Cyclo(-Asp-Gly) is a cyclic dipeptide composed of the amino acids aspartic acid (Asp) and glycine (Gly). This compound features a unique cyclic structure that can influence its biochemical properties and interactions. The cyclic nature of Cyclo(-Asp-Gly) can enhance its stability compared to linear peptides, potentially making it more resistant to enzymatic degradation. It exhibits characteristics typical of peptides, such as the ability to form hydrogen bonds and engage in various interactions with biological macromolecules. Cyclo(-Asp-Gly) may also play a role in biological processes, including signaling pathways and cellular functions, due to its structural conformation. Additionally, the presence of the aspartic acid residue introduces a negatively charged side chain at physiological pH, which can affect the compound's solubility and interaction with other molecules. Overall, Cyclo(-Asp-Gly) is of interest in biochemical research and potential therapeutic applications, particularly in the fields of drug design and development.

Cyclo(-Asp-Gly)

52661-97-9: Cyclo(-Asp-Gly) is a cyclic dipeptide composed of the amino acids aspartic acid (Asp) and glycine (Gly). This compound features a unique cyclic structure that can influence its biochemical properties and interactions. The cyclic nature of Cyclo(-Asp-Gly) can enhance its stability compared to linear peptides, potentially making it more resistant to enzymatic degradation. It exhibits characteristics typical of peptides, such as the ability to form hydrogen bonds and engage in various interactions with biological macromolecules. Cyclo(-Asp-Gly) may also play a role in biological processes, including signaling pathways and cellular functions, due to its structural conformation. Additionally, the presence of the aspartic acid residue introduces a negatively charged side chain at physiological pH, which can affect the compound's solubility and interaction with other molecules. Overall, Cyclo(-Asp-Gly) is of interest in biochemical research and potential therapeutic applications, particularly in the fields of drug design and development.

CAS 52661-97-9

Cyclo(-Asp-Gly)

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Ref: IN-DA00D8GH

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