null

SMILES: C#CCn1ncc(n1)C1CCCNC1

InChI Key: InChIKey=FRGSXTHALSHQFX-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50038217   

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)	BDBM50038217 (3-(2-Prop-2-ynyl-2H-[1,2,3]triazol-4-yl)-piperidin...) Show SMILES C#CCn1ncc(n1)C1CCCNC1 Show InChI InChI=1S/C10H14N4/c1-2-6-14-12-8-10(13-14)9-4-3-5-11-7-9/h1,8-9,11H,3-7H2	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	84	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)	BDBM50038217 (3-(2-Prop-2-ynyl-2H-[1,2,3]triazol-4-yl)-piperidin...) Show SMILES C#CCn1ncc(n1)C1CCCNC1 Show InChI InChI=1S/C10H14N4/c1-2-6-14-12-8-10(13-14)9-4-3-5-11-7-9/h1,8-9,11H,3-7H2	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	140	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