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Glycine, L-a-glutamylglycyl-, also known as glutathione, is a tripeptide composed of three amino acids: glycine, L-glutamic acid, and L-cysteine. It plays a crucial role in various biological processes, including antioxidant defense, detoxification, and immune system regulation. As a powerful antioxidant, glutathione helps protect cells from oxidative stress and damage caused by free radicals. It also plays a vital role in the detoxification process by binding to harmful substances and facilitating their elimination from the body. Additionally, glutathione is involved in the regulation of the immune system, supporting the body's natural defense mechanisms against infections and diseases. Overall, glycine, L-a-glutamylglycyl- (glutathione) is an essential component in maintaining cellular health and function.

6706-20-3

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6706-20-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6706-20-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,0 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6706-20:
(6*6)+(5*7)+(4*0)+(3*6)+(2*2)+(1*0)=93
93 % 10 = 3
So 6706-20-3 is a valid CAS Registry Number.

6706-20-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name L-α-glutamyl=>glycyl=>glycine

1.2 Other means of identification

Product number -
Other names L-α-Glutamyl=>glycyl=>glycin

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:6706-20-3 SDS

6706-20-3Downstream Products

6706-20-3Relevant academic research and scientific papers

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.

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