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SMILES: C[C@@H]1CCCN1CCCOc1ccc(cc1)-c1cccc(=O)n1C

InChI Key: InChIKey=CDBMTHSLJBFRAM-MRXNPFEDSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50358570   

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))	BDBM50358570 (CHEMBL1923731) Show SMILES C[C@@H]1CCCN1CCCOc1ccc(cc1)-c1cccc(=O)n1C |r| Show InChI InChI=1S/C20H26N2O2/c1-16-6-4-13-22(16)14-5-15-24-18-11-9-17(10-12-18)19-7-3-8-20(23)21(19)2/h3,7-12,16H,4-6,13-15H2,1-2H3/t16-/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	4.90	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))	BDBM50358570 (CHEMBL1923731) Show SMILES C[C@@H]1CCCN1CCCOc1ccc(cc1)-c1cccc(=O)n1C |r| Show InChI InChI=1S/C20H26N2O2/c1-16-6-4-13-22(16)14-5-15-24-18-11-9-17(10-12-18)19-7-3-8-20(23)21(19)2/h3,7-12,16H,4-6,13-15H2,1-2H3/t16-/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	21	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