4-(γ-Glutamylamino)butanoic acid

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4-(γ-Glutamylamino)butanoic acid
Stereo, skeletal formula of 4-(γ-glutamylamino)butanoic acid (S)
Names
Preferred IUPAC name
2-Amino-5-[(4-hydroxy-4-oxobutyl)amino]-5-oxopentanoic acid[citation needed]
Systematic IUPAC name
4-Amino-5-((3-carboxypropyl)amino)-5-oxopentanoic acid[citation needed]
Other names
Identifiers
5105-96-4 S YesY
Abbreviations
2418119
ChEBI CHEBI:49260 YesY
ChEMBL ChEMBL269574 YesY
ChemSpider 315618 YesY
Jmol 3D model Interactive image
Interactive image
KEGG C15767 YesY
PubChem 355553
23724570 S
  • InChI=1S/C9H16N2O5/c10-6(9(15)16)3-4-7(12)11-5-1-2-8(13)14/h6H,1-5,10H2,(H,11,12)(H,13,14)(H,15,16) YesY
    Key: MKYPKZSGLSOGLL-UHFFFAOYSA-N YesY
  • NC(CCc(:[o]):[nH]CCCc(:[o]):[oH])c(:[o]):[oH]
  • NC(CCC(=O)NCCCC(O)=O)C(O)=O
Properties
C9H16N2O5
Molar mass 232.24 g·mol−1
log P −1.434
Acidity (pKa) 2.223
Basicity (pKb) 11.777
Related compounds
Related alkanoic acids
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
Infobox references

4-(γ-Glutamylamino)butanoic acid is molecule that consists of L-glutamate conjugated to γ-aminobutyric acid (GABA). It is the substrate of the enzyme γ-glutamyl-γ-aminobutyrate hydrolase, which is involved in the biosynthesis of polyamines.[2]

References

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