4368-66-5 Usage
Uses
Used in Pharmaceutical Development:
L-Leucine, N-(N-glycyl-L-phenylalanyl)-, methyl ester is used as a potential drug candidate for its enhanced bioavailability and pharmacokinetic properties, which may contribute to the development of novel therapeutic agents.
Used in Biochemical Research:
In the field of biochemistry, L-Leucine, N-(N-glycyl-L-phenylalanyl)-, methyl ester is used as a research tool to study protein synthesis and metabolism, aiding in the understanding of these processes and their implications in various biological systems.
Used in Nutritional Supplements:
Given its role in protein synthesis and muscle growth, L-Leucine, N-(N-glycyl-L-phenylalanyl)-, methyl ester may be utilized in the development of nutritional supplements to support athletic performance and muscle recovery.
Used in Cosmetics Industry:
L-Leucine, N-(N-glycyl-L-phenylalanyl)-, methyl ester's potential for improved bioavailability and pharmacokinetic properties could also make it a valuable ingredient in cosmetic products, particularly those targeting skin health and regeneration.
Used in Agricultural Applications:
L-Leucine, N-(N-glycyl-L-phenylalanyl)-, methyl ester may have applications in agriculture, particularly in the development of biostimulants and growth promoters for crops, due to its role in protein synthesis and metabolism.
Check Digit Verification of cas no
The CAS Registry Mumber 4368-66-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,6 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4368-66:
(6*4)+(5*3)+(4*6)+(3*8)+(2*6)+(1*6)=105
105 % 10 = 5
So 4368-66-5 is a valid CAS Registry Number.
4368-66-5Relevant academic research and scientific papers
AMIDE BOND ISOSTERES: IMIDAZOLINES IN PSEUDOPEPTIDE CHEMISTRY
Jones, Raymond C.F.,Ward, Gary J.
, p. 3853 - 3856 (2007/10/02)
The 2-imidazole ring has been incorporated as an amide bond replacement into pseudodipeptides, a pseudotripeptide, and pseudopentapeptide enkephalin analogues.
Synthesis and Conformations of Stereochemically Restricted Analogs of Leu5-Enkephalinamide: Substitution of α-Aminoisobutyric Acid and 1-Aminocyclopentane-1-carboxylic Acid at Positions 2 and 3
Kishore, R.,Balaram, P.
, p. 1137 - 1144 (2007/10/02)
Six analogs of Leu-enkephalinamide containing α-aminoisobutyric acid (Aib) or 1-amino-cyclopentane-1-carboxylic acid (Acc5) at positions 2 and 3 have been synthesized.The peptides Tyr-Aib-Gly-Phe-Leu-NH2 (1), Tyr-Gly-Aib-Phe-Leu-NH2 (2), Tyr-Ai
