Welcome to LookChem.com Sign In|Join Free
  • or
H-ARG-GLU-OH is a chemical compound composed of three amino acids: arginine (ARG), glutamic acid (GLU), and a hydroxyl group (OH). Arginine, an essential amino acid, is vital for protein synthesis, immune function, and blood pressure regulation. Glutamic acid, a non-essential amino acid, acts as a neurotransmitter in the central nervous system and contributes to sugar and fat metabolism. The hydroxyl group, consisting of an oxygen and hydrogen atom, is a common functional group in organic compounds. This unique combination of amino acids and functional groups in H-ARG-GLU-OH may possess diverse biological and chemical properties.

15706-89-5

Post Buying Request

15706-89-5 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

15706-89-5 Usage

Uses

Used in Pharmaceutical Industry:
H-ARG-GLU-OH is used as a pharmaceutical compound for its potential therapeutic effects. The presence of arginine and glutamic acid may contribute to the regulation of various physiological processes, such as immune response and neurotransmission.
Used in Nutraceutical Industry:
H-ARG-GLU-OH is used as a nutraceutical ingredient for its potential health benefits. The combination of amino acids may support protein synthesis, cognitive function, and overall well-being.
Used in Cosmetic Industry:
H-ARG-GLU-OH is used as an active ingredient in cosmetic products for its potential skin benefits. The amino acids and hydroxyl group may contribute to skin hydration, elasticity, and overall skin health.
Used in Research and Development:
H-ARG-GLU-OH is used as a research compound for studying the interactions between amino acids and functional groups in various biological and chemical processes. This knowledge can lead to the development of new therapeutic agents and applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 15706-89-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,7,0 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 15706-89:
(7*1)+(6*5)+(5*7)+(4*0)+(3*6)+(2*8)+(1*9)=115
115 % 10 = 5
So 15706-89-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H21N5O5/c12-6(2-1-5-15-11(13)14)9(19)16-7(10(20)21)3-4-8(17)18/h6-7H,1-5,12H2,(H,16,19)(H,17,18)(H,20,21)(H4,13,14,15)

15706-89-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[[2-amino-5-(diaminomethylideneamino)pentanoyl]amino]pentanedioic acid

1.2 Other means of identification

Product number -
Other names arginyl glutamic acid

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:15706-89-5 SDS

15706-89-5Downstream Products

15706-89-5Relevant 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.

A novel L-amino acid ligase from Bacillus subtilis NBRC3134, a microorganism producing peptide-antibiotic rhizocticin

Kino, Kuniki,Kotanaka, Yoichi,Arai, Toshinobu,Yagasaki, Makoto

body text, p. 901 - 907 (2009/11/30)

L-Amino acid ligase catalyzes the formation of an α-peptide bond from unprotected L-amino acids in an ATP-dependent manner, and this enzyme is very useful in efficient peptide production. We performed enzyme purification to obtain a novel L-amino acid lig

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 15706-89-5