null

SMILES: O=NC1c2ccccc2-c2ccc(OCCN3CCCCC3)cc12

InChI Key: InChIKey=ITJCJWRMZNXRFC-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50117887   

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))	BDBM50117887 (2-(2-Piperidin-1-yl-ethoxy)-fluoren-9-one oxime | ...) Show SMILES O=NC1c2ccccc2-c2ccc(OCCN3CCCCC3)cc12 Show InChI InChI=1S/C20H22N2O2/c23-21-20-18-7-3-2-6-16(18)17-9-8-15(14-19(17)20)24-13-12-22-10-4-1-5-11-22/h2-3,6-9,14,20H,1,4-5,10-13H2	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	45	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Schering Plough Research Institute Curated by ChEMBL					Assay Description In vitro binding affinity against Histamine H3 receptor				Bioorg Med Chem Lett 12: 2643-6 (2002) BindingDB Entry DOI: 10.7270/Q26Q1WMX
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50117887 (2-(2-Piperidin-1-yl-ethoxy)-fluoren-9-one oxime | ...) Show SMILES O=NC1c2ccccc2-c2ccc(OCCN3CCCCC3)cc12 Show InChI InChI=1S/C20H22N2O2/c23-21-20-18-7-3-2-6-16(18)17-9-8-15(14-19(17)20)24-13-12-22-10-4-1-5-11-22/h2-3,6-9,14,20H,1,4-5,10-13H2	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	65	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Schering Plough Research Institute Curated by ChEMBL					Assay Description In vitro binding affinity for Histamine H3 receptor				Bioorg Med Chem Lett 12: 2643-6 (2002) BindingDB Entry DOI: 10.7270/Q26Q1WMX
					More data for this Ligand-Target Pair