473452-81-2 Usage
General Description
L-Proline, L-lysyl-5-oxo- is a chemical compound that is a derivative of the amino acid proline. It is also known as Lysyl-proline or lysyl-5-oxo-L-proline. L-Proline, L-lysyl-5-oxo- plays a crucial role in the formation of collagen, which is an essential protein for the structure and function of connective tissues in the body. Additionally, L-Proline, L-lysyl-5-oxo- has been used in studies related to skin aging, wound healing, and tissue repair. Its ability to support collagen synthesis and promote tissue regeneration makes it a valuable component in cosmetic and skincare products. Furthermore, it has potential applications in the development of pharmaceuticals for treating conditions related to connective tissue disorders.
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.
