BDBM50509924 CHEMBL4532574

SMILES: CC1CCCN1CCCOc1ccc2CCN(C)C(=O)c2c1

InChI Key: InChIKey=RNUFTULKGHQUKN-UHFFFAOYSA-N

Data: 2 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 2 hits for monomerid = 50509924   

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 H1 receptor (Cavia porcellus (domestic guinea pig))	BDBM50509924 (CHEMBL4532574) Show SMILES CC1CCCN1CCCOc1ccc2CCN(C)C(=O)c2c1 Show InChI InChI=1S/C18H26N2O2/c1-14-5-3-9-20(14)10-4-12-22-16-7-6-15-8-11-19(2)18(21)17(15)13-16/h6-7,13-14H,3-5,8-12H2,1-2H3	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	26	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Jiangsu Marine Resources Development Research Institute Curated by ChEMBL					Assay Description Displacement of [3H]-mepyramine from histamine H1 receptor in guinea pig cerebellum homogenates incubated for 60 mins by Cheng and Prusoff equation a...				Bioorg Med Chem Lett 29: 1492-1496 (2019) Article DOI: 10.1016/j.bmcl.2019.04.015
					More data for this Ligand-Target Pair
Histamine H3 receptor (Rattus norvegicus (rat))	BDBM50509924 (CHEMBL4532574) Show SMILES CC1CCCN1CCCOc1ccc2CCN(C)C(=O)c2c1 Show InChI InChI=1S/C18H26N2O2/c1-14-5-3-9-20(14)10-4-12-22-16-7-6-15-8-11-19(2)18(21)17(15)13-16/h6-7,13-14H,3-5,8-12H2,1-2H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	68	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Jiangsu Marine Resources Development Research Institute Curated by ChEMBL					Assay Description Displacement of [3H]-N-alpha-methylhistamine from histamine H3 receptor in rat cerebral cortex homogenates incubated for 60 mins by Cheng and Prusoff...				Bioorg Med Chem Lett 29: 1492-1496 (2019) Article DOI: 10.1016/j.bmcl.2019.04.015
					More data for this Ligand-Target Pair