23576-42-3 Usage
Description
PHE-GLY-GLY, also known as a tripeptide, is a sequence of three amino acids consisting of one L-phenylalanine and two glycine residues. This specific arrangement of amino acids provides unique properties and potential applications in various industries.
Uses
Used in Pharmaceutical Industry:
PHE-GLY-GLY is used as a building block for the development of new pharmaceutical compounds due to its unique structure and the ability to interact with other molecules. Its potential applications in drug design and development can be attributed to the specific arrangement of amino acids, which may allow for targeted interactions with biological targets.
Used in Cosmetic Industry:
PHE-GLY-GLY is used as an ingredient in cosmetic products for its potential moisturizing and skin-conditioning properties. The presence of glycine, a natural component of collagen, may contribute to the overall skin health and hydration when used in cosmetic formulations.
Used in Food Industry:
PHE-GLY-GLY can be used as a flavor enhancer or additive in the food industry. The presence of L-phenylalanine, an essential amino acid, may contribute to the overall taste and aroma of certain food products, making it a valuable component in the development of new flavors and taste profiles.
Used in Research and Development:
PHE-GLY-GLY serves as a valuable research tool for studying the properties and interactions of amino acids in various biological systems. Its unique structure allows scientists to investigate the role of specific amino acid sequences in protein folding, stability, and function, furthering our understanding of biological processes and potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 23576-42-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,5,7 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 23576-42:
(7*2)+(6*3)+(5*5)+(4*7)+(3*6)+(2*4)+(1*2)=113
113 % 10 = 3
So 23576-42-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H17N3O4/c14-10(6-9-4-2-1-3-5-9)13(20)16-7-11(17)15-8-12(18)19/h1-5,10H,6-8,14H2,(H,15,17)(H,16,20)(H,18,19)
23576-42-3Relevant articles and documents
N -boc deprotection and isolation method for water-soluble zwitterionic compounds
Liu, Zhijian,Yasuda, Nobuyoshi,Simeone, Michael,Reamer, Robert A.
, p. 11792 - 11796 (2015/02/19)
A highly efficient TMSI-mediated deprotection and direct isolation method to obtain zwitterionic compounds from the corresponding N-Boc derivatives has been developed. This method has been demonstrated in the final deprotection/isolation of the β-lactamase inhibitor MK-7655 as a part of its manufacturing process. Further application of this process toward other zwitterionic compounds, such as dipeptides and tripeptides, has been successfully developed. Furthermore, a catalytic version of this transformation has been demonstrated in the presence of BSA or BSTFA.
ATRIOPEPTINS. II. SYNTHESIS OF N-TERMINAL FRAGMENTS
Ovchinnikov, Mikhail V.,Bespalova, Zhanna D.,Molokoedov, Aleksandr S.,Revenko, Inna V.,Sepetov, Nikolai F.,et al
, p. 784 - 795 (2007/10/02)
Peptides, corresponding to the N-terminal sequence in atriopeptins, were synthesized by classical methods of peptide chemistry in solutions.The obtained peptides were characterized by various physicochemical methods.The scheme and methods of the synthesis are discussed.
