65163-25-9 Usage
Uses
Used in Research and Pharmaceutical Development:
L-ALANINE (3-13C) is used as a research tool for studying metabolism, protein synthesis, and other biochemical processes in living organisms. The incorporation of the carbon-13 isotope allows for the precise tracking and analysis of these processes, providing valuable insights into the underlying mechanisms and potential therapeutic targets.
Used in Metabolic Pathway Analysis:
L-ALANINE (3-13C) is used as a tracer in metabolic pathway analysis to identify and quantify the flow of carbon and nitrogen through various biochemical reactions. This information is essential for understanding the regulation of metabolic processes and the development of targeted therapies for metabolic disorders.
Used in Biochemical Process Investigation:
L-ALANINE (3-13C) is used as a probe in the investigation of biochemical processes, such as enzyme kinetics and substrate specificity. The labeled form of L-alanine allows researchers to monitor the interactions between enzymes and their substrates, providing insights into the mechanisms of enzymatic reactions and the design of enzyme inhibitors or activators.
Used in NMR Spectroscopy:
L-ALANINE (3-13C) is used as a labeled compound in nuclear magnetic resonance (NMR) spectroscopy to study the structure and dynamics of proteins and other biomolecules. The carbon-13 isotope provides a unique signature in NMR spectra, enabling the identification and characterization of specific amino acid residues and their interactions within the molecular structure.
Used in Tissue Engineering and Regenerative Medicine:
L-ALANINE (3-13C) is used as a component in tissue engineering and regenerative medicine applications to promote cell growth and tissue repair. The amino acid plays a crucial role in protein synthesis and collagen production, which are essential for the formation and maintenance of extracellular matrices and the regeneration of damaged tissues.
Used in Nutritional Studies:
L-ALANINE (3-13C) is used as a labeled compound in nutritional studies to investigate the metabolism and utilization of amino acids in the human body. The incorporation of the carbon-13 isotope allows researchers to track the absorption, distribution, and excretion of L-alanine, providing insights into the nutritional requirements and metabolic pathways of this essential amino acid.
Check Digit Verification of cas no
The CAS Registry Mumber 65163-25-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,1,6 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 65163-25:
(7*6)+(6*5)+(5*1)+(4*6)+(3*3)+(2*2)+(1*5)=119
119 % 10 = 9
So 65163-25-9 is a valid CAS Registry Number.
65163-25-9Relevant academic research and scientific papers
The metabolic and biochemical impact of glucose 6-sulfonate (sulfoquinovose), a dietary sugar, on carbohydrate metabolism
Sacoman, Juliana L.,Badish, Lauren N.,Sharkey, Thomas D.,Hollingsworth, Rawle I.
, p. 21 - 29,9 (2012/12/12)
Increased activity of the main carbohydrate pathways (glycolysis, pentose phosphate, and hexosamine biosynthetic pathways) is one of the hallmarks of metabolic diseases such as cancer. Sulfoquinovosyl diacylglycerol is a sulfoglycolipid found in the human
The metabolic and biochemical impact of glucose 6-sulfonate (sulfoquinovose), a dietary sugar, on carbohydrate metabolism
Sacoman, Juliana L.,Badish, Lauren N.,Sharkey, Thomas D.,Hollingsworth, Rawle I.
, p. 21 - 29 (2013/01/15)
Increased activity of the main carbohydrate pathways (glycolysis, pentose phosphate, and hexosamine biosynthetic pathways) is one of the hallmarks of metabolic diseases such as cancer. Sulfoquinovosyl diacylglycerol is a sulfoglycolipid found in the human
An asymmetric synthesis of L-[3-13C]alanine
Takatori, Kazuhiko,Toyama, Sanae,Narumi, Shoko,Fujii, Seishiro,Kajiwara, Masahiro
, p. 91 - 94 (2007/10/03)
L-[3-13C]Alanine was synthesized from [13C]methyl iodide by using Dellaria's oxazinone, prepared from phenyl[2- 13C]bromoacetate and (S)-2-phenylglycinol, as a chiral glycine equivalent. Alkylation of the oxazinone with [13C]methyl iodide was achieved with high diastereoselectivity. Hydrolysis and removal of the chiral auxiliary of the alkylated oxazinone gave L-[3-13C]alanine. Copyright
