BDBM50038224 5-(2-Ethyl-2H-[1,2,3]triazol-4-yl)-1-methyl-1,2,3,6-tetrahydro-pyridine::CHEMBL131095

SMILES: CCn1ncc(n1)C1=CCCN(C)C1

InChI Key: InChIKey=IGYBMFIPDQRKSL-UHFFFAOYSA-N

Data: 1 KI  2 EC50

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 3 hits for monomerid = 50038224   

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)	BDBM50038224 (5-(2-Ethyl-2H-[1,2,3]triazol-4-yl)-1-methyl-1,2,3,...) Show SMILES CCn1ncc(n1)C1=CCCN(C)C1 |t:8| Show InChI InChI=1S/C10H16N4/c1-3-14-11-7-10(12-14)9-5-4-6-13(2)8-9/h5,7H,3-4,6,8H2,1-2H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	24	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
H. Lundbeck A/S Curated by ChEMBL					Assay Description In vitro binding affinity for muscarinic M1 receptor by displacing [3H]-Pirenzepine binding on rat brain homogenate.				J Med Chem 37: 4085-99 (1995) BindingDB Entry DOI: 10.7270/Q21N8066
					More data for this Ligand-Target Pair
Muscarinic acetylcholine receptor M1 (RAT)	BDBM50038224 (5-(2-Ethyl-2H-[1,2,3]triazol-4-yl)-1-methyl-1,2,3,...) Show SMILES CCn1ncc(n1)C1=CCCN(C)C1 |t:8| Show InChI InChI=1S/C10H16N4/c1-3-14-11-7-10(12-14)9-5-4-6-13(2)8-9/h5,7H,3-4,6,8H2,1-2H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	n/a	n/a	>1.20E+3	n/a	n/a	n/a	n/a
H. Lundbeck A/S Curated by ChEMBL					Assay Description M1 agonist activity estimated by rat superior cervical ganglion depolarization				J Med Chem 37: 4085-99 (1995) BindingDB Entry DOI: 10.7270/Q21N8066
					More data for this Ligand-Target Pair
Muscarinic acetylcholine receptor M2 (Homo sapiens (Human))	BDBM50038224 (5-(2-Ethyl-2H-[1,2,3]triazol-4-yl)-1-methyl-1,2,3,...) Show SMILES CCn1ncc(n1)C1=CCCN(C)C1 |t:8| Show InChI InChI=1S/C10H16N4/c1-3-14-11-7-10(12-14)9-5-4-6-13(2)8-9/h5,7H,3-4,6,8H2,1-2H3	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	n/a	n/a	>5.10E+4	n/a	n/a	n/a	n/a
H. Lundbeck A/S Curated by ChEMBL					Assay Description M2 agonist activity estimated by depression of isolated guinea pig left atrium				J Med Chem 37: 4085-99 (1995) BindingDB Entry DOI: 10.7270/Q21N8066
					More data for this Ligand-Target Pair