BDBM405232 1-(2-fluoro-4-(5-(2-(1-methyl-1H- imidazol-4-yl)acetamido)-1,3,4- thiadiazol-2-yl)butyl)-N-(2-fluoro-5- (trifluoromethoxy)benzyl)-1H-1,2,3- triazole-4-carboxamide::US10344025, Example 576::US11370786, Example 576

SMILES Cn1cnc(CC(=O)Nc2nnc(CCC(F)Cn3cc(nn3)C(=O)NCc3cc(OC(F)(F)F)ccc3F)s2)c1

InChI Key InChIKey=CTXONQFPKYYPEW-UHFFFAOYSA-N

Data  2 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 405232   

TargetGlutaminase kidney isoform, mitochondrial(Human)
The University of Texas System

US Patent
LigandPNGBDBM405232(1-(2-fluoro-4-(5-(2-(1-methyl-1H- imidazol-4-yl)ac...)
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
In Depth
Date in BDB:
6/8/2020
Entry Details
US Patent

TargetGlutaminase kidney isoform, mitochondrial(Human)
The University of Texas System

US Patent
LigandPNGBDBM405232(1-(2-fluoro-4-(5-(2-(1-methyl-1H- imidazol-4-yl)ac...)
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
In Depth
Date in BDB:
9/25/2022
Entry Details
US Patent