BDBM50410330 CHEMBL191405

SMILES: CCN(CC)Cc1ccc(OC2CCN(CC2)C(C)C)cc1

InChI Key: InChIKey=OHASLHKANGQFTI-UHFFFAOYSA-N

Data: 1 KI  1 Kd

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 2 hits for monomerid = 50410330   

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))	BDBM50410330 (CHEMBL191405) Show SMILES CCN(CC)Cc1ccc(OC2CCN(CC2)C(C)C)cc1 Show InChI InChI=1S/C19H32N2O/c1-5-20(6-2)15-17-7-9-18(10-8-17)22-19-11-13-21(14-12-19)16(3)4/h7-10,16,19H,5-6,11-15H2,1-4H3	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.23	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Mean binding affinity for human H3 receptor				J Med Chem 48: 2229-38 (2005) Article DOI: 10.1021/jm049212n BindingDB Entry DOI: 10.7270/Q2GB258T
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50410330 (CHEMBL191405) Show SMILES CCN(CC)Cc1ccc(OC2CCN(CC2)C(C)C)cc1 Show InChI InChI=1S/C19H32N2O/c1-5-20(6-2)15-17-7-9-18(10-8-17)22-19-11-13-21(14-12-19)16(3)4/h7-10,16,19H,5-6,11-15H2,1-4H3	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	0.468	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Mean functional activity against human H3 receptor				J Med Chem 48: 2229-38 (2005) Article DOI: 10.1021/jm049212n BindingDB Entry DOI: 10.7270/Q2GB258T
					More data for this Ligand-Target Pair