24787-87-9 Usage
Description
Z-SER-ALA-OH is a small molecule chemical compound composed of three amino acids: serine, alanine, and a carboxylic acid group. Serine, a non-essential amino acid, plays a crucial role in protein synthesis and neurotransmitter production, while alanine, an essential amino acid, is involved in energy production and blood sugar regulation. The carboxylic acid group, a functional group in many organic compounds, is vital for peptide bond formation in proteins. Z-SER-ALA-OH may have potential applications in pharmaceuticals, biochemistry, and molecular biology due to its unique structure and properties.
Uses
Used in Pharmaceutical Industry:
Z-SER-ALA-OH is used as a building block for the development of peptide-based drugs, leveraging its amino acid composition and carboxylic acid group to facilitate peptide bond formation and enhance drug efficacy.
Used in Biochemistry Research:
Z-SER-ALA-OH serves as a valuable tool in biochemical research, enabling scientists to study protein synthesis, peptide bond formation, and the role of specific amino acids in various biological processes.
Used in Molecular Biology Applications:
In molecular biology, Z-SER-ALA-OH is utilized as a component in the design of novel bioactive peptides, exploring its potential to modulate biological functions and develop new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 24787-87-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,7,8 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 24787-87:
(7*2)+(6*4)+(5*7)+(4*8)+(3*7)+(2*8)+(1*7)=149
149 % 10 = 9
So 24787-87-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H18N2O6/c1-9(13(19)20)15-12(18)11(7-17)16-14(21)22-8-10-5-3-2-4-6-10/h2-6,9,11,17H,7-8H2,1H3,(H,15,18)(H,16,21)(H,19,20)
24787-87-9Relevant articles and documents
Selective Enzymatic Removal of Protecting Groups: n-Heptyl Esters as Carboxy Protecting Functions in Peptide Synthesis
Braun, Peter,Waldmann, Herbert,Vogt, Walter,Kunz, Horst
, p. 165 - 170 (2007/10/02)
Amino acid heptyl (Hep) esters are accessible as generally crystalline hydro tosylates 3 from the amino acids by azeotropic esterification with 1-heptanol in high yields.They can be condensed with Z-, Boc-, and Aloc-protected amino acids to give the dipep
