H-Pro-His-Val-OH, also known as a peptide with the sequence of proline (Pro), histidine (His), and valine (Val), is a small molecule that exhibits characteristics typical of peptides. It is a part of a class of compounds known as amino acid derivatives, which play crucial roles in biological processes. This substance is likely to be soluble in water due to the presence of polar amino acids, particularly histidine, which can participate in hydrogen bonding. The presence of proline, known for its unique cyclic structure, can impart rigidity to the peptide chain, influencing its conformation and biological activity. H-Pro-His-Val-OH may exhibit biological activity, potentially acting as a signaling molecule or influencing metabolic pathways. Its CAS number, 83960-33-2, allows for precise identification in chemical databases. As with many peptides, stability can be affected by factors such as pH and temperature, and it may be subject to enzymatic degradation in biological systems. Overall, H-Pro-His-Val-OH represents a fascinating example of the complexity and functionality of peptide-based compounds in biochemistry.

H-Pro-His-Val-OH

83960-33-2: H-Pro-His-Val-OH, also known as a peptide with the sequence of proline (Pro), histidine (His), and valine (Val), is a small molecule that exhibits characteristics typical of peptides. It is a part of a class of compounds known as amino acid derivatives, which play crucial roles in biological processes. This substance is likely to be soluble in water due to the presence of polar amino acids, particularly histidine, which can participate in hydrogen bonding. The presence of proline, known for its unique cyclic structure, can impart rigidity to the peptide chain, influencing its conformation and biological activity. H-Pro-His-Val-OH may exhibit biological activity, potentially acting as a signaling molecule or influencing metabolic pathways. Its CAS number, 83960-33-2, allows for precise identification in chemical databases. As with many peptides, stability can be affected by factors such as pH and temperature, and it may be subject to enzymatic degradation in biological systems. Overall, H-Pro-His-Val-OH represents a fascinating example of the complexity and functionality of peptide-based compounds in biochemistry.

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CAS 83960-33-2

H-Pro-His-Val-OH

H-Pro-His-Val-OH

Ref: IN-DA00G3JN

H-Pro-His-Val-OH

Ref: 3D-FP109354