BDBM404922 1-(2-fluoro-4-(6-(2-(4-((1,1,1- trifluoropropan-2-yl)oxy)pyridin-2- yl)acetamido)pyridazin-3-yl)butyl)- N-methyl-1H-1,2,3-triazole-4- carboxamide::US10344025, Example 266::US11370786, Example 266

SMILES CNC(=O)c1cn(CC(F)CCc2ccc(NC(=O)Cc3cc(OC(C)C(F)(F)F)ccn3)nn2)nn1

InChI Key InChIKey=YARHNTKONKGJRM-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 = 404922   

TargetGlutaminase kidney isoform, mitochondrial(Human)
University Of Texas

US Patent
LigandChemical structure of BindingDB Monomer ID 404922BDBM404922(1-(2-fluoro-4-(6-(2-(4-((1,1,1- trifluoropropan-2-...)
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
LigandChemical structure of BindingDB Monomer ID 404922BDBM404922(1-(2-fluoro-4-(6-(2-(4-((1,1,1- trifluoropropan-2-...)
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