null

SMILES: CCC(C)(C)c1ccc(OCCCN2CCC(C)CC2)cc1

InChI Key: InChIKey=GIYYXNQHYAZKNE-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50507164   

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))	BDBM50507164 (CHEMBL4473751) Show SMILES CCC(C)(C)c1ccc(OCCCN2CCC(C)CC2)cc1 Show InChI InChI=1S/C20H33NO/c1-5-20(3,4)18-7-9-19(10-8-18)22-16-6-13-21-14-11-17(2)12-15-21/h7-10,17H,5-6,11-16H2,1-4H3	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	147	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Medical College Curated by ChEMBL					Assay Description Displacement of [3H]-N-alpha-methylhistamine from human H3 receptor expressed in CHO-K1 cell membranes after 60 mins by microbeta2 scintillation coun...				Bioorg Med Chem Lett 28: 3596-3600 (2018) Article DOI: 10.1016/j.bmcl.2018.10.048
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] B (Homo sapiens (Human))	BDBM50507164 (CHEMBL4473751) Show SMILES CCC(C)(C)c1ccc(OCCCN2CCC(C)CC2)cc1 Show InChI InChI=1S/C20H33NO/c1-5-20(3,4)18-7-9-19(10-8-18)22-16-6-13-21-14-11-17(2)12-15-21/h7-10,17H,5-6,11-16H2,1-4H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.07E+3	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Medical College Curated by ChEMBL					Assay Description Inhibition of human MAO-B expressed in baculovirus infected BTI insect cells using p-tyramine as substrate preincubated for 30 mins followed by subst...				Bioorg Med Chem Lett 28: 3596-3600 (2018) Article DOI: 10.1016/j.bmcl.2018.10.048
					More data for this Ligand-Target Pair