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]
Names | |
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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
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Identifiers | |
3D model (JSmol)
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Abbreviations |
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2418119 | |
ChEBI | |
ChEMBL | |
ChemSpider | |
KEGG | |
PubChem CID
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CompTox Dashboard (EPA)
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Properties | |
C9H16N2O5 | |
Molar mass | 232.236 g·mol−1 |
log P | −1.434 |
Acidity (pKa) | 2.223 |
Basicity (pKb) | 11.777 |
Related compounds | |
Related alkanoic acids
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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References
edit- ^ "NSC609423 - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 26 March 2005. Identification. Retrieved 8 July 2012.
- ^ Kurihara S, Oda S, Kato K, Kim HG, Koyanagi T, Kumagai H, Suzuki H (2005). "A novel putrescine utilization pathway involves gamma-glutamylated intermediates of Escherichia coli K-12". J. Biol. Chem. 280 (6): 4602–8. doi:10.1074/jbc.M411114200. PMID 15590624.4602-8&rft.date=2005&rft_id=info:doi/10.1074/jbc.M411114200&rft_id=info:pmid/15590624&rft.aulast=Kurihara&rft.aufirst=S&rft.au=Oda, S&rft.au=Kato, K&rft.au=Kim, HG&rft.au=Koyanagi, T&rft.au=Kumagai, H&rft.au=Suzuki, H&rft_id=https://doi.org/10.1074%2Fjbc.M411114200&rfr_id=info:sid/en.wikipedia.org:4-(γ-Glutamylamino)butanoic acid" class="Z3988">