Lilly Research Laboratories Curated by ChEMBL					Assay Description Efficacy at muscarinic acetylcholine receptor M1 measured by the ability to inhibit the electrically stimulated twitch of the rabbit vas deferens				J Med Chem 35: 4011-9 (1992) BindingDB Entry DOI: 10.7270/Q2KW5F1K
					More data for this Ligand-Target Pair