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15483-27-9

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15483-27-9 Usage

Definition

ChEBI: A dipeptide formed from two L-arginine residues.

Check Digit Verification of cas no

The CAS Registry Mumber 15483-27-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,8 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 15483-27:
(7*1)+(6*5)+(5*4)+(4*8)+(3*3)+(2*2)+(1*7)=109
109 % 10 = 9
So 15483-27-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H26N8O3/c13-7(3-1-5-18-11(14)15)9(21)20-8(10(22)23)4-2-6-19-12(16)17/h7-8H,1-6,13H2,(H,20,21)(H,22,23)(H4,14,15,18)(H4,16,17,19)

15483-27-9SDS

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 (2S)-2-[[(2S)-2-amino-5-(diaminomethylideneamino)pentanoyl]amino]-5-(diaminomethylideneamino)pentanoic acid

1.2 Other means of identification

Product number -
Other names L-Arg-L-Arg

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:15483-27-9 SDS

15483-27-9Downstream Products

15483-27-9Relevant articles and documents

Ester-mediated peptide formation promoted by deep eutectic solvents: a facile pathway to proto-peptides

Chien, Chen-Yu,Yu, Sheng-Sheng

supporting information, p. 11949 - 11952 (2020/10/15)

The ester-amide exchange reaction enables spontaneous formation of prebiotic proto-peptides under mild conditions. However, this reaction also leads to oligomers with a vast sequence diversity of ester and amide linkages. Here, we demonstrate using deep eutectic solvents as a universal strategy to regulate the reaction pathways and promote the formation of amino acid-enriched oligomers with peptide backbones.

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.

Compositions and Methods for Binding Lysophosphatidic Acid

-

, (2009/06/27)

Compositions and methods for making and using anti-LPA agents, for example, monoclonal antibodies, are described.

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