null

SMILES: NS(=O)(=O)c1cc2NC(=O)CS(=O)(=O)c2s1

InChI Key: InChIKey=BPWMBDNQLXXVNB-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50043907   

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))	BDBM50043907 (2,4,4-Trioxo-1,2,3,4-tetrahydro-4lambda*6*-thieno[...) Show SMILES NS(=O)(=O)c1cc2NC(=O)CS(=O)(=O)c2s1 Show InChI InChI=1S/C6H6N2O5S3/c7-16(12,13)5-1-3-6(14-5)15(10,11)2-4(9)8-3/h1H,2H2,(H,8,9)(H2,7,12,13)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	2.90	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Tested for ability to compete with dansylamide for binding to human erythrocyte carbonic-anhydrase-II (HCA-II)				J Med Chem 37: 240-7 (1994) BindingDB Entry DOI: 10.7270/Q2N29XKD
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50043907 (2,4,4-Trioxo-1,2,3,4-tetrahydro-4lambda*6*-thieno[...) Show SMILES NS(=O)(=O)c1cc2NC(=O)CS(=O)(=O)c2s1 Show InChI InChI=1S/C6H6N2O5S3/c7-16(12,13)5-1-3-6(14-5)15(10,11)2-4(9)8-3/h1H,2H2,(H,8,9)(H2,7,12,13)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	3.70	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Tested for ability to inhibit human erythrocyte carbonic-anhydrase-II- (HCA II) catalyzed carbon dioxide hydration				J Med Chem 37: 240-7 (1994) BindingDB Entry DOI: 10.7270/Q2N29XKD
					More data for this Ligand-Target Pair