The chemical substance known as "3-(4-AZIDOPHENYL)PROPIONYL-D-TYR(ME)-PHE-GLN-ASN-ARG-PRO-ARG-TYR-NH2" is a peptide derivative characterized by its unique structure, which includes an azide functional group attached to a phenyl ring, contributing to its potential applications in bioconjugation and click chemistry. The presence of the D-Tyrosine (D-TYR) and other amino acids such as Phenylalanine (PHE), Glutamine (GLN), Asparagine (ASN), Arginine (ARG), and Proline (PRO) indicates that it is a modified peptide, which may exhibit specific biological activities or interactions. The azide group is particularly noteworthy for its reactivity, allowing for selective coupling with alkyne-containing molecules, making it valuable in the fields of medicinal chemistry and biochemistry for labeling and tracking biomolecules. The peptide's sequence suggests potential roles in signaling or therapeutic applications, although specific biological properties would depend on its conformation and interactions within a biological system. Overall, this compound exemplifies the intersection of organic chemistry and peptide design, with implications for research and development in drug discovery and molecular biology.

3-(4-AZIDOPHENYL)PROPIONYL-D-TYR(ME)-PHE-GLN-ASN-ARG-PRO-ARG-TYR-NH2

157702-46-0: The chemical substance known as "3-(4-AZIDOPHENYL)PROPIONYL-D-TYR(ME)-PHE-GLN-ASN-ARG-PRO-ARG-TYR-NH2" is a peptide derivative characterized by its unique structure, which includes an azide functional group attached to a phenyl ring, contributing to its potential applications in bioconjugation and click chemistry. The presence of the D-Tyrosine (D-TYR) and other amino acids such as Phenylalanine (PHE), Glutamine (GLN), Asparagine (ASN), Arginine (ARG), and Proline (PRO) indicates that it is a modified peptide, which may exhibit specific biological activities or interactions. The azide group is particularly noteworthy for its reactivity, allowing for selective coupling with alkyne-containing molecules, making it valuable in the fields of medicinal chemistry and biochemistry for labeling and tracking biomolecules. The peptide's sequence suggests potential roles in signaling or therapeutic applications, although specific biological properties would depend on its conformation and interactions within a biological system. Overall, this compound exemplifies the intersection of organic chemistry and peptide design, with implications for research and development in drug discovery and molecular biology.

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CAS 157702-46-0

3-(4-AZIDOPHENYL)PROPIONYL-D-TYR(ME)-PHE-GLN-ASN-ARG-PRO-ARG-TYR-NH2

(3-(4-Azidophenyl)propionyl1,D-Tyr(Me)2,Arg6,Arg8,Tyr-NH29)-Vasopressin trifluoroacetate salt

Ref: 3D-FA109005