6803-19-6 Usage
Description
S-(P-NITROBENZYL)GLUTATHIONE is a glutathione derivative in which the thiol hydrogen of glutathione is replaced by a 4-nitrobenzyl group. It is a compound with potential applications in various industries due to its unique chemical properties.
Uses
Used in Pharmaceutical Industry:
S-(P-NITROBENZYL)GLUTATHIONE is used as a pharmaceutical agent for its potential therapeutic effects. It can be utilized in the development of drugs targeting specific diseases or conditions, given its unique structure and properties.
Used in Chemical Research:
In the field of chemical research, S-(P-NITROBENZYL)GLUTATHIONE serves as a valuable compound for studying the interactions between glutathione and other molecules. Its 4-nitrobenzyl group allows researchers to investigate the role of glutathione in various biological processes and its potential as a therapeutic agent.
Used in Analytical Chemistry:
S-(P-NITROBENZYL)GLUTATHIONE can be employed as a reagent or standard in analytical chemistry for the detection and quantification of glutathione or related compounds. Its distinct chemical properties make it suitable for use in assays and other analytical techniques.
Used in Biochemical Applications:
In biochemical applications, S-(P-NITROBENZYL)GLUTATHIONE can be used to study the role of glutathione in cellular processes, such as detoxification and redox regulation. Its modified structure allows for the investigation of the effects of glutathione modifications on its function and interactions with other biomolecules.
Overall, S-(P-NITROBENZYL)GLUTATHIONE is a versatile compound with potential applications in various industries, including pharmaceuticals, chemical research, analytical chemistry, and biochemical applications. Its unique structure and properties make it a valuable tool for studying glutathione's role in biological processes and its potential as a therapeutic agent.
Check Digit Verification of cas no
The CAS Registry Mumber 6803-19-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,0 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6803-19:
(6*6)+(5*8)+(4*0)+(3*3)+(2*1)+(1*9)=96
96 % 10 = 6
So 6803-19-6 is a valid CAS Registry Number.
InChI:InChI=1/C17H22N4O8S/c18-12(17(26)27)5-6-14(22)20-13(16(25)19-7-15(23)24)9-30-8-10-1-3-11(4-2-10)21(28)29/h1-4,12-13H,5-9,18H2,(H,19,25)(H,20,22)(H,23,24)(H,26,27)/t12-,13-/m0/s1
6803-19-6Relevant articles and documents
Efficient S-alkylation of cysteine in the presence of 1,1,3,3- tetramethylguanidine
W?ostowski, Marek,Czarnocka, Sylwia,MacIejewski, Piotr
, p. 5977 - 5979 (2010)
The synthesis of S-alkylated cysteine derivatives was carried out successfully in the presence of 1,1,3,3-tetramethylguanidine. Alkylation proceeded in high yields on unprotected amino acids and peptides containing a sulfhydryl group.
