81466-41-3 Usage
Uses
Used in Biochemical Research:
H-SER-ASN-OH is used as a research compound for studying the roles and interactions of serine and asparagine in various biological processes. This helps scientists to better understand the functions of these amino acids and their potential applications in medicine.
Used in Pharmaceutical Research:
H-SER-ASN-OH is used as a building block in the development of new pharmaceutical agents. Its unique combination of serine and asparagine may contribute to the creation of innovative drugs with specific therapeutic properties.
Used in the Development of Therapeutic Agents:
H-SER-ASN-OH is used as a component in the formulation of therapeutic agents targeting various diseases and conditions. The presence of serine and asparagine may provide specific benefits, such as enhancing protein synthesis or modulating cellular processes.
Used in the Development of Diagnostic Agents:
H-SER-ASN-OH is used as a component in the development of diagnostic agents that can help in the detection, monitoring, or assessment of certain diseases or conditions. H-SER-ASN-OH's unique properties may contribute to the sensitivity or specificity of these diagnostic tools.
Check Digit Verification of cas no
The CAS Registry Mumber 81466-41-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,4,6 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 81466-41:
(7*8)+(6*1)+(5*4)+(4*6)+(3*6)+(2*4)+(1*1)=133
133 % 10 = 3
So 81466-41-3 is a valid CAS Registry Number.
81466-41-3Relevant academic research and scientific papers
Peptides and method for synthesizing the same
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, (2008/06/13)
Disclosed herein are the peptides possibly radio-labelled and having primary structures represented by the general formula (I): wherein (1) X is H-Tyr-Gln-Ala-Lys and Y is a hydroxyl group, (2) X is pGlu-Ala-Lys(Nε -Tyr-H) and Y is a hydroxyl group, or (3) X is pGlu-Ala-Lys and Y is Tyr-OH. These peptides can be synthesized by bonding a pre-determined amino acid or a peptide to the nitrogen at one of the two ends of the starting material, H-Asn-OH or H-Asn-Tyr-OH, while leaving the carboxyl group at the other end thereof in a free state, and by successively repeating the same procedure on the thus prepared peptides. The symbols, Ser, Gln, Gly, Asn, Tyr, Ala and Lys used herein represent respectively a divalent residue formed by removing one hydrogen atom from the amino group of and further removing one hydroxyl group from the carboxyl group of the respective alpha- amino acids, serine, glutamine, glycine, asparagine, tyrosine, alanine and lysine. For instance, Ser represents the divalent residue, --NH--CH(CH2 OH)--CO--. The symbol, pGlu, represents a monovalent residue formed by removing one hydroxyl group from the carboxyl group of pyroglutamic acid.
