null

SMILES: Clc1ccc(s1)S(=O)(=O)c1cn(C2CCCNC2)c2ncccc12

InChI Key: InChIKey=XNJBCLZUQVQMEM-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50217883   

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))	BDBM50217883 (3-[(5-chlorothien-2-yl)sulfonyl]-1-piperidin-3-yl-...) Show SMILES Clc1ccc(s1)S(=O)(=O)c1cn(C2CCCNC2)c2ncccc12 |w:12.12| Show InChI InChI=1S/C16H16ClN3O2S2/c17-14-5-6-15(23-14)24(21,22)13-10-20(11-3-1-7-18-9-11)16-12(13)4-2-8-19-16/h2,4-6,8,10-11,18H,1,3,7,9H2	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.20	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 5HT6 expressed in HeLa cells				Bioorg Med Chem 15: 6208-26 (2007) Article DOI: 10.1016/j.bmc.2007.06.024 BindingDB Entry DOI: 10.7270/Q2HT2P2G
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 6 (Homo sapiens (Human))	BDBM50217883 (3-[(5-chlorothien-2-yl)sulfonyl]-1-piperidin-3-yl-...) Show SMILES Clc1ccc(s1)S(=O)(=O)c1cn(C2CCCNC2)c2ncccc12 |w:12.12| Show InChI InChI=1S/C16H16ClN3O2S2/c17-14-5-6-15(23-14)24(21,22)13-10-20(11-3-1-7-18-9-11)16-12(13)4-2-8-19-16/h2,4-6,8,10-11,18H,1,3,7,9H2	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Islamic Azad University Curated by ChEMBL					Assay Description Binding affinity to 5HT6 receptor				Eur J Med Chem 45: 3911-5 (2010) Article DOI: 10.1016/j.ejmech.2010.05.045 BindingDB Entry DOI: 10.7270/Q27945XK
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 6 (Homo sapiens (Human))	BDBM50217883 (3-[(5-chlorothien-2-yl)sulfonyl]-1-piperidin-3-yl-...) Show SMILES Clc1ccc(s1)S(=O)(=O)c1cn(C2CCCNC2)c2ncccc12 |w:12.12| Show InChI InChI=1S/C16H16ClN3O2S2/c17-14-5-6-15(23-14)24(21,22)13-10-20(11-3-1-7-18-9-11)16-12(13)4-2-8-19-16/h2,4-6,8,10-11,18H,1,3,7,9H2	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	98	n/a	n/a	n/a	n/a
Wyeth Research Curated by ChEMBL					Assay Description Agonist activity at human 5HT6 expressed in HeLa cells assessed as intracellular cAMP level by radioimmunoassay				Bioorg Med Chem 15: 6208-26 (2007) Article DOI: 10.1016/j.bmc.2007.06.024 BindingDB Entry DOI: 10.7270/Q2HT2P2G
					More data for this Ligand-Target Pair