41036-33-3 Usage
Description
H-ALA-ALA-NH2 HCL is a dipeptide molecule composed of two alanine amino acids and a C-terminal amide group, with a hydrochloride salt. Alanine, being a nonpolar and hydrophobic amino acid, forms a neutral, uncharged molecule when combined in a dipeptide. H-ALA-ALA-NH2 HCL is frequently utilized in research and laboratory settings, serving as a building block for larger peptides or as a reference material in various tests and analyses. The hydrochloride salt form enhances its solubility in aqueous solutions, facilitating experimental procedures. H-ALA-ALA-NH2 HCL is a fundamental dipeptide with broad potential applications in the fields of biochemistry and biomedical research.
Uses
Used in Biochemical Research:
H-ALA-ALA-NH2 HCL is used as a building block for the synthesis of larger peptides, contributing to the development of novel bioactive compounds and therapeutic agents.
Used in Laboratory Testing and Analysis:
H-ALA-ALA-NH2 HCL is used as a reference material to ensure the accuracy and reliability of experimental procedures and analytical techniques in biochemical and biomedical research.
Used in Pharmaceutical Development:
H-ALA-ALA-NH2 HCL is used as a starting compound in the design and synthesis of new pharmaceuticals, potentially leading to the discovery of innovative treatments for various diseases and conditions.
Used in Biomedical Research:
H-ALA-ALA-NH2 HCL is employed in the study of peptide structure, function, and interactions, providing insights into the fundamental aspects of biochemistry and advancing our understanding of biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 41036-33-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,0,3 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 41036-33:
(7*4)+(6*1)+(5*0)+(4*3)+(3*6)+(2*3)+(1*3)=73
73 % 10 = 3
So 41036-33-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H13N3O2.ClH/c1-3(7)6(11)9-4(2)5(8)10;/h3-4H,7H2,1-2H3,(H2,8,10)(H,9,11);1H
41036-33-3Relevant articles and documents
Serine-Protease-Assisted Synthesis of Peptide Substrates for α-Chymotripsin
Bizzozero, Spartaco A.,Rovagnati, Bruno A.,Dutler, Hans
, p. 1707 - 1719 (1982)
δ-Chymotrypsin catalyzes peptide-bond formation between acylated amino-acid and peptide esters as the carboxyl component and amino-acid and peptide amides as the amino component.The conditions under which enzyme-catalyzed coupling can be used for fragment condensation in peptide synthesis is investigated.To illustrate the method the synthesis of tetra-, penta and hexapeptides of the structure Ac-Lxn-...-Lxl-Lyl-...-Lym-NH2 with Lxl = Tyr, designed as substrates for α-chymotrypsin is described.
