H-Gly-Phe-Gly-OH, also known as Glycyl-Phenylalanylglycine, is a dipeptide composed of the amino acids glycine and phenylalanine. It features a glycine residue at both the N-terminus and C-terminus, with phenylalanine in the middle. This structure contributes to its unique properties, including its solubility in water and potential for forming hydrogen bonds due to the presence of amine and carboxylic acid functional groups. The peptide exhibits characteristics typical of peptides, such as the ability to participate in various biochemical reactions and interactions, making it relevant in fields like biochemistry and pharmacology. Its CAS number, 14656-09-8, allows for precise identification in chemical databases. H-Gly-Phe-Gly-OH may also play a role in biological processes, potentially influencing protein synthesis and cellular signaling pathways. Additionally, its stability and reactivity can be influenced by environmental factors such as pH and temperature, which are important considerations in both laboratory and industrial applications.

H-Gly-Phe-Gly-OH

14656-09-8: Glycyl-L-Phenylalanyl-Glycine, Glycylphenylalanylglycine, {[N-(ammonioacetyl)-L-phenylalanyl]amino}acetate

Gly-Phe-Gly-OH is a reactive, amide group containing molecule. It has an anionic nature, which means it will interact with peroxide and form a mononuclear complex. Gly-Phe-Gly-OH is also capable of reacting with cisplatin to form a tetradentate complex in the presence of two equivalents of tripeptides. The magnetic resonance spectroscopy study on this compound showed that it possesses a chromophore. This chromophore causes the molecule to rotate dihedrally and ligand to form hydrogen bonds in order to stabilize the molecule.

Gly-Phe-Gly-OH

GFG and GYG were used as model peptides in a study on the nitration of proteins.

CAS 14656-09-8: H-Gly-Phe-Gly-OH

Gly-Phe-Gly-OH

Ref: 3D-FG49316

H-Gly-Phe-Gly-OH

Ref: 01-4000624

Gly-Phe-Gly-OH

Ref: 10-F493116

Glycine, glycyl-L-phenylalanyl-

Ref: IN-DA001E58