61348-28-5 Usage
Description
Boc-D-Glutamine, also known as N2-Boc-D-glutamine, is an N-Boc-protected form of D-Glutamine. D-Glutamine is an unnatural isomer of L-Glutamine, which is present in human plasma and serves as a source of liberated ammonia. It can be synthesized through enzymatic methods or found in various fermented products such as cheeses, wine, and vinegars. Boc-D-Glutamine is a white solid and is utilized in various applications across different industries.
Uses
Used in Pharmaceutical Industry:
Boc-D-Glutamine is used as an intermediate in the synthesis of various pharmaceutical compounds for [application reason]. Its N-Boc protection allows for selective deprotection and functionalization, making it a valuable building block in the development of new drugs.
Used in Biochemical Research:
In the field of biochemical research, Boc-D-Glutamine is used as a research tool for studying the role of D-Glutamine in biological processes and its interactions with enzymes and other biomolecules. This helps in understanding the mechanisms of various diseases and potential therapeutic targets.
Used in Enzyme Synthesis:
Boc-D-Glutamine is used as a substrate in the synthesis of enzymes that specifically utilize D-Glutamine, allowing researchers to study the enzyme's activity and optimize its production for industrial or medical applications.
Used in Food Industry:
In the food industry, Boc-D-Glutamine can be used as an additive to enhance the flavor and texture of certain products, as D-Glutamine is known to be present in fermented foods like cheese, wine, and vinegars.
Used in Cosmetics Industry:
Boc-D-Glutamine may also find applications in the cosmetics industry, where it can be used as an ingredient in skincare products due to its potential benefits for skin health and its role in cellular metabolism.
Check Digit Verification of cas no
The CAS Registry Mumber 61348-28-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,3,4 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 61348-28:
(7*6)+(6*1)+(5*3)+(4*4)+(3*8)+(2*2)+(1*8)=115
115 % 10 = 5
So 61348-28-5 is a valid CAS Registry Number.
61348-28-5Relevant articles and documents
Cγ(S/ R)-Bimodal Peptide Nucleic Acids (Cγ- bm-PNA) Form Coupled Double Duplexes by Synchronous Binding to Two Complementary DNA Strands
Bhingardeve, Pramod,Madhanagopal, Bharath Raj,Ganesh, Krishna N.
, p. 13680 - 13693 (2020/12/15)
Peptide nucleic acids (PNAs) are linear equivalents of DNA with a neutral acyclic polyamide backbone that has nucleobases attached via tert-amide link on repeating units of aminoethylglycine. They bind complementary DNA or RNA with sequence specificity to form hybrids that are more stable than the corresponding DNA/RNA self-duplexes. A new type of PNA termed bimodal PNA [Cγ(S/R)-bm-PNA] is designed to have a second nucleobase attached via amide spacer to a side chain at Cγon the repeating aeg units of PNA oligomer. Cγ-bimodal PNA oligomers that have two nucleobases per aeg unit are demonstrated to concurrently bind two different complementary DNAs, to form duplexes from both tert-amide side and Cγside. In such PNA:DNA ternary complexes, the two duplexes share a common PNA backbone. The ternary DNA 1:Cγ(S/R)-bm-PNA:DNA 2 complexes exhibit better thermal stability than the isolated duplexes, and the Cγ(S)-bm-PNA duplexes are more stable than Cγ(R)-bm-PNA duplexes. Bimodal PNAs are first examples of PNA analogues that can form DNA2:PNA:DNA1 double duplexes via recognition through natural bases. The conjoined duplexes of Cγ-bimodal PNAs can be used to generate novel higher-level assemblies.
