1948-29-4

1948-29-4 structure

Name: H-Glu(Gly-OH)-OH
Chemical Name: 2-amino-5-(carboxymethylamino)-5-oxopentanoic acid
CAS Number: 1948-29-4
Molecular Formula: C₇H₁₂N₂O₅
Molecular Weight: 204.18100
Catalog: Research Areas Metabolic Disease
Create Date: 2016-02-09 07:10:47
Modify Date: 2024-01-09 20:41:46
γ-Glu-Gly, a γ-glutamyl dipeptide, is a human lipid metabolite.γ-Glu-Gly has a similar structure to GABA (γ-aminobutyric acid) and can act as an antagonist of excitatory amino acids[1][2][3].

Name	2-amino-5-(carboxymethylamino)-5-oxopentanoic acid
Synonyms	H-g-Glu-Gly-OH H-GLU(GLY)-OH L-Y-GLUTAMYL-GLYCINE H-GLU(GLY-OH)-OH H-Glu-Gly-OH H-γ-Glu-Gly-OH

Description	γ-Glu-Gly, a γ-glutamyl dipeptide, is a human lipid metabolite.γ-Glu-Gly has a similar structure to GABA (γ-aminobutyric acid) and can act as an antagonist of excitatory amino acids[1][2][3].
Related Catalog	Research Areas >> Metabolic Disease
Target	Human Endogenous Metabolite
In Vitro	γ-Glu-Gly is a key component that influence the flavor of mature cheese. In S. cerevisiae, γ-Glutamyltransferase (GGT) produces two γ-glutamyl peptides, γ-Glu-Glu and γ-Glu-Gly[1].
References	[1]. Kit-Yi Leung, et al. Regulation of glycine metabolism by the glycine cleavage system and conjugation pathway in mouse models of non-ketotic hyperglycinemia. J Inherit Metab Dis. 2020 Nov;43(6):1186-1198. [2]. Sonu Yadav, et al. Metabolomics shows the Australian dingo has a unique plasma profile. Sci Rep. 2021 Mar 4;11(1):5245. [3]. Olga A Sofyanovich, et al. Multiple pathways for the formation of the γ-glutamyl peptides γ-glutamyl-valine and γ- glutamyl-valyl-glycine in Saccharomyces cerevisiae. PLoS One. 2019 May 9;14(5):e0216622.

HS Code	2924199090

Precursor 0
DownStream 2
56-86-0 56-40-6

HS Code	2924199090
Summary	2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%