615-82-7 Usage
Uses
Used in Biochemical Research:
DL-Leucyl-Glycine is used as a biochemical reagent for its role in protein synthesis and as a substrate for various enzymes involved in metabolism. It aids in understanding the fundamental processes of biological systems.
Used in Pharmaceutical Production:
In the pharmaceutical industry, DL-Leucyl-Glycine is utilized in the production of drugs, leveraging its properties to enhance the efficacy and function of certain medications.
Used in Medical Research:
DL-Leucyl-Glycine is studied for its potential therapeutic effects in conditions such as cancer and metabolic disorders, making it a valuable compound in the search for new treatments and therapies.
Used in Cosmetics Industry:
Although not explicitly mentioned in the provided materials, DL-Leucyl-Glycine, given its biochemical properties, could potentially be used in the cosmetics industry for its role in protein synthesis and enzyme activity, which may contribute to skin health and rejuvenation.
Check Digit Verification of cas no
The CAS Registry Mumber 615-82-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 615-82:
(5*6)+(4*1)+(3*5)+(2*8)+(1*2)=67
67 % 10 = 7
So 615-82-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H16N2O3/c1-5(2)3-6(9)8(13)10-4-7(11)12/h5-6H,3-4,9H2,1-2H3,(H,10,13)(H,11,12)/t6-/m0/s1
615-82-7Relevant academic research and scientific papers
Peptide Synthesis Using the Pyrrole Ring as an Amino Protecting Group
Kashima, Choji,Maruyama, Tatsuya,Harada, Kazuo,Hibi, Shigeki,Omote, Yoshimori
, p. 601 - 645 (2007/10/02)
The utility of a pyrrole ring as an amino protecting group for amino acids in peptide synthesis has been studied.The N-termini of various amino acids (1) were protected with a pyrrole ring by treatment with 2,5-dimethoxytetrahydrofuran (10) to give 2-substituted 2-(1-pyrrolyl)acetic acids (11).The peptide bond between (11) and amino acid methyl ester (2) was formed using N,N'-dicyclohexylcarbodiimide, and the pyrrole ring was cleaved by ozonolysis and hydrolysis without the cleavage of a peptide bond to give the corresponding dipeptide compounds (26) in good yields.
Peptide Decomposition in the Neutral pH Region via the Formation of Diketopiperazines
Steinberg, Spencer M.,Bada, Jeffrey L.
, p. 2295 - 2298 (2007/10/02)
In the neutral pH region, the decomposition of the tripeptides Leu-Gly-Gly and Gly-Leu-Gly at 130 deg C and the hexapeptide Phe-Gly-Leu-Gly-Val-Gly at 100 deg C has been found to involve the formation of diketopiperazines from the N-terminal position of the peptides.
