BDBM76434 5-(2-Chloro-phenyl)-furan-2-carboxylic acid thiazol-2-ylamide::5-(2-chlorophenyl)-N-(1,3-thiazol-2-yl)furan-2-carboxamide::5-(2-chlorophenyl)-N-(2-thiazolyl)-2-furancarboxamide::5-(2-chlorophenyl)-N-thiazol-2-yl-2-furamide::MLS000557786::SMR000178404::cid_1084407
SMILES Clc1ccccc1-c1ccc(o1)C(=O)Nc1nccs1
InChI Key InChIKey=JVPTXRIDTOXHSR-UHFFFAOYSA-N
Data 4 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 4 hits for monomerid = 76434
Affinity DataIC50: 2.20E+4nMAssay 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
TargetSentrin-specific protease 8(Human)
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataIC50: 2.51E+4nMAssay 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
TargetSentrin-specific protease 6(Human)
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataIC50: 1.00E+5nMAssay 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
Affinity DataIC50: 1.83E+4nMAssay Description:Inhibition of alpha glucosidase (unknown origin)More data for this Ligand-Target Pair
