3918-87-4 Usage
Description
H-PHE-ALA-OH, also known as L-phenylalanyl-L-alanine, is a dipeptide formed from L-phenylalanine and L-alanine residues. It is a white powder with unique chemical properties that make it suitable for various applications across different industries.
Uses
Used in Pharmaceutical Industry:
H-PHE-ALA-OH is used as an active pharmaceutical ingredient for its potential therapeutic effects. The dipeptide structure allows it to interact with specific receptors or enzymes in the body, making it a promising candidate for the development of new drugs targeting various health conditions.
Used in Cosmetic Industry:
In the cosmetic industry, H-PHE-ALA-OH is used as a key ingredient in skincare and beauty products due to its potential benefits for the skin. The dipeptide may help improve skin elasticity, reduce the appearance of fine lines and wrinkles, and promote a more youthful and radiant complexion.
Used in Food and Beverage Industry:
H-PHE-ALA-OH is used as a flavor enhancer and additive in the food and beverage industry. The dipeptide can contribute to the overall taste and aroma of various products, making them more appealing to consumers.
Used in Research and Development:
H-PHE-ALA-OH is also utilized in research and development for its potential applications in biotechnology and pharmaceuticals. Scientists and researchers can use this dipeptide to study its interactions with biological systems and develop new therapies or products based on these findings.
Check Digit Verification of cas no
The CAS Registry Mumber 3918-87-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,1 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3918-87:
(6*3)+(5*9)+(4*1)+(3*8)+(2*8)+(1*7)=114
114 % 10 = 4
So 3918-87-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H16N2O3/c1-8(12(16)17)14-11(15)10(13)7-9-5-3-2-4-6-9/h2-6,8,10H,7,13H2,1H3,(H,14,15)(H,16,17)/t8-,10-/m0/s1
3918-87-4Relevant articles and documents
A dynamic combinatorial library for biomimetic recognition of dipeptides in water
Klepel, Florian,Ravoo, Bart Jan
supporting information, p. 1588 - 1595 (2020/09/16)
Small peptides are involved in countless biological processes. Hence selective binding motifs for peptides can be powerful tools for labeling or inhibition. Finding those binding motifs, especially in water which competes for intermolecular H-bonds, poses an enormous challenge. A dynamic combinatorial library can be a powerful method to overcome this issue. We previously reported artificial receptors emerging form a dynamic combinatorial library of peptide building blocks. In this study we aimed to broaden this scope towards recognition of small peptides. Employing CXC peptide building blocks, we found that cyclic dimers of oxidized CFC bind to the aromatic peptides FF and YY (K ≈ 229-702 M-1), while AA binds significantly weaker (K ≈ 65-71 M-1).
Branched peptide linkers
-
, (2008/06/13)
Conjugates containing a targeting ligand, such as an antibody, a therapeutically active drug and a branched peptide linker. The branched peptide linker contains two or more amino acid moieties that provide an enzyme cleavage site. The number of drugs capable of being bonded to the branched linkers varies by a factor of two for each generation of branching.
Selective deprotection of phthalyl protected amines
Costello, Colleen A.,Kreuzman, Adam J.,Zmijewski, Milton J.
, p. 7469 - 7472 (2007/10/03)
Phthalyl amidase selectively deprotects phthalimido groups under very mild aqueous conditions in a one-pot reaction to produce phthalic acid and the free amine. The enzyme has been shown to deprotect several primary amines of distinctly different structure, and exhibits chiral selectivity when the substrate contains extensive β-branching. The enzyme has a definite requirement for ortho positioning of the functional groups on a fixed axis of rotation.
