BDBM50003353 2-Chloro-3-(1-methyl-1,2,5,6-tetrahydro-pyridin-3-yl)-pyrazine::CHEMBL131840

SMILES: CN1CCC=C(C1)c1nccnc1Cl

InChI Key: InChIKey=KRFOYOCNRILWAO-UHFFFAOYSA-N

Data: 2 IC50

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 = 50003353   

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)	BDBM50003353 (2-Chloro-3-(1-methyl-1,2,5,6-tetrahydro-pyridin-3-...) Show SMILES CN1CCC=C(C1)c1nccnc1Cl |c:4| Show InChI InChI=1S/C10H12ClN3/c1-14-6-2-3-8(7-14)9-10(11)13-5-4-12-9/h3-5H,2,6-7H2,1H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	PubMed	n/a	n/a	276	n/a	n/a	n/a	n/a	n/a	n/a
Lilly Research Laboratories Curated by ChEMBL					Assay Description In vitro binding affinity against rat hippocampus M1 receptor using [3H]-pirenzepine (Pz) as radioligand				J Med Chem 35: 4011-9 (1992) BindingDB Entry DOI: 10.7270/Q2KW5F1K
					More data for this Ligand-Target Pair
Muscarinic acetylcholine receptor M1 (RAT)	BDBM50003353 (2-Chloro-3-(1-methyl-1,2,5,6-tetrahydro-pyridin-3-...) Show SMILES CN1CCC=C(C1)c1nccnc1Cl |c:4| Show InChI InChI=1S/C10H12ClN3/c1-14-6-2-3-8(7-14)9-10(11)13-5-4-12-9/h3-5H,2,6-7H2,1H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	PubMed	n/a	n/a	>1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Lilly Research Laboratories Curated by ChEMBL					Assay Description Displacement of [3H]-pirenzepine (Pz) from rat hippocampus muscarinic acetylcholine receptor M1				J Med Chem 35: 4011-9 (1992) BindingDB Entry DOI: 10.7270/Q2KW5F1K
					More data for this Ligand-Target Pair