BDBM405103 5-[3-fluoro-4-(4-{[(6-methylpyridin- 3-yl)methyl]carbamoyl}-1H-1,2,3- triazol-1-yl)butyl]-N-{[2-fluoro-5- (trifluoromethoxy)phenyl]methyl}- 1,3,4-thiadiazole-2-carboxamide::US10344025, Example 447::US11370786, Example 447
SMILES Cc1ccc(CNC(=O)c2cn(CC(F)CCc3nnc(s3)C(=O)NCc3cc(OC(F)(F)F)ccc3F)nn2)cn1
InChI Key InChIKey=CGJNPNXQZJGDGV-UHFFFAOYSA-N
Data 2 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 2 hits for monomerid = 405103
TargetGlutaminase kidney isoform, mitochondrial(Homo sapiens (Human))
Board of Regents, The University of Texas System
US Patent
Board of Regents, The University of Texas System
US Patent
Affinity DataIC50: <100nMAssay Description:The inhibition of purified recombinant human GAC by varying concentrations of inhibitors is assessed via a dual-coupled enzymatic assay. The glutamat...More data for this Ligand-Target Pair
TargetGlutaminase kidney isoform, mitochondrial(Homo sapiens (Human))
Board of Regents, The University of Texas System
US Patent
Board of Regents, The University of Texas System
US Patent
Affinity DataIC50: <100nMAssay Description:The inhibition of purified recombinant human GAC by varying concentrations of inhibitors is assessed via a dual-coupled enzymatic assay. The glutamat...More data for this Ligand-Target Pair