null

SMILES: Cc1nc(cs1)C(=O)N1CCOC2(CCN(Cc3ccccc3Cl)CC2)C1

InChI Key: InChIKey=LYQGZYIUMYUMCO-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50417457   

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 M2 (Homo sapiens (Human))	BDBM50417457 (CHEMBL1289654) Show SMILES Cc1nc(cs1)C(=O)N1CCOC2(CCN(Cc3ccccc3Cl)CC2)C1 Show InChI InChI=1S/C20H24ClN3O2S/c1-15-22-18(13-27-15)19(25)24-10-11-26-20(14-24)6-8-23(9-7-20)12-16-4-2-3-5-17(16)21/h2-5,13H,6-12,14H2,1H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.16	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Displacement of [3H]NMS from human muscarinic M2 receptor expressed in CHO-K1 cells after 16 hrs by scintillation proximity assay				Bioorg Med Chem Lett 20: 7458-61 (2010) Article DOI: 10.1016/j.bmcl.2010.10.016 BindingDB Entry DOI: 10.7270/Q2GM88K4
					More data for this Ligand-Target Pair
Muscarinic acetylcholine receptor M3 (Homo sapiens (Human))	BDBM50417457 (CHEMBL1289654) Show SMILES Cc1nc(cs1)C(=O)N1CCOC2(CCN(Cc3ccccc3Cl)CC2)C1 Show InChI InChI=1S/C20H24ClN3O2S/c1-15-22-18(13-27-15)19(25)24-10-11-26-20(14-24)6-8-23(9-7-20)12-16-4-2-3-5-17(16)21/h2-5,13H,6-12,14H2,1H3	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.94	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Displacement of [3H]NMS from human muscarinic M3 receptor expressed in CHO-K1 cells after 16 hrs by scintillation proximity assay				Bioorg Med Chem Lett 20: 7458-61 (2010) Article DOI: 10.1016/j.bmcl.2010.10.016 BindingDB Entry DOI: 10.7270/Q2GM88K4
					More data for this Ligand-Target Pair