BDBM58565 MLS001125540::N-(2-methyl-8-quinolinyl)benzenesulfonamide::N-(2-methyl-8-quinolyl)benzenesulfonamide::N-(2-methylquinolin-8-yl)benzenesulfonamide::SMR000658872::cid_2848041
SMILES Cc1ccc2cccc(NS(=O)(=O)c3ccccc3)c2n1
InChI Key InChIKey=IXWWCFNPCYOVOT-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 4 hits for monomerid = 58565
Affinity DataEC50: 1.50E+5nMAssay Description:Keywords: Group A streptococcus, GAS, streptokinase, expression, virulence, inhibition, dose response, EC50 Assay Overview: The goal of this assa...More data for this Ligand-Target Pair
Affinity DataIC50: 1.45E+4nMAssay Description:Inhibition recombinant human N-terminal 6His-tagged GLO1 (2 to 184 residues) expressed in Escherichia coli using MG as substrate preincubated for 15 ...More data for this Ligand-Target Pair
TargetType-1 angiotensin II receptor(Homo sapiens (Human))
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataIC50: 2.35E+3nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...More data for this Ligand-Target Pair
TargetApelin receptor(Homo sapiens (Human))
Sanford-Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Sanford-Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataIC50: 5.38E+3nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford- Sanford-Burnham Medical Research Institute(SBMRI, San...More data for this Ligand-Target Pair