BDBM50171289 Benzenemethanesulfonyl fluoride::CHEMBL190503::PMSF::Phenylmethanesulfonyl fluoride::alpha-toluenesulfonyl fluoride::alpha-toluenesulphonyl fluoride::phenylmethylsulfonyl fluoride
SMILES FS(=O)(=O)Cc1ccccc1
InChI Key InChIKey=YBYRMVIVWMBXKQ-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 7 hits for monomerid = 50171289
Affinity DataKi: 1.00E+4nMAssay Description:Competitive inhibition of trypsin (unknown origin) using N-succinyl-phenylalanine-p-nitroanilide as substrate incubated for 20 mins prior to substrat...More data for this Ligand-Target Pair
Affinity DataIC50: 9.52E+4nMAssay Description:Inhibition of human neutrophil elastase after 30 mins by ELISAMore data for this Ligand-Target Pair
Affinity DataIC50: 5.22E+4nMAssay Description:Inhibition of human leukocyte elastase after 2 mins by ELISAMore data for this Ligand-Target Pair
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Northeastern University
Curated by ChEMBL
Northeastern University
Curated by ChEMBL
Affinity DataIC50: 833nMAssay Description:Inhibition of rat histidine tagged FAAH expressed in Escherichia coli by coumarin ester substrate fluorescence assayMore data for this Ligand-Target Pair
Affinity DataIC50: 1.10E+5nMAssay Description:Inhibition of trypsin (unknown origin) using BApNA as substrate incubated for 15 min prior to substrate addition measured after 30 min by UV/VIS spec...More data for this Ligand-Target Pair
Affinity DataIC50: 1.92E+4nMAssay Description:Inhibition of human PR3 using D-DY-FRET as substrate after 30 mins by HPLC analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 1.30E+4nMAssay Description:Irreversible inhibition of fatty acid amide hydrolaseMore data for this Ligand-Target Pair