BDBM50426256 CHEMBL2312358

SMILES: COc1ccc(CCOC(=O)C2=C(CCN(C)C2)c2ccccc2)cc1

InChI Key: InChIKey=VYVYCDJDMPVQTH-UHFFFAOYSA-N

Data: 2 KI

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50426256   

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 (Homo sapiens (Human))	BDBM50426256 (CHEMBL2312358) Show SMILES COc1ccc(CCOC(=O)C2=C(CCN(C)C2)c2ccccc2)cc1 |t:11| Show InChI InChI=1S/C22H25NO3/c1-23-14-12-20(18-6-4-3-5-7-18)21(16-23)22(24)26-15-13-17-8-10-19(25-2)11-9-17/h3-11H,12-16H2,1-2H3	UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Arkansas for Medical Sciences Curated by ChEMBL					Assay Description Displacement of [3H]NMS from human M1 muscarinic receptor expressed in CHO-K1 cells				J Med Chem 56: 1693-703 (2013) Article DOI: 10.1021/jm301774u BindingDB Entry DOI: 10.7270/Q2765GN2
					More data for this Ligand-Target Pair
Muscarinic acetylcholine receptor M5 (Homo sapiens (Human))	BDBM50426256 (CHEMBL2312358) Show SMILES COc1ccc(CCOC(=O)C2=C(CCN(C)C2)c2ccccc2)cc1 |t:11| Show InChI InChI=1S/C22H25NO3/c1-23-14-12-20(18-6-4-3-5-7-18)21(16-23)22(24)26-15-13-17-8-10-19(25-2)11-9-17/h3-11H,12-16H2,1-2H3	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	30	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Arkansas for Medical Sciences Curated by ChEMBL					Assay Description Displacement of [3H]NMS from human M5 muscarinic receptor expressed in CHO-K1 cells				J Med Chem 56: 1693-703 (2013) Article DOI: 10.1021/jm301774u BindingDB Entry DOI: 10.7270/Q2765GN2
					More data for this Ligand-Target Pair