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N-oxalylcysteine is a chemical compound derived from the amino acid cysteine through its reaction with oxalyl chloride. It is characterized by the presence of a carboxylic acid group and a thiol group, which endow it with unique chemical properties. N-oxalylcysteine has garnered interest due to its potential protective role against oxidative stress and inflammation, exhibiting antioxidant and cytoprotective properties. Its therapeutic potential spans various diseases and conditions linked to oxidative damage, and it is also considered for its utility as a chelating agent for heavy metal ions and as a precursor in the synthesis of other biologically active compounds.

106984-15-0

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106984-15-0 Usage

Uses

Used in Pharmaceutical Industry:
N-oxalylcysteine is used as a therapeutic agent for its potential role in mitigating oxidative stress and inflammation. Its antioxidant and cytoprotective properties make it a candidate for the treatment of diseases and conditions associated with oxidative damage.
Used in Environmental Applications:
N-oxalylcysteine is utilized as a chelating agent for heavy metal ions, which can be crucial in environmental remediation processes to mitigate the toxic effects of heavy metals in ecosystems.
Used in Chemical Synthesis:
In the field of chemical synthesis, N-oxalylcysteine serves as a precursor for the production of other biologically active compounds, contributing to the development of new pharmaceuticals and other bioactive substances.

Check Digit Verification of cas no

The CAS Registry Mumber 106984-15-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,9,8 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 106984-15:
(8*1)+(7*0)+(6*6)+(5*9)+(4*8)+(3*4)+(2*1)+(1*5)=140
140 % 10 = 0
So 106984-15-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H7NO5S/c7-3(5(10)11)6-2(1-12)4(8)9/h2,12H,1H2,(H,6,7)(H,8,9)(H,10,11)/t2-/m0/s1

106984-15-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-2-(oxaloamino)-3-sulfanylpropanoic acid

1.2 Other means of identification

Product number -
Other names N-Oxalylcysteine

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:106984-15-0 SDS

106984-15-0Downstream Products

106984-15-0Related news

Oxalyl thiolesters and N-oxalylcysteine (cas 106984-15-0) are normal mammalian metabolites08/08/2019

SummaryA method for the quantitative analysis of N-oxalylcysteine and oxalyl thiolesters (RSCOCOO−) in biological samples is described. These compounds were found in all rat tissues examined (kidney, liver, brain, heart, muscle and fat), with the amount of N-oxalylcysteine ranging up to 18 nmole...detailed

Determination of oxalyl thiolesters, N-oxalylcysteine (cas 106984-15-0) and N-oxalylcysteamine in biological materials08/07/2019

A convenient method is described for the quantitative analysis of oxalyl thiolesters (OTEs), a newly discovered class of mammalian metabolites, in biological samples. By this particular technique the total concentration of all OTEs in the sample is determined. The method involves first reacting ...detailed

106984-15-0Relevant academic research and scientific papers

Dynamic combinatorial mass spectrometry leads to inhibitors of a 2-oxoglutarate-dependent nucleic acid demethylase

Woon, Esther C. Y.,Demetriades, Marina,Bagg, Eleanor A. L.,Aik, Weishen,Krylova, Svetlana M.,Ma, Jerome H. Y.,Chan, Munchiang,Walport, Louise J.,Wegman, David W.,Dack, Kevin N.,McDonough, Michael A.,Krylov, Sergey N.,Schofield, Christopher J.

supporting information; experimental part, p. 2173 - 2184 (2012/05/20)

2-Oxoglutarate-dependent nucleic acid demethylases are of biological interest because of their roles in nucleic acid repair and modification. Although some of these enzymes are linked to physiology, their regulatory roles are unclear. Hence, there is a de

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