null

SMILES: Clc1ccc(OCCCCCCCN2CCCCCC2)cc1

InChI Key: InChIKey=RIFYNBIQUGNAIX-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 6 hits for monomerid = 50533180   

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
Histamine H3 receptor (Homo sapiens (Human))	BDBM50533180 (CHEMBL3747910) Show SMILES Clc1ccc(OCCCCCCCN2CCCCCC2)cc1 Show InChI InChI=1S/C19H30ClNO/c20-18-10-12-19(13-11-18)22-17-9-5-1-2-6-14-21-15-7-3-4-8-16-21/h10-13H,1-9,14-17H2	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	203	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Medical College Curated by ChEMBL					Assay Description Displacement of [3H]Nalpha-methylhistamine from human full length recombinant histamine H3 receptor expressed in HEK293 cell membranes after 90 mins ...				Bioorg Med Chem Lett 26: 4140-5 (2016) Article DOI: 10.1016/j.bmcl.2016.04.054
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50533180 (CHEMBL3747910) Show SMILES Clc1ccc(OCCCCCCCN2CCCCCC2)cc1 Show InChI InChI=1S/C19H30ClNO/c20-18-10-12-19(13-11-18)22-17-9-5-1-2-6-14-21-15-7-3-4-8-16-21/h10-13H,1-9,14-17H2	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	203	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Medical College Curated by ChEMBL					Assay Description Displacement of [3H]Nalpha-methylhistamine from human full length recombinant histamine H3 receptor expressed in HEK293 cell membranes after 90 mins ...				Bioorg Med Chem Lett 26: 4140-5 (2016) Article DOI: 10.1016/j.bmcl.2016.04.054
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50533180 (CHEMBL3747910) Show SMILES Clc1ccc(OCCCCCCCN2CCCCCC2)cc1 Show InChI InChI=1S/C19H30ClNO/c20-18-10-12-19(13-11-18)22-17-9-5-1-2-6-14-21-15-7-3-4-8-16-21/h10-13H,1-9,14-17H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.64E+3	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Medical College Curated by ChEMBL					Assay Description Inhibition of equine serum BChE using butyrylthiocholine chloride as substrate preincubated for 5 mins followed by substrate addition measured after ...				Bioorg Med Chem Lett 26: 4140-5 (2016) Article DOI: 10.1016/j.bmcl.2016.04.054
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50533180 (CHEMBL3747910) Show SMILES Clc1ccc(OCCCCCCCN2CCCCCC2)cc1 Show InChI InChI=1S/C19H30ClNO/c20-18-10-12-19(13-11-18)22-17-9-5-1-2-6-14-21-15-7-3-4-8-16-21/h10-13H,1-9,14-17H2	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.93E+3	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Medical College Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured after 5 m...				Bioorg Med Chem Lett 26: 4140-5 (2016) Article DOI: 10.1016/j.bmcl.2016.04.054
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50533180 (CHEMBL3747910) Show SMILES Clc1ccc(OCCCCCCCN2CCCCCC2)cc1 Show InChI InChI=1S/C19H30ClNO/c20-18-10-12-19(13-11-18)22-17-9-5-1-2-6-14-21-15-7-3-4-8-16-21/h10-13H,1-9,14-17H2	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.93E+3	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Medical College Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured after 5 m...				Bioorg Med Chem Lett 26: 4140-5 (2016) Article DOI: 10.1016/j.bmcl.2016.04.054
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50533180 (CHEMBL3747910) Show SMILES Clc1ccc(OCCCCCCCN2CCCCCC2)cc1 Show InChI InChI=1S/C19H30ClNO/c20-18-10-12-19(13-11-18)22-17-9-5-1-2-6-14-21-15-7-3-4-8-16-21/h10-13H,1-9,14-17H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.64E+3	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Medical College Curated by ChEMBL					Assay Description Inhibition of equine serum BChE using butyrylthiocholine chloride as substrate preincubated for 5 mins followed by substrate addition measured after ...				Bioorg Med Chem Lett 26: 4140-5 (2016) Article DOI: 10.1016/j.bmcl.2016.04.054
					More data for this Ligand-Target Pair