BDBM404686 5-(4-{6-[(2S)-2-hydroxy-2- phenylacetamido]pyridazin-3- yl}butyl)-N-(2-phenylethyl)- 1,3,4-thiadiazole-2- carboxamide::US10344025, Example 25::US11370786, Example 25

SMILES O[C@H](C(=O)Nc1ccc(CCCCc2nnc(s2)C(=O)NCCc2ccccc2)nn1)c1ccccc1

InChI Key InChIKey=YMNIDGBOWUBKPL-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 = 404686   

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

US Patent
LigandPNGBDBM404686(5-(4-{6-[(2S)-2-hydroxy-2- phenylacetamido]pyridaz...)
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
LigandPNGBDBM404686(5-(4-{6-[(2S)-2-hydroxy-2- phenylacetamido]pyridaz...)
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