BDBM404689 N-benzyl-5-{4-[6-(2- phenylacetamido)pyridazin-3- yl]butyl}-1,3,4-thiadiazole-2- carboxamide::US10344025, Example 28::US11370786, Example 28

SMILES O=C(Cc1ccccc1)Nc1ccc(CCCCc2nnc(s2)C(=O)NCc2ccccc2)nn1

InChI Key InChIKey=OFFDHEGJSVLTEU-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 = 404689   

TargetGlutaminase kidney isoform, mitochondrial(Homo sapiens (Human))
Board Of Regents, The University Of Texas System

US Patent
LigandPNGBDBM404689(N-benzyl-5-{4-[6-(2- phenylacetamido)pyridazin-3- ...)
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
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetGlutaminase kidney isoform, mitochondrial(Homo sapiens (Human))
Board Of Regents, The University Of Texas System

US Patent
LigandPNGBDBM404689(N-benzyl-5-{4-[6-(2- phenylacetamido)pyridazin-3- ...)
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
Ligand InfoPC cidPC sid
In DepthDetails US Patent