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SMILES N[C@@H](CCB(O)O)C(O)=O

InChI Key InChIKey=KSYFGBKMRXVJSG-VKHMYHEASA-N

PDB links: 1 PDB ID matches this monomer.

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50104413   

TargetGlutathione hydrolase 1 proenzyme(Homo sapiens (Human))TBA
LigandPNGBDBM50104413(CHEMBL87796 | Glutamyl-gamma-boronate analogue)copy SMILEScopy InChI
Affinity DataKi:  5.40nMMore data for this Ligand-Target Pair
TargetGlutathione hydrolase 1 proenzyme(Homo sapiens (Human))TBA
LigandPNGBDBM50104413(CHEMBL87796 | Glutamyl-gamma-boronate analogue)copy SMILEScopy InChI
Affinity DataKi:  25nMMore data for this Ligand-Target Pair
TargetGlutamyl-tRNA(Gln) amidotransferase subunit C(Streptococcus pyogenes serotype M1)
DuPont Pharmaceuticals Company

Curated by ChEMBL
LigandPNGBDBM50104413(CHEMBL87796 | Glutamyl-gamma-boronate analogue)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:In vitro inhibitory concentration against transferase activity of bacterial Glu-tRNA-Gln amidotransferase (Glu-AdT)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29K49H7PubMed
TargetGlutamyl-tRNA(Gln) amidotransferase subunit C(Streptococcus pyogenes serotype M1)
DuPont Pharmaceuticals Company

Curated by ChEMBL
LigandPNGBDBM50104413(CHEMBL87796 | Glutamyl-gamma-boronate analogue)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+3nMAssay Description:In vitro inhibitory concentration against Glutaminase activity of bacterial Glu-tRNA-Gln amidotransferase (Glu-AdT)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29K49H7PubMed