BDBM39364 MLS000039074::N-[4-[5-(2-furanyl)-1,3,4-oxadiazol-2-yl]phenyl]-2-(4-methylphenoxy)acetamide::N-[4-[5-(2-furyl)-1,3,4-oxadiazol-2-yl]phenyl]-2-(4-methylphenoxy)acetamide::N-[4-[5-(furan-2-yl)-1,3,4-oxadiazol-2-yl]phenyl]-2-(4-methylphenoxy)acetamide::N-[4-[5-(furan-2-yl)-1,3,4-oxadiazol-2-yl]phenyl]-2-(4-methylphenoxy)ethanamide::SMR000037084::cid_659595
SMILES Cc1ccc(OCC(=O)Nc2ccc(cc2)-c2nnc(o2)-c2ccco2)cc1
InChI Key InChIKey=RKZIMYYFNIGUHQ-UHFFFAOYSA-N
Data 3 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 3 hits for monomerid = 39364
Affinity DataIC50: 5.00E+4nMAssay Description:The HTS assay to identify Inhibitors of West Nile Virus (WNV) NS2bNS3 Proteinase was proposed by Dr Alex Strongin of the Burnham Institute XO1-MH0776...More data for this Ligand-Target Pair
TargetTyrosine-protein phosphatase non-receptor type 7(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
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Human)
Sejong University
Curated by ChEMBL
Sejong University
Curated by ChEMBL
Affinity DataIC50: 4.00E+4nMAssay Description:Inhibition of PI3KalphaMore data for this Ligand-Target Pair