BDBM405258 5-(4-(6-acetamidopyridazin-3-yl) butyl)-N-((5-(trifluoromethyl) pyridin-3-yl)methyl)-1,3,4- thiadiazole-2-carboxamide::US10344025, Example 602::US11370786, Example 602

SMILES CC(=O)Nc1ccc(CCCCc2nnc(s2)C(=O)NCc2cncc(c2)C(F)(F)F)nn1

InChI Key InChIKey=HIFUSFJFJROGSQ-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 = 405258   

TargetGlutaminase kidney isoform, mitochondrial(Human)
University Of Texas

US Patent
LigandPNGBDBM405258(5-(4-(6-acetamidopyridazin-3-yl) butyl)-N-((5-(tri...)
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

TargetGlutaminase kidney isoform, mitochondrial(Human)
University Of Texas

US Patent
LigandPNGBDBM405258(5-(4-(6-acetamidopyridazin-3-yl) butyl)-N-((5-(tri...)
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