39692-63-2 Usage
Uses
Used in Pharmaceutical Development:
Z-DEHYDRO-ALA-OH is used as a building block for the synthesis of novel bioactive molecules and pharmaceuticals. Its unique properties allow for the creation of compounds with specific biological activities, contributing to the advancement of drug discovery and therapeutic interventions.
Used in Peptide and Protein Engineering:
Z-DEHYDRO-ALA-OH is utilized as a key component in the design and synthesis of peptides and proteins with tailored properties. Its incorporation into these biomolecules can modulate their stability, activity, and interactions with other biological systems, facilitating the development of new therapeutic agents and diagnostic tools.
Used in Chemical Biology Research:
Z-DEHYDRO-ALA-OH serves as a valuable probe in chemical biology, enabling researchers to study the role of dehydroalanine residues in various biological processes. Its unique reactivity and structural features make it an ideal candidate for investigating protein function, protein-protein interactions, and the mechanisms of post-translational modifications.
Used in the Study of Protein Structure and Function:
Z-DEHYDRO-ALA-OH is employed as a tool to explore the structural and functional aspects of proteins containing dehydroalanine residues. Its presence in proteins can lead to the formation of novel covalent bonds and structural motifs, providing insights into protein folding, stability, and function.
Check Digit Verification of cas no
The CAS Registry Mumber 39692-63-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,6,9 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 39692-63:
(7*3)+(6*9)+(5*6)+(4*9)+(3*2)+(2*6)+(1*3)=162
162 % 10 = 2
So 39692-63-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H11NO4/c1-8(10(13)14)12-11(15)16-7-9-5-3-2-4-6-9/h2-6H,1,7H2,(H,12,15)(H,13,14)
39692-63-2Relevant academic research and scientific papers
Synthesis of nucleo aminooxy acid derivatives
Noel, Olivier,Xie, Juan
, p. 134 - 140 (2013/03/13)
Nucleobase-functionalized peptides have attracted increasing interest because of their well-ordered secondary structures and stability toward enzymatic degradations. We have designed and synthesized nucleo aminooxy acids as novel building blocks for nucle
A Useful and Biomimetic Synthesis of N-Acyl α,β-Dehydroalanine form Aspartic Acid
Seki, Masahiko,Moriya, Tamon,Matsumoto, Kazuo
, p. 1251 - 1256 (2007/10/02)
N-Acyl α,β-dehydroalanines (1) were synthesized from the corresponding N-acyl aspartic acids by a one-pot procedure through a biomimetic oxidative β-decarboxylation.In particular, the transformation using methanol-sodium hypochlorite aqueous solution, which served for N-chlorination and dehydrochlorination, afforded good yields of (1).
Synthesis of β-lactam antibiotics by the sulfeno-cycloamination
Ihara,Haga,Yonekura,et al.
, p. 7345 - 7352 (2007/10/02)
A novel efficient beta -lactam synthesis was achieved by two successive processes (sulfeno-cycloamination), addition of phenysulfenyl chloride to alpha , beta -unsaturated amides followed by base treatment. Key synthetic intermediates of monobactams and nocardicin derivatives were obtained via this method. construction of the 1-carbapenam ring system by the sulfenocycloamination is also described.
