BDBM50156228 CHEMBL3781179

SMILES: COc1ccc(cc1N1CCN(C)CC1)S(=O)(=O)NCCc1cccc2ccccc12

InChI Key: InChIKey=PTKLNFTZLGQRAY-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 = 50156228   

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))	BDBM50156228 (CHEMBL3781179) Show SMILES COc1ccc(cc1N1CCN(C)CC1)S(=O)(=O)NCCc1cccc2ccccc12 Show InChI InChI=1S/C24H29N3O3S/c1-26-14-16-27(17-15-26)23-18-21(10-11-24(23)30-2)31(28,29)25-13-12-20-8-5-7-19-6-3-4-9-22(19)20/h3-11,18,25H,12-17H2,1-2H3	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	0.920	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