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SMILES: CCCCCCOc1nscc1C1=CCCN(C)C1

InChI Key: InChIKey=FBKNMNSUKXGQCW-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50280530   

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/M2/M3/M4/M5 (RAT)	BDBM50280530 (5-(3-Hexyloxy-isothiazol-4-yl)-1-methyl-1,2,3,6-te...) Show SMILES CCCCCCOc1nscc1C1=CCCN(C)C1 |t:13| Show InChI InChI=1S/C15H24N2OS/c1-3-4-5-6-10-18-15-14(12-19-16-15)13-8-7-9-17(2)11-13/h8,12H,3-7,9-11H2,1-2H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	>900	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Displacement of [3H]-OXO-M (oxotremorine-M) from the central muscarinic receptor sites of the rat brain membranes				Bioorg Med Chem Lett 2: 809-814 (1992) Article DOI: 10.1016/S0960-894X(00)80536-3 BindingDB Entry DOI: 10.7270/Q2T72HBX
					More data for this Ligand-Target Pair
Muscarinic acetylcholine receptor M1 (RAT)	BDBM50280530 (5-(3-Hexyloxy-isothiazol-4-yl)-1-methyl-1,2,3,6-te...) Show SMILES CCCCCCOc1nscc1C1=CCCN(C)C1 |t:13| Show InChI InChI=1S/C15H24N2OS/c1-3-4-5-6-10-18-15-14(12-19-16-15)13-8-7-9-17(2)11-13/h8,12H,3-7,9-11H2,1-2H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	715	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Displacement of [3H]-Pz (pirenzepine) from the muscarinic receptor M1 of the rat hippocampus				Bioorg Med Chem Lett 2: 809-814 (1992) Article DOI: 10.1016/S0960-894X(00)80536-3 BindingDB Entry DOI: 10.7270/Q2T72HBX
					More data for this Ligand-Target Pair