38678-61-4

Usage

Uses

Used in Pharmaceutical Industry:
H-PHE-GLY-NH2 HCL is used as a building block for the synthesis of various pharmaceutical compounds due to its constituent amino acids, phenylalanine and glycine, which are essential for protein synthesis and neurotransmitter production.
Used in Nutraceutical Industry:
H-PHE-GLY-NH2 HCL is used as a dietary supplement to support protein synthesis and neurotransmitter production, promoting overall health and well-being.
Used in Cosmetic Industry:
H-PHE-GLY-NH2 HCL is used as an active ingredient in cosmetic products for its potential skin health benefits, such as promoting collagen synthesis and improving skin elasticity.
Used in Research Applications:
H-PHE-GLY-NH2 HCL is used as a research tool in biological and chemical studies to investigate the functions and interactions of amino acids, peptides, and neurotransmitters in various biological processes.

Upstream product

• 42726-70-5 Boc-Phe-Gly-NH₂ 
• 35661-40-6 N-Fmoc L-Phe 
• 1349173-17-6 Fmoc-Phe-Gly-NH₂ 
• 63-91-2 L-phenylalanine 
• 598-41-4 H-Gly-NH₂ 
• 3674-06-4 Boc-Phe-ONSu 
• 17187-05-2 Z-L-phenylalanylglycinamide 

Downstream Products

• 144923-43-3 Boc-L-Pyr(Bu^t)-D-Gly(OMe)-L-Phe-Gly-NH₂ 
• 144923-43-3 Boc-L-Tyr(Bu^t)-L-Gly(OMe)-L-Phe-Gly-NH₂ 
• 1349173-14-3 C₁₅H₂₀N₄O₃ 
• 1349173-18-7 C₃₄H₃₄N₄O₃ 
• 1402723-37-8 C₂₄H₂₇N₅O₄ 
• 165900-95-8 Z-Tyr(SO₃H)-D-Ala-Phe-Gly-NH₂ 
• 165900-94-7 Z-Tyr-D-Ala-Phe-Gly-NH₂ 

Relevant academic research and scientific papers

Aziridine-mediated ligation and site-specific modification of unprotected peptides

A synthesis of aziridine-containing peptides via the Cu(II)-promoted coupling of unprotected peptide thioacids and N-H aziridine-2-carbonyl peptides is reported. The unique reactivity of the resulting N-acylated aziridine-2-carbonyl peptides facilitates t

Ribozymomimetic chemical synthesis of peptide bond using phosphorous acid/oxirane mediators

Chemical Equation Presented A model system is created that mimics natural ribosome as well as the way of ribozyme action. It uses oxirane analogue as condensation reagent and H3PO3 as activator for the carboxyl group and as protecting reagent for the NH2

2,2-Dimethyl-2-(o-nitrophenyl)acetyl (DMNA) as an assisted cleavage protecting group for amines

2,2-Dimethyl-2-(o-nitrophenyl)acetyl group (DMNA) was explored as an assisted cleavage protecting group for amines and a one-step deprotection condition was developed for its efficient removal using hydrogenation in the presence of Pd-C or PtO2 catalyst and 10% HOAc in MeOH. DMNA was found to be especially useful for the synthesis of gem-diamino compounds using Hofmann rearrangement.

Synthesis and opioid activity of tyrosine sulfate containing dermorphin and deltorphin peptides

To study the effect of the sulfate ester moiety on the opioid activity, we prepared two tyrosine sulfate-(Tyr(SO3H))-containing dermorphin and deltorphin peptides. Their activities were determined in binding studies based on displacement of μ-