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SMILES: CC[C@@H]1[C@@H](Cc2cncn2C)CNC1=O

InChI Key: InChIKey=LWYKXKGPFMXVIY-WCBMZHEXSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50008067   

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)	BDBM50008067 (3-Ethyl-4-(3-methyl-3H-imidazol-4-ylmethyl)-pyrrol...) Show SMILES CC[C@@H]1[C@@H](Cc2cncn2C)CNC1=O Show InChI InChI=1S/C11H17N3O/c1-3-10-8(5-13-11(10)15)4-9-6-12-7-14(9)2/h6-8,10H,3-5H2,1-2H3,(H,13,15)/t8-,10+/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	800	n/a	n/a	n/a	n/a	n/a	n/a
Sandoz Pharma Ltd. Curated by ChEMBL					Assay Description Ability to displace [3H]cis--2-methyl-5-((dimethylamino)methyl)-1,3-di oxolane from muscarinic acetylcholine receptor in rat cortical tissue.				J Med Chem 35: 15-27 (1992) BindingDB Entry DOI: 10.7270/Q29022RV
					More data for this Ligand-Target Pair
Muscarinic acetylcholine receptor M1 (RAT)	BDBM50008067 (3-Ethyl-4-(3-methyl-3H-imidazol-4-ylmethyl)-pyrrol...) Show SMILES CC[C@@H]1[C@@H](Cc2cncn2C)CNC1=O Show InChI InChI=1S/C11H17N3O/c1-3-10-8(5-13-11(10)15)4-9-6-12-7-14(9)2/h6-8,10H,3-5H2,1-2H3,(H,13,15)/t8-,10+/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	9.95E+3	n/a	n/a	n/a	n/a	n/a	n/a
Sandoz Pharma Ltd. Curated by ChEMBL					Assay Description Ability to displace [3H]-pirenzepine (pir) from muscarinic acetylcholine receptor M1 in rat cortical tissue.				J Med Chem 35: 15-27 (1992) BindingDB Entry DOI: 10.7270/Q29022RV
					More data for this Ligand-Target Pair