65163-25-9 Usage
General Description
L-alanine (3-13C) is a stable, non-radioactive isotope of the amino acid L-alanine that contains a carbon-13 atom at the third position of the molecule. L-alanine is a non-essential amino acid that is important for protein synthesis, and it plays a role in the glucose-alanine cycle, where it helps to transport carbon and nitrogen between tissues. The incorporation of the carbon-13 isotope into L-alanine allows for the tracking of metabolic pathways and the study of biochemical processes using techniques like nuclear magnetic resonance (NMR) spectroscopy. This labeled form of L-alanine can be used in research and pharmaceutical development for studying metabolism, protein synthesis, and other biochemical processes in living organisms.
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 articles and documents
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
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
