1195967-46-4 Usage
Uses
Used in Fitness and Bodybuilding Industry:
Leucic acid is used as a dietary supplement for its potential to promote muscle protein synthesis and muscle growth. It is particularly favored in the fitness and bodybuilding industry due to its ability to support muscle development and strength gains.
Used in Sports Nutrition:
As an anti-catabolic agent, Leucic acid is used to help prevent muscle breakdown and improve recovery after exercise. This makes it a valuable component in sports nutrition products designed to support athletes and fitness enthusiasts in their training and performance goals.
Used in Health and Wellness Applications:
Leucic acid is used as a nutritional supplement for its potential role in improving insulin sensitivity and fat metabolism. This makes it appealing to individuals looking to optimize their body composition and overall health by supporting a healthy metabolism and insulin function.
Used in Pharmaceutical Industry:
Given its potential health benefits, Leucic acid may also be utilized in the development of pharmaceutical products aimed at addressing muscle wasting conditions, improving athletic performance, and enhancing metabolic health.
Check Digit Verification of cas no
The CAS Registry Mumber 1195967-46-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,5,9,6 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1195967-46:
(9*1)+(8*1)+(7*9)+(6*5)+(5*9)+(4*6)+(3*7)+(2*4)+(1*6)=214
214 % 10 = 4
So 1195967-46-4 is a valid CAS Registry Number.
1195967-46-4Relevant articles and documents
Robust asymmetric synthesis of unnatural alkenyl amino acids for conformationally constrained α-helix peptides
Aillard, Boris,Robertson, Naomi S.,Baldwin, Adam R.,Robins, Siobhan,Jamieson, Andrew G.
supporting information, p. 8775 - 8782 (2014/12/11)
The efficient asymmetric synthesis of unnatural alkenyl amino acids required for peptide 'stapling' has been achieved using alkylation of a fluorine-modified NiII Schiff base complex as the key step.
