BDBM50236843 CHEMBL4105377

SMILES: Cl.Cl.COc1ccc2n(cc(CN3CCNCC3)c2c1)S(=O)(=O)c1ccc(cc1)C(C)C

InChI Key: InChIKey=SXUMFJKMRHJVKR-UHFFFAOYSA-N

Data: 1 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 1 hit for monomerid = 50236843   

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))	BDBM50236843 (CHEMBL4105377) Show SMILES Cl.Cl.COc1ccc2n(cc(CN3CCNCC3)c2c1)S(=O)(=O)c1ccc(cc1)C(C)C Show InChI InChI=1S/C23H29N3O3S/c1-17(2)18-4-7-21(8-5-18)30(27,28)26-16-19(15-25-12-10-24-11-13-25)22-14-20(29-3)6-9-23(22)26/h4-9,14,16-17,24H,10-13,15H2,1-3H3	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	5.70	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Suven Life Sciences Ltd Curated by ChEMBL					Assay Description Displacement of [3H]-LSD from recombinant human 5-HT6 receptor expressed in HEK293 cells after 60 mins				J Med Chem 60: 1843-1859 (2017) Article DOI: 10.1021/acs.jmedchem.6b01662 BindingDB Entry DOI: 10.7270/Q27S7R1X
					More data for this Ligand-Target Pair