Z-D-Homophe-OH, identified by its CAS number 138812-70-1, is a chemical compound that belongs to the class of peptides or peptide analogs. It is characterized by its specific structural features, which include a modified amino acid sequence that may influence its biological activity and interactions. Typically, compounds like Z-D-Homophe-OH are utilized in research settings, particularly in studies related to peptide synthesis, drug development, and biochemical assays. The "Z" in its name often indicates the presence of a protective group, which is commonly used in peptide chemistry to prevent unwanted reactions during synthesis. The hydroxyl (-OH) group suggests potential for hydrogen bonding, which can affect solubility and reactivity. Overall, Z-D-Homophe-OH is of interest in medicinal chemistry and pharmacology, where understanding its properties can lead to insights into its function and potential therapeutic applications. However, specific details regarding its physical properties, reactivity, and applications would require further investigation or access to specialized databases.

Z-D-Homophe-OH

138812-70-1: Z-D-Homophe-OH, identified by its CAS number 138812-70-1, is a chemical compound that belongs to the class of peptides or peptide analogs. It is characterized by its specific structural features, which include a modified amino acid sequence that may influence its biological activity and interactions. Typically, compounds like Z-D-Homophe-OH are utilized in research settings, particularly in studies related to peptide synthesis, drug development, and biochemical assays. The "Z" in its name often indicates the presence of a protective group, which is commonly used in peptide chemistry to prevent unwanted reactions during synthesis. The hydroxyl (-OH) group suggests potential for hydrogen bonding, which can affect solubility and reactivity. Overall, Z-D-Homophe-OH is of interest in medicinal chemistry and pharmacology, where understanding its properties can lead to insights into its function and potential therapeutic applications. However, specific details regarding its physical properties, reactivity, and applications would require further investigation or access to specialized databases.

Z-D-Homophe-oh

<p>(R)-2-(((Benzyloxy)carbonyl)amino)-4-phenylbutanoic acid</p>

CAS 138812-70-1

Z-D-Homophe-OH

Z-D-Homophe-oh

Ref: IN-DA0019NC

(R)-2-(((Benzyloxy)carbonyl)amino)-4-phenylbutanoic acid

Ref: 54-OR1065185

(R)-2-(((Benzyloxy)carbonyl)amino)-4-phenylbutanoic acid

Ref: 10-F222387