BDBM50156222 CHEMBL3779974

SMILES: COc1ccc(cc1N1CCNCC1)S(=O)(=O)NCC1(CC1)c1cccc2ccc(Br)cc12

InChI Key: InChIKey=BAGMCZLXWXOPIX-UHFFFAOYSA-N

Data: 1 IC50

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 = 50156222   

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
5-hydroxytryptamine receptor 6 (Homo sapiens (Human))	BDBM50156222 (CHEMBL3779974) Show SMILES COc1ccc(cc1N1CCNCC1)S(=O)(=O)NCC1(CC1)c1cccc2ccc(Br)cc12 Show InChI InChI=1S/C25H28BrN3O3S/c1-32-24-8-7-20(16-23(24)29-13-11-27-12-14-29)33(30,31)28-17-25(9-10-25)22-4-2-3-18-5-6-19(26)15-21(18)22/h2-8,15-16,27-28H,9-14,17H2,1H3	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.20	n/a	n/a	n/a	n/a	n/a	n/a
Temple University Curated by ChEMBL					Assay Description Displacement of [3H]LSD from human 5-HT6 receptor expressed in CHO cell membranes after 120 mins by liquid scintillation counting method				ACS Med Chem Lett 7: 12-4 (2016) BindingDB Entry DOI: 10.7270/Q2Z89F8F
					More data for this Ligand-Target Pair