CAS 21064-18-6

glu-ala

Description:

The chemical substance known as "glu-ala," with the CAS number 21064-18-6, is a dipeptide composed of the amino acids glutamic acid (Glu) and alanine (Ala). This compound is characterized by its specific sequence, where glutamic acid is linked to alanine through a peptide bond. Dipeptides like glu-ala play significant roles in biological systems, serving as building blocks for proteins and influencing various metabolic processes. The presence of the carboxylic acid group from glutamic acid contributes to the molecule's overall polarity and solubility in water, while the non-polar side chain of alanine provides hydrophobic characteristics. Glu-ala can participate in various biochemical reactions and may have implications in nutrition and health, particularly in relation to protein synthesis and cellular functions. Additionally, its structural properties can influence its interaction with enzymes and receptors, making it a subject of interest in biochemical research. Overall, glu-ala exemplifies the complexity and functionality of peptides in biological systems.

Formula: C₈H₁₄N₂O₅

InChI: InChI=1/C8H14N2O5/c1-4(8(14)15)10-7(13)5(9)2-3-6(11)12/h4-5H,2-3,9H2,1H3,(H,10,13)(H,11,12)(H,14,15)

InChI key: InChIKey=JZDHUJAFXGNDSB-WHFBIAKZSA-N

SMILES: C([C@H](CCC(O)=O)N)(N[C@H](C(O)=O)C)=O

Synonyms:

• 446: PN: WO2005081628 SEQID: 1555 claimed protein
• 59: PN: WO2014102101 SEQID: 359 claimed protein
• 59: PN: WO2014102104 SEQID: 158 claimed protein
• <span class="text-smallcaps">L</smallcap>-Alanine, <smallcap>L</span>-α-glutamyl-
• <span class="text-smallcaps">L</smallcap>-Alanine, N-<smallcap>L</span>-α-glutamyl-
• <span class="text-smallcaps">L</smallcap>-Glutamyl-<smallcap>L</span>-alanine
• <span class="text-smallcaps">L</smallcap>-α-Glutamyl-<smallcap>L</span>-alanine
• Alpha-Glutamylalanine
• Glutamylalanine
• Glutaramic acid, 4-amino-N-(1-carboxyethyl)-
• Glutaramic acid, 4-amino-N-(1-carboxyethyl)-, stereoisomer
• H-Glu-Ala-OH
• NSC 334200
• α-<span class="text-smallcaps">L</smallcap>-Glutamyl-<smallcap>L</span>-alanine
• α-Glu-Ala
• α-Glutamylalanine
• L-α-Glutamyl-L-alanine
• L-Alanine, N-L-α-glutamyl-

H-Glu-Ala-OH

CAS: 21064-18-6

Bachem ID: 4001473.

Formula: C₈H₁₄N₂O₅

Purity: > 99%

Color and Shape: White Powder

Molecular weight: 218.21

Ref: 01-4001473

(S)-4-Amino-5-(((S)-1-carboxyethyl)amino)-5-oxopentanoic acid

CAS: 21064-18-6

(S)-4-Amino-5-(((S)-1-carboxyethyl)amino)-5-oxopentanoic acid

Purity: 98%

Molecular weight: 218.21g/mol

Ref: 54-OR1074090

Alanyl Glutamine Impurity 32

CAS: 21064-18-6

Formula: C₈H₁₄N₂O₅

Molecular weight: 218.21

Ref: 4Z-G-3042

4-​Amino-​N-​(1-​carboxyethyl)​-glutaramic Acid

CAS: 21064-18-6

Formula: C₈H₁₄N₂O₅

Molecular weight: 218.21

Ref: ST-EA-CP-G54017

H-Glu-Ala-OH

CAS: 21064-18-6

H-Glu-Ala-OH is a human protein that belongs to the family of glycosylated proteins. It is expressed in the cells of the ovary and is a member of the insulin-like growth factor (IGF) superfamily. H-Glu-Ala-OH binds to lectins in mammalian cells, which may be due to its sulfoxide group. This protein has been shown to have dehydrogenase activity and polymerase chain reaction (PCR) amplification properties. H-Glu-Ala-OH has also been shown to inhibit growth in cell culture and promote apoptosis, which may be due to its ability to regulate IGF levels in mammalian cells.br>br>
br>br>
This protein is found at high levels in ovarian cancer cells and serum from patients with ovarian cancer. The sequence of this protein has been determined using mass spectrometry analysis on ovary extracts and on cDNA derived from human embryonic kidney (

Formula: C₈H₁₄N₂O₅

Purity: Min. 95 Area-%

Color and Shape: Powder

Molecular weight: 218.21 g/mol

Ref: 3D-FG108028