1948-29-4 Usage
Description
H-GAMMA-GLU-GLY-OH, also known as a glutamyl-L-amino acid, is a compound formed by the formal condensation of the gamma-carboxy group of glutamic acid with the amino group of glycine. This molecule plays a significant role in various biological processes and has potential applications in different industries due to its unique structure and properties.
Uses
Used in Pharmaceutical Industry:
H-GAMMA-GLU-GLY-OH is used as a building block for the synthesis of various pharmaceutical compounds, such as peptides and proteins, for [application reason]. Its unique structure allows for the creation of complex molecules with specific functions and properties, making it a valuable component in drug development.
Used in Cosmetic Industry:
In the cosmetic industry, H-GAMMA-GLU-GLY-OH is used as an active ingredient in skincare products for [application reason]. Its ability to interact with proteins and other biomolecules can contribute to the development of products with anti-aging, moisturizing, and skin-repairing properties.
Used in Food Industry:
H-GAMMA-GLU-GLY-OH is used as a flavor enhancer and a component in the production of certain food additives for [application reason]. Its interaction with taste receptors can enhance the overall taste and flavor of various food products.
Used in Research and Development:
In the field of research and development, H-GAMMA-GLU-GLY-OH is used as a key compound in the study of protein structure, function, and interactions for [application reason]. Its unique properties make it an essential tool for understanding the complex mechanisms of biological systems and developing new therapeutic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 1948-29-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,4 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1948-29:
(6*1)+(5*9)+(4*4)+(3*8)+(2*2)+(1*9)=104
104 % 10 = 4
So 1948-29-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H12N2O5/c8-4(7(13)14)1-2-5(10)9-3-6(11)12/h4H,1-3,8H2,(H,9,10)(H,11,12)(H,13,14)
1948-29-4Relevant articles and documents
γ-Glutamyl-dipeptides: Easy tools to rapidly probe the stereoelectronic properties of the ionotropic glutamate receptor binding pocket
Tamborini, Lucia,Nicosia, Veronica,Conti, Paola,Dall'Oglio, Federica,De Micheli, Carlo,Nielsen, Birgitte,Jensen, Anders A.,Pickering, Darryl S.,Pinto, Andrea
, p. 8486 - 8492 (2016/11/28)
γ-Glutamyl-dipeptides, built by condensing the distal carboxylate of L-Glu (or D-Glu) onto a series of differently functionalized amino acids, were prepared and used as tools for rapidly probing the stereo-electronic properties of iGluRs, searching for subtype-selective ligands.
Synthesis of γ-Glutamylpeptides by γ-Glutamylcysteine Synthetase from Proteus mirabilis
Nakayama, Reiko,Kumagai, Hedehiko,Maruyama, Takashi,Tochikura, Tatsurokuro,Ueno, Tamio,Fukami, Hiroshi
, p. 2839 - 2846 (2007/10/02)
Syntheses of various γ-glutamylpeptides were examined taking use of the highly purified γ-glutamylcysteine synthetase from Proteus mirabilis.The accumulation of each peptide was measured after long time incubation, and good formation was observed in the synthesis of peptides of following amino acids, L-cysteine, L-α-aminobutyrate, L-serine, L-homoserine, glycine, L-alanine, L-norvaline, L-lysine, L-threonine, taurine and L-valine.Peptide syntheses were confirmed by analyses of the component amino acids, after hydrolysis of the peptides.The structure of the glutamylpeptides, especially the peptide-linkage at the γ-carbonyl residue of L-glutamate, was determined by mass spectrometry of the N-trifluoroacetyl methylester derivatives of the glutamylpeptides.Enzymatic synthesis of γ-glutamyl-L-α-aminobutyrate was also confirmed by PMR spectrometry in the comparison with chemically synthesized compound.
Synthesis of gamma-glutamyl peptides.
LE QUESNE,YOUNG
, p. 604 - 604 (2007/10/05)
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