null

SMILES: C[C@@H]1CCCN1CCCOc1ccc(cc1)-c1ccc(=O)[nH]c1

InChI Key: InChIKey=SQQDRVSBXRKISM-OAHLLOKOSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50358568   

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))	BDBM50358568 (CHEMBL1923728) Show SMILES C[C@@H]1CCCN1CCCOc1ccc(cc1)-c1ccc(=O)[nH]c1 |r| Show InChI InChI=1S/C19H24N2O2/c1-15-4-2-11-21(15)12-3-13-23-18-8-5-16(6-9-18)17-7-10-19(22)20-14-17/h5-10,14-15H,2-4,11-13H2,1H3,(H,20,22)/t15-/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	7.70	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 expressed in CHO cells				Bioorg Med Chem Lett 21: 7076-80 (2011) Article DOI: 10.1016/j.bmcl.2011.09.091 BindingDB Entry DOI: 10.7270/Q26H4HVK
					More data for this Ligand-Target Pair
Histamine H3 receptor (Rattus norvegicus (rat))	BDBM50358568 (CHEMBL1923728) Show SMILES C[C@@H]1CCCN1CCCOc1ccc(cc1)-c1ccc(=O)[nH]c1 |r| Show InChI InChI=1S/C19H24N2O2/c1-15-4-2-11-21(15)12-3-13-23-18-8-5-16(6-9-18)17-7-10-19(22)20-14-17/h5-10,14-15H,2-4,11-13H2,1H3,(H,20,22)/t15-/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	9	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 expressed in CHO cells				Bioorg Med Chem Lett 21: 7076-80 (2011) Article DOI: 10.1016/j.bmcl.2011.09.091 BindingDB Entry DOI: 10.7270/Q26H4HVK
					More data for this Ligand-Target Pair