CAS 37460-22-3

L-Alanine,L-alanylglycyl-

Description:

L-Alanine, L-alanylglycyl- is a dipeptide composed of the amino acids L-alanine and glycine. It is characterized by its structure, which features a peptide bond linking the carboxyl group of L-alanine to the amino group of glycine. This compound is typically white to off-white in appearance and is soluble in water, making it suitable for various biochemical applications. L-alanylglycine can play a role in protein synthesis and may be involved in metabolic processes. Its properties include being non-toxic and having a relatively low molecular weight, which facilitates its absorption and utilization in biological systems. Additionally, it may exhibit specific biological activities, such as acting as a neurotransmitter or influencing metabolic pathways. As with many peptides, its stability can be affected by environmental factors such as pH and temperature, which are important considerations in its storage and application in research or therapeutic contexts.

Formula: C₈H₁₅N₃O₄

Synonyms:

• Alanine,N-(N-alanylglycyl)- (7CI)
• L-Alanine, N-(N-L-alanylglycyl)-
• 499: PN: WO0104316PAGE: 49 claimed protein
• 9: PN: US20050260564 PAGE: 29 claimed protein
• L-Alanylglycyl-L-alanine

H-Ala-Gly-Ala-OH

CAS: 37460-22-3

Bachem ID: 4013351.

Formula: C₈H₁₅N₃O₄

Purity: > 99%

Color and Shape: White Powder

Molecular weight: 217.23

Ref: 01-4013351

(S)-2-(2-((S)-2-Aminopropanamido)acetamido)propanoic acid

CAS: 37460-22-3

(S)-2-(2-((S)-2-Aminopropanamido)acetamido)propanoic acid

Purity: 97%

Molecular weight: 217.22g/mol

Ref: 54-OR1069326

H-Ala-Gly-Ala-OH

CAS: 37460-22-3

H-Ala-Gly-Ala-OH is a small molecule that regulates the replication of viruses. It was discovered by x-ray crystallography and has been shown to inhibit the replication of viruses in cell culture. H-Ala-Gly-Ala-OH effectively inhibits viral replication by binding to the protein that is required for viral RNA synthesis. This molecule also affects other cellular processes, such as regulating gene expression and DNA repair. The molecular orbital energies have been calculated using density functional theory and analysed using diffraction data from X-ray crystallography. H-Ala-Gly-Ala-OH binds to the virus's surface by electrostatic interactions with the phosphate backbone of the nucleic acid, preventing it from infecting cells. At low temperatures, HAAGAO can inhibit both DNA and RNA synthesis in vitro, but at higher temperatures it only inhibits RNA synthesis.

Formula: C₈H₁₅N₃O₄

Purity: Min. 95%

Molecular weight: 217.22 g/mol

Ref: 3D-FA108458