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H-ASP-LYS-OH, also known as L-aspartic acid-L-lysine, is a dipeptide consisting of two amino acids: L-aspartic acid and L-lysine. In H-ASP-LYS-OH, the carboxyl group of aspartic acid forms a peptide bond with the amino group of lysine, resulting in a molecule with the structure H-ASP-LYS-OH. This dipeptide plays a crucial role in various biological processes, including protein synthesis and cell signaling. It is also used in pharmaceuticals, cosmetics, and food industries due to its potential health benefits and properties.

5891-51-0

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5891-51-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5891-51-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,9 and 1 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5891-51:
(6*5)+(5*8)+(4*9)+(3*1)+(2*5)+(1*1)=120
120 % 10 = 0
So 5891-51-0 is a valid CAS Registry Number.

5891-51-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name H-Asp-Lys-OH

1.2 Other means of identification

Product number -
Other names L-aspartyl-lysine acetate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5891-51-0 SDS

5891-51-0Relevant academic research and scientific papers

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.

Synthesis and activity of NAcSerAspLysPro analogues on cellular interactions between T-cell and erythrocytes in rosette formation

Thierry,Papet,Saez-Servent,Plissonneau-Haumont,Potier,Lenfant

, p. 2122 - 2127 (2007/10/02)

Analogues of NAcSerAspLysPro (AcSDKP), a natural regulator of hematopoiesis isolated from fetal calf bone marrow, were synthesized. The biological activity of these molecules were evaluated in vitro in the rosette assay, which measures the interaction bet

The Relationship between Taste and Primary Structure of "Delicious Peptide" (Lys-Gly-Asp-Glu-Glu-Ser-Leu-Ala) from Beef Soup

Tamura, Masahiro,Nakatsuka, Tohru,Tada, Makoto,Kawasaki, Yoshihiro,Kikuchi, Eiichi,Okai, Hideo

, p. 319 - 326 (2007/10/02)

"Delicious peptide" was reported to be as delicious as beef soup.The peptide and its fragments were synthesized to study its taste active sites. "Delicious peptide" was found to produce a umami and a sour taste.By preparing several di- or tripeptides composed of basic or acidic amino acids, we found that the taste of "delicious peptide" was produced by an interaction between the basic and the acidic fragments in the peptide.

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