63623-57-4 Usage
Uses
Used in Pharmaceutical and Biotechnology Industry:
Z-GLY-NVA-OH is used as a building block for the synthesis of peptides and larger molecules, facilitating the development of new drugs and therapeutic agents. Its ability to mimic natural peptides makes it instrumental in drug discovery and research, contributing to the advancement of pharmaceutical formulations and treatments.
Used in Drug Discovery:
Z-GLY-NVA-OH is used as a structural mimic for natural peptides, aiding in the identification and development of novel therapeutic agents. Its role in mimicking natural peptide structures is crucial for understanding their functions and interactions within biological systems, thereby enhancing the discovery of new drugs and treatments.
Used in Antimicrobial Applications:
Z-GLY-NVA-OH is used as an antimicrobial agent for its potential to inhibit the growth of certain bacteria and fungi. Its effectiveness in this area is significant for the development of new antimicrobial therapies and treatments, particularly in the face of increasing antibiotic resistance.
Used in Organic Chemistry Research:
Z-GLY-NVA-OH is used as a research tool in organic chemistry, enabling scientists to explore the synthesis and properties of peptides and larger molecules. Its versatility in this field is essential for advancing the understanding of peptide chemistry and its applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 63623-57-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,6,2 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 63623-57:
(7*6)+(6*3)+(5*6)+(4*2)+(3*3)+(2*5)+(1*7)=124
124 % 10 = 4
So 63623-57-4 is a valid CAS Registry Number.
InChI:InChI=1/C15H20N2O5/c1-2-6-12(14(19)20)17-13(18)9-16-15(21)22-10-11-7-4-3-5-8-11/h3-5,7-8,12H,2,6,9-10H2,1H3,(H,16,21)(H,17,18)(H,19,20)
63623-57-4Relevant academic research and scientific papers
PEPTIDE BOND FORMATION UNDER PHASE-TRANSFER CONDITIONS. EFFECT OF AMINO ACID STRUCTURE
Kosmynin, V. V.,Kaida, L. N.,Savelova, V. A.,Taran, N. A.
, p. 2306 - 2311 (2007/10/02)
The extraction of amino acids NH2CH(R)COOH in the two-phase system consisting of 1-butanol and an amino acid buffer solution in the presence of cetyltrimethylammonium bromide and also the kinetics of the aminolysis of N-benzyloxycarbonylglycine p-nitrophe
