null

SMILES: CCCSc1nsnc1C1CN2CCC1C2

InChI Key: InChIKey=YTGOXLHANZIGKG-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50062595   

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)	BDBM50062595 (3-(4-Propylsulfanyl-[1,2,5]thiadiazol-3-yl)-1-aza-...) Show SMILES CCCSc1nsnc1C1CN2CCC1C2 |THB:8:9:15:13.12| Show InChI InChI=1S/C11H17N3S2/c1-2-5-15-11-10(12-16-13-11)9-7-14-4-3-8(9)6-14/h8-9H,2-7H2,1H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	5.80	n/a	n/a	n/a	n/a	n/a	n/a
Lilly Research Laboratories Curated by ChEMBL					Assay Description Binding affinity for muscarinic acetylcholine receptor M1 using [3H]-oxotremorine-M (Oxo-M) radioligand in rat hippocampus membranes				J Med Chem 41: 379-92 (1998) Article DOI: 10.1021/jm970125n BindingDB Entry DOI: 10.7270/Q2SX6CBC
					More data for this Ligand-Target Pair
Muscarinic acetylcholine receptor M1 (RAT)	BDBM50062595 (3-(4-Propylsulfanyl-[1,2,5]thiadiazol-3-yl)-1-aza-...) Show SMILES CCCSc1nsnc1C1CN2CCC1C2 |THB:8:9:15:13.12| Show InChI InChI=1S/C11H17N3S2/c1-2-5-15-11-10(12-16-13-11)9-7-14-4-3-8(9)6-14/h8-9H,2-7H2,1H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	5.80	n/a	n/a	n/a	n/a	n/a	n/a
Lilly Research Laboratories Curated by ChEMBL					Assay Description Binding affinity for muscarinic acetylcholine receptor M1 using [3H]-oxotremorine-M (Oxo-M) radioligand in rat hippocampus membranes				J Med Chem 41: 379-92 (1998) Article DOI: 10.1021/jm970125n BindingDB Entry DOI: 10.7270/Q2SX6CBC
					More data for this Ligand-Target Pair