null

SMILES: O=S(=O)(NCc1ccccc1)c1ccc2C=CS(=O)(=O)c2c1

InChI Key: InChIKey=QCDOHNLYEMKNFZ-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50173863   

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
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50173863 (1,1-Dioxo-1H-1lambda*6*-benzo[b]thiophene-6-sulfon...) Show SMILES O=S(=O)(NCc1ccccc1)c1ccc2C=CS(=O)(=O)c2c1 |c:16| Show InChI InChI=1S/C15H13NO4S2/c17-21(18)9-8-13-6-7-14(10-15(13)21)22(19,20)16-11-12-4-2-1-3-5-12/h1-10,16H,11H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Università degli Studi di Firenze Curated by ChEMBL					Assay Description Inhibitory activity against human cloned Carbonic anhydrase II by the CO2 hydration method				Bioorg Med Chem Lett 15: 4872-6 (2005) Article DOI: 10.1016/j.bmcl.2005.04.078 BindingDB Entry DOI: 10.7270/Q2F18Z86
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50173863 (1,1-Dioxo-1H-1lambda*6*-benzo[b]thiophene-6-sulfon...) Show SMILES O=S(=O)(NCc1ccccc1)c1ccc2C=CS(=O)(=O)c2c1 |c:16| Show InChI InChI=1S/C15H13NO4S2/c17-21(18)9-8-13-6-7-14(10-15(13)21)22(19,20)16-11-12-4-2-1-3-5-12/h1-10,16H,11H2	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Università degli Studi di Firenze Curated by ChEMBL					Assay Description Inhibitory activity against catalytic domain of human cloned Carbonic anhydrase IX by the CO2 hydration method				Bioorg Med Chem Lett 15: 4872-6 (2005) Article DOI: 10.1016/j.bmcl.2005.04.078 BindingDB Entry DOI: 10.7270/Q2F18Z86
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50173863 (1,1-Dioxo-1H-1lambda*6*-benzo[b]thiophene-6-sulfon...) Show SMILES O=S(=O)(NCc1ccccc1)c1ccc2C=CS(=O)(=O)c2c1 |c:16| Show InChI InChI=1S/C15H13NO4S2/c17-21(18)9-8-13-6-7-14(10-15(13)21)22(19,20)16-11-12-4-2-1-3-5-12/h1-10,16H,11H2	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Università degli Studi di Firenze Curated by ChEMBL					Assay Description Inhibitory activity against human cloned Carbonic anhydrase I by the CO2 hydration method				Bioorg Med Chem Lett 15: 4872-6 (2005) Article DOI: 10.1016/j.bmcl.2005.04.078 BindingDB Entry DOI: 10.7270/Q2F18Z86
					More data for this Ligand-Target Pair