Z-Ala-Pro-Tyr-OH, also known as Z-Acetyl-L-alanylleucyl-L-tyrosine, is a synthetic peptide characterized by its sequence of amino acids: Z (benzyloxycarbonyl) protecting group, alanine (Ala), proline (Pro), and tyrosine (Tyr), followed by a carboxylic acid group (OH). This compound is typically utilized in biochemical research and pharmaceutical applications due to its structural properties that can influence biological activity. The Z protecting group enhances the stability and solubility of the peptide, making it suitable for various synthetic and analytical processes. The presence of proline contributes to the peptide's conformational rigidity, while tyrosine, with its aromatic side chain, can participate in interactions such as hydrogen bonding and π-π stacking, which are crucial for protein folding and function. Additionally, the compound's CAS number, 112898-29-0, allows for precise identification in chemical databases. Overall, Z-Ala-Pro-Tyr-OH serves as a valuable tool in peptide synthesis and studies related to protein interactions and functions.

Z-Ala-Pro-Tyr-OH

112898-29-0: Z-Ala-Pro-Tyr-OH, also known as Z-Acetyl-L-alanylleucyl-L-tyrosine, is a synthetic peptide characterized by its sequence of amino acids: Z (benzyloxycarbonyl) protecting group, alanine (Ala), proline (Pro), and tyrosine (Tyr), followed by a carboxylic acid group (OH). This compound is typically utilized in biochemical research and pharmaceutical applications due to its structural properties that can influence biological activity. The Z protecting group enhances the stability and solubility of the peptide, making it suitable for various synthetic and analytical processes. The presence of proline contributes to the peptide's conformational rigidity, while tyrosine, with its aromatic side chain, can participate in interactions such as hydrogen bonding and π-π stacking, which are crucial for protein folding and function. Additionally, the compound's CAS number, 112898-29-0, allows for precise identification in chemical databases. Overall, Z-Ala-Pro-Tyr-OH serves as a valuable tool in peptide synthesis and studies related to protein interactions and functions.

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CAS 112898-29-0

Z-Ala-Pro-Tyr-OH

Z-Ala-Pro-Tyr-OH

Ref: 3D-FA111445