63546-27-0 Usage
Description
L-ALANINE-3,3,3-D3 is a labeled analogue of L-Alanine, a non-essential amino acid for human development and one of the 20 amino acids encoded by the genetic code. L-ALANINE-3,3,3-D3 is utilized in various scientific and medical applications due to its unique properties and ability to provide insights into metabolic processes.
Uses
Used in Medical Research:
L-ALANINE-3,3,3-D3 is used as a tracer compound for in-vivo measurement of glucose and alanine metabolism, particularly in studies involving patients with diabetes. The use of this labeled analogue allows researchers to track and analyze metabolic pathways and better understand the impact of diabetes on these processes.
Used in Pharmaceutical Development:
As a labeled amino acid, L-ALANINE-3,3,3-D3 can be employed in the development of pharmaceuticals targeting metabolic disorders. Its ability to provide insights into the metabolic pathways involving alanine and glucose can aid in the design of more effective treatments and therapies for conditions such as diabetes.
Used in Nutritional Studies:
L-ALANINE-3,3,3-D3 can be utilized in nutritional studies to investigate the role of L-Alanine in human development and health. By tracking the labeled compound, researchers can gain a better understanding of the amino acid's absorption, metabolism, and overall contribution to the body's nutritional needs.
Check Digit Verification of cas no
The CAS Registry Mumber 63546-27-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,5,4 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 63546-27:
(7*6)+(6*3)+(5*5)+(4*4)+(3*6)+(2*2)+(1*7)=130
130 % 10 = 0
So 63546-27-0 is a valid CAS Registry Number.
63546-27-0Relevant articles and documents
RATIONAL SYNTHESIS OF DEUTERIUM-LABELLED PYRIDOXAL AND PYRIDOXAL ALKALOIDS
Bringmann, Gerhard,Schneider, Stephan
, p. 175 - 178 (2007/10/02)
A synthesis of pyridoxal is described, which avoids delicate redox reactions at the accomplished pyridoxyl system.This synthesis allows the facile preparation of highly (>98percent) deuterated pyridoxal 10b and of B6-derived alkaloids.