BDBM404717 5-[4-(4-{[(6-methylpyridin-3- yl)methyl]carbamoyl}-1H- 1,2,3-triazol-1-yl)butyl]-N-{[3- {(trifluoromethoxy)phenyl] methyl}-1,3,4-thiadiazole-2- carboxamide::US10344025, Example 61::US11370786, Example 61

SMILES Cc1ccc(CNC(=O)c2cn(CCCCc3nnc(s3)C(=O)NCc3cccc(OC(F)(F)F)c3)nn2)cn1

InChI Key InChIKey=FHOBDJBUUOJLLL-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 = 404717   

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

US Patent
LigandPNGBDBM404717(5-[4-(4-{[(6-methylpyridin-3- yl)methyl]carbamoyl}...)
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
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TargetGlutaminase kidney isoform, mitochondrial(Human)
The University of Texas System

US Patent
LigandPNGBDBM404717(5-[4-(4-{[(6-methylpyridin-3- yl)methyl]carbamoyl}...)
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
Go to US Patent