Z-.beta.-Ala-Gly-Gly-OH, also known as Z-beta-alanylglycylglycine, is a synthetic peptide characterized by its specific amino acid sequence. The "Z" indicates the presence of a protective group, typically benzyloxycarbonyl (Z), which is commonly used in peptide synthesis to protect the amino group of the first amino acid. The structure consists of beta-alanine followed by two glycine residues, making it a tripeptide. This compound is often utilized in biochemical research and pharmaceutical applications due to its potential role in modulating biological processes. Its properties include solubility in polar solvents, stability under physiological conditions, and the ability to interact with various biological targets. The CAS number 102601-37-6 uniquely identifies this compound in chemical databases, facilitating its study and application in various fields, including medicinal chemistry and peptide synthesis. As with many peptides, its biological activity can be influenced by factors such as concentration, environment, and the presence of other molecules.

Z-.beta.-Ala-Gly-Gly-OH

102601-37-6: Z-.beta.-Ala-Gly-Gly-OH, also known as Z-beta-alanylglycylglycine, is a synthetic peptide characterized by its specific amino acid sequence. The "Z" indicates the presence of a protective group, typically benzyloxycarbonyl (Z), which is commonly used in peptide synthesis to protect the amino group of the first amino acid. The structure consists of beta-alanine followed by two glycine residues, making it a tripeptide. This compound is often utilized in biochemical research and pharmaceutical applications due to its potential role in modulating biological processes. Its properties include solubility in polar solvents, stability under physiological conditions, and the ability to interact with various biological targets. The CAS number 102601-37-6 uniquely identifies this compound in chemical databases, facilitating its study and application in various fields, including medicinal chemistry and peptide synthesis. As with many peptides, its biological activity can be influenced by factors such as concentration, environment, and the presence of other molecules.

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CAS 102601-37-6

Z-.beta.-Ala-Gly-Gly-OH

Z-β-Ala-Gly-Gly-OH

Ref: 3D-FA111438