null

SMILES: Fc1ccc(cc1)S(=O)(=O)n1cc(C2=CCCNC2)c2ccccc12

InChI Key: InChIKey=PKSXYHMBORWHAI-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50172301   

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))	BDBM50172301 (1-(4-Fluoro-benzenesulfonyl)-3-(1,2,5,6-tetrahydro...) Show SMILES Fc1ccc(cc1)S(=O)(=O)n1cc(C2=CCCNC2)c2ccccc12 |t:14| Show InChI InChI=1S/C19H17FN2O2S/c20-15-7-9-16(10-8-15)25(23,24)22-13-18(14-4-3-11-21-12-14)17-5-1-2-6-19(17)22/h1-2,4-10,13,21H,3,11-12H2	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	10.5	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 cloned human 5-hydroxytryptamine 6 receptor expressed in HeLa cells				Bioorg Med Chem Lett 15: 4780-5 (2005) Article DOI: 10.1016/j.bmcl.2005.07.028 BindingDB Entry DOI: 10.7270/Q2RN37DD
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 6 (Homo sapiens (Human))	BDBM50172301 (1-(4-Fluoro-benzenesulfonyl)-3-(1,2,5,6-tetrahydro...) Show SMILES Fc1ccc(cc1)S(=O)(=O)n1cc(C2=CCCNC2)c2ccccc12 |t:14| Show InChI InChI=1S/C19H17FN2O2S/c20-15-7-9-16(10-8-15)25(23,24)22-13-18(14-4-3-11-21-12-14)17-5-1-2-6-19(17)22/h1-2,4-10,13,21H,3,11-12H2	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	345	n/a	n/a	n/a	n/a
Wyeth Research Curated by ChEMBL					Assay Description Effective concentration for cAMP production in HeLa cells expressing human 5-HT6 receptors				Bioorg Med Chem Lett 15: 4780-5 (2005) Article DOI: 10.1016/j.bmcl.2005.07.028 BindingDB Entry DOI: 10.7270/Q2RN37DD
					More data for this Ligand-Target Pair