BDBM50354201 CHEMBL1835995

SMILES: CC(C)N1CC[C@H](C1)N(C)C(=O)c1ccc(Cn2cnc3ccccc23)cc1

InChI Key: InChIKey=NHXHNDYJIBDZJX-HXUWFJFHSA-N

Data: 1 KI

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50354201   

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))	BDBM50354201 (CHEMBL1835995) Show SMILES CC(C)N1CC[C@H](C1)N(C)C(=O)c1ccc(Cn2cnc3ccccc23)cc1 |r| Show InChI InChI=1S/C23H28N4O/c1-17(2)26-13-12-20(15-26)25(3)23(28)19-10-8-18(9-11-19)14-27-16-24-21-6-4-5-7-22(21)27/h4-11,16-17,20H,12-15H2,1-3H3/t20-/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Inc. Curated by ChEMBL					Assay Description Displacement of [3H]-(R)alpha-methylhistamine from human histamine H3 receptor expressed in human HEK293T cells				Bioorg Med Chem Lett 21: 5957-60 (2011) Article DOI: 10.1016/j.bmcl.2011.07.061 BindingDB Entry DOI: 10.7270/Q2QN6753
					More data for this Ligand-Target Pair