Ac-Gly-Arg-Gly-NH2, also known as Acetyl-Glycine-Arginine-Glycine-Amide, is a synthetic peptide that features a sequence of amino acids including glycine, arginine, and an amide group. This compound is characterized by its acetylation at the N-terminus, which enhances its stability and bioavailability. The presence of the arginine residue contributes to its potential biological activity, particularly in cell signaling and interactions with various receptors. The amide group at the C-terminus can influence the peptide's solubility and reactivity. Ac-Gly-Arg-Gly-NH2 is often studied in the context of drug development, particularly for its roles in cellular processes such as angiogenesis and wound healing. Its structural properties allow it to mimic natural peptides, making it a valuable tool in biochemical research and therapeutic applications. As with many peptides, its stability can be affected by environmental factors such as pH and temperature, which are important considerations in its handling and storage.

Ac-Gly-Arg-Gly-NH2

176520-14-2: Ac-Gly-Arg-Gly-NH2, also known as Acetyl-Glycine-Arginine-Glycine-Amide, is a synthetic peptide that features a sequence of amino acids including glycine, arginine, and an amide group. This compound is characterized by its acetylation at the N-terminus, which enhances its stability and bioavailability. The presence of the arginine residue contributes to its potential biological activity, particularly in cell signaling and interactions with various receptors. The amide group at the C-terminus can influence the peptide's solubility and reactivity. Ac-Gly-Arg-Gly-NH2 is often studied in the context of drug development, particularly for its roles in cellular processes such as angiogenesis and wound healing. Its structural properties allow it to mimic natural peptides, making it a valuable tool in biochemical research and therapeutic applications. As with many peptides, its stability can be affected by environmental factors such as pH and temperature, which are important considerations in its handling and storage.

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CAS 176520-14-2

Ac-Gly-Arg-Gly-NH2

Ac-Gly-Arg-Gly-NH2

Ref: 3D-FA110259