null

SMILES: CC(C)N1CCN(CC1)C(=O)c1ccc(cc1)-c1ccc(=O)n(C)n1

InChI Key: InChIKey=QDPDRXXIJJDDNM-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50352805   

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))	BDBM50352805 (CHEMBL1823409) Show SMILES CC(C)N1CCN(CC1)C(=O)c1ccc(cc1)-c1ccc(=O)n(C)n1 Show InChI InChI=1S/C19H24N4O2/c1-14(2)22-10-12-23(13-11-22)19(25)16-6-4-15(5-7-16)17-8-9-18(24)21(3)20-17/h4-9,14H,10-13H2,1-3H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	167	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Cephalon Inc. Curated by ChEMBL					Assay Description Displacement of [3H]-NAMH from human histamine H3 receptor				Bioorg Med Chem Lett 21: 5543-6 (2011) Article DOI: 10.1016/j.bmcl.2011.06.094 BindingDB Entry DOI: 10.7270/Q2QF8TW7
					More data for this Ligand-Target Pair
Histamine H3 receptor (Rattus norvegicus (rat))	BDBM50352805 (CHEMBL1823409) Show SMILES CC(C)N1CCN(CC1)C(=O)c1ccc(cc1)-c1ccc(=O)n(C)n1 Show InChI InChI=1S/C19H24N4O2/c1-14(2)22-10-12-23(13-11-22)19(25)16-6-4-15(5-7-16)17-8-9-18(24)21(3)20-17/h4-9,14H,10-13H2,1-3H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	185	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Cephalon Inc. Curated by ChEMBL					Assay Description Displacement of [3H]-NAMH from rat histamine H3 receptor				Bioorg Med Chem Lett 21: 5543-6 (2011) Article DOI: 10.1016/j.bmcl.2011.06.094 BindingDB Entry DOI: 10.7270/Q2QF8TW7
					More data for this Ligand-Target Pair