863-16-1

Basic information

• Product Name: N-(N²-benzyloxycarbonyl-L-glutaminyl)-L-tyrosine
• CAS NO: 863-16-1
• Molecular Weight: 443.456
• Mol File: 863-16-1.mol
• Article Data: 0

Chemical Properties

• CAS DataBase Reference: N-(N²-benzyloxycarbonyl-L-glutaminyl)-L-tyrosine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(N²-benzyloxycarbonyl-L-glutaminyl)-L-tyrosine(863-16-1)
• EPA Substance Registry System: N-(N²-benzyloxycarbonyl-L-glutaminyl)-L-tyrosine(863-16-1)

Safety Data

• Hazardous Substances Data: 863-16-1(Hazardous Substances Data)

Usage

Description

N-(N2-benzyloxycarbonyl-L-glutaminyl)-L-tyrosine is a synthetic peptide composed of L-glutaminyl and L-tyrosine amino acids. It is utilized in biochemical research and drug development as a model compound for investigating the metabolism and transport of peptides within the body. The N2-benzyloxycarbonyl group serves as a chemical protective group that temporarily masks the reactive amine group of the glutamine amino acid, enabling specific peptide modification without affecting its overall structure. This synthetic peptide holds potential therapeutic applications due to its capacity to target specific receptors or enzymes in the body.

Uses

Used in Biochemical Research:
N-(N2-benzyloxycarbonyl-L-glutaminyl)-L-tyrosine is used as a model compound for studying the metabolism and transport of peptides in the body. Its application aids in understanding the fundamental processes and mechanisms involved in peptide interactions and functions.
Used in Drug Development:
In the pharmaceutical industry, N-(N2-benzyloxycarbonyl-L-glutaminyl)-L-tyrosine is used as a compound for developing new drugs. Its ability to target specific receptors or enzymes makes it a promising candidate for therapeutic applications, potentially leading to the creation of novel treatments for various diseases and conditions.
Used in Chemical Protective Group Applications:
The N2-benzyloxycarbonyl group in N-(N2-benzyloxycarbonyl-L-glutaminyl)-L-tyrosine is used as a chemical protective group in the synthesis of peptides. It temporarily masks the reactive amine group of the glutamine amino acid, allowing for specific modifications to the peptide without altering its overall structure. This application is crucial in the development of peptides with desired properties and functions.

Upstream product

• 13907-82-9 N²-benzyloxycarbonyl-L-glutamine methyl ester 
• 4008-03-1 N²-benzyloxycarbonyl-L-glutamine hydrazide