10329-75-6 Usage
Description
LEU-LEU-LEU, also known as a tripeptide formed from three L-leucine residues, is a white powder with unique chemical properties. It is derived from the amino acid L-leucine, which is one of the essential branched-chain amino acids (BCAAs) that play a crucial role in various biological processes.
Uses
Used in Pharmaceutical Industry:
LEU-LEU-LEU is used as a pharmaceutical compound for its potential therapeutic applications. The tripeptide structure allows it to interact with specific receptors and proteins, making it a promising candidate for the development of new drugs targeting various diseases.
Used in Nutritional Supplements:
In the sports nutrition and health supplement industry, LEU-LEU-LEU is used as an ingredient to support muscle growth and recovery. Its role as a BCAA contributes to the maintenance of muscle mass and provides energy during exercise, making it a popular choice for athletes and fitness enthusiasts.
Used in Research and Development:
LEU-LEU-LEU is utilized as a research tool in the field of biochemistry and molecular biology. Its unique structure and properties make it an interesting subject for studying protein-protein interactions, peptide synthesis, and other related processes.
Used in Cosmetics Industry:
In the cosmetics industry, LEU-LEU-LEU is used as an active ingredient in skincare and hair care products. Its potential benefits include promoting skin regeneration, improving skin elasticity, and providing antioxidant protection, making it a valuable addition to various cosmetic formulations.
Check Digit Verification of cas no
The CAS Registry Mumber 10329-75-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,2 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10329-75:
(7*1)+(6*0)+(5*3)+(4*2)+(3*9)+(2*7)+(1*5)=76
76 % 10 = 6
So 10329-75-6 is a valid CAS Registry Number.
InChI:InChI=1/C18H35N3O4/c1-10(2)7-13(19)16(22)20-14(8-11(3)4)17(23)21-15(18(24)25)9-12(5)6/h10-15H,7-9,19H2,1-6H3,(H,20,22)(H,21,23)(H,24,25)
10329-75-6Relevant articles and documents
A novel L-amino acid ligase from bacillus subtilis NBRC3134 catalyzed oligopeptide synthesis
Kino, Kuniki,Arai, Toshinobu,Tateiwa, Daisuke
experimental part, p. 129 - 134 (2010/04/24)
L-Amino acid ligase catalyzes dipeptide synthesis from unprotected L-amino acids in an ATP-dependent manner. We have purified a new L-amino acid ligase, RizA, which synthesizes dipeptides whose N-terminus is Arg, from Bacillus subtilis NBRC3134, a microorganism that produces a rhizocticin peptide antibiotic. It was suggested that RizA is probably involved in rhizocticin biosynthesis. In this study, we performed sequence analysis of unknown regions around rizA, and newly identified a gene that encodes a protein that possesses an ATP-grasp motif upstream of rizA. This gene was designated rizB, and its recombinant protein was prepared. Recombinant RizB synthesized homo-oligo-mers of branched-chain L-amino acids and L-methionine consisting of two to five amino acids in an ATP-dependent manner. RizB also synthesized various heteropeptides. Further examination showed that RizB might elongate a peptide chain at the N-terminus. This is the first report on an L-amino acid ligase catalyzing oligopeptide synthesis.
