BDBM54802 2-(N-(4-methoxyphenyl)sulfonylanilino)-N-(4-morpholin-4-ylsulfonylphenyl)acetamide::2-(N-(4-methoxyphenyl)sulfonylanilino)-N-(4-morpholinosulfonylphenyl)acetamide::2-(N-(4-methoxyphenyl)sulfonylanilino)-N-[4-(4-morpholinylsulfonyl)phenyl]acetamide::2-[(4-methoxyphenyl)sulfonyl-phenyl-amino]-N-(4-morpholin-4-ylsulfonylphenyl)ethanamide::MLS000581499::N~2~-[(4-methoxyphenyl)sulfonyl]-N~1~-[4-(4-morpholinylsulfonyl)phenyl]-N~2~-phenylglycinamide::SMR000200126::cid_2958242
SMILES COc1ccc(cc1)S(=O)(=O)N(CC(=O)Nc1ccc(cc1)S(=O)(=O)N1CCOCC1)c1ccccc1
InChI Key InChIKey=SJRUGQQDSSINLA-UHFFFAOYSA-N
Data 2 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 2 hits for monomerid = 54802
TargetKappa-type opioid receptor(Human)
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataIC50: 2.82E+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
TargetKappa-type opioid receptor(Human)
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataIC50: 4.04E+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
