473452-81-2 Usage
Description
L-Proline, L-lysyl-5-oxo-, also known as Lysyl-proline or lysyl-5-oxo-L-proline, is a chemical compound derived from the amino acid proline. It plays a vital role in the formation of collagen, an essential protein for the structure and function of connective tissues in the body.
Uses
Used in Cosmetic and Skincare Industry:
L-Proline, L-lysyl-5-oxois used as an active ingredient in cosmetic and skincare products for its ability to support collagen synthesis and promote tissue regeneration. This helps in reducing the signs of skin aging, improving wound healing, and enhancing tissue repair.
Used in Pharmaceutical Industry:
L-Proline, L-lysyl-5-oxohas potential applications in the development of pharmaceuticals for treating conditions related to connective tissue disorders. Its role in collagen formation and tissue regeneration makes it a promising candidate for therapeutic interventions in such conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 473452-81-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,3,4,5 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 473452-81:
(8*4)+(7*7)+(6*3)+(5*4)+(4*5)+(3*2)+(2*8)+(1*1)=162
162 % 10 = 2
So 473452-81-2 is a valid CAS Registry Number.
473452-81-2Relevant articles and documents
Modelling of prebiotic synthesis and selection of peptides under isothermal conditions and thermal cycling mode
Demina,Kononikhin,Laptev,Khodonov,Nikolaev,Varfolomeev
, p. 422 - 441 (2013/06/27)
The model peptide synthesis from mixtures of amino acids was carried out under the thermal cycling and isothermal modes. The compositions of the obtained mixtures of products and the primary amino acid sequence of the synthesized peptides were determined by Fourier transform ion cyclotron resonance mass spectrometry and tandem mass spectrometry in combination with high-performance liquid chromatography with the application of de novo sequencing of the synthesized products. The processes of abiogenous synthesis of peptides were shown to occur under relatively mild temperature conditions and give a substantially less number of peptides as compared with the possible statistical set. The evolution of the system takes place in the process of the synthesis in solid phase with the disappearance of a series of the most unstable peptides. The selection process with the formation of complementary peptides takes place in peptide synthesis under the thermal cyclic mode.