null

SMILES: CN(C)CCn1cc(c2nc(ccc12)C(C)=O)S(=O)(=O)c1cccc(F)c1

InChI Key: InChIKey=UNKWYRPAWUIZDJ-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50303162   

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))	BDBM50303162 (1-(1-(2-(dimethylamino)ethyl)-3-(3-fluorophenylsul...) Show SMILES CN(C)CCn1cc(c2nc(ccc12)C(C)=O)S(=O)(=O)c1cccc(F)c1 Show InChI InChI=1S/C19H20FN3O3S/c1-13(24)16-7-8-17-19(21-16)18(12-23(17)10-9-22(2)3)27(25,26)15-6-4-5-14(20)11-15/h4-8,11-12H,9-10H2,1-3H3	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	11.3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Wyeth Research Curated by ChEMBL					Assay Description Displacement of [3H]LSD from human HT6 receptor expressed in human HeLa cells				Bioorg Med Chem Lett 19: 6935-8 (2009) Article DOI: 10.1016/j.bmcl.2009.10.067 BindingDB Entry DOI: 10.7270/Q20K28PH
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 6 (Homo sapiens (Human))	BDBM50303162 (1-(1-(2-(dimethylamino)ethyl)-3-(3-fluorophenylsul...) Show SMILES CN(C)CCn1cc(c2nc(ccc12)C(C)=O)S(=O)(=O)c1cccc(F)c1 Show InChI InChI=1S/C19H20FN3O3S/c1-13(24)16-7-8-17-19(21-16)18(12-23(17)10-9-22(2)3)27(25,26)15-6-4-5-14(20)11-15/h4-8,11-12H,9-10H2,1-3H3	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	41	n/a	n/a	n/a	n/a	n/a	n/a
Wyeth Research Curated by ChEMBL					Assay Description Antagonistic activity at human HT6 receptor expressed in HeLa cells assessed as intracellular cAMP level by radioimmunoassay				Bioorg Med Chem Lett 19: 6935-8 (2009) Article DOI: 10.1016/j.bmcl.2009.10.067 BindingDB Entry DOI: 10.7270/Q20K28PH
					More data for this Ligand-Target Pair