S-(P-NITROBENZYL)GLUTATHIONE

S-(P-NITROBENZYL)GLUTATHIONE Suppliers list

Company Name:	Amadis Chemical Company Limited
Tel:	571-89925085
Email:	sales@amadischem.com
Products Intro:	Product Name:(2R)-2-[[(2S)-2-[[2-[[(2S,3R,4R,5S,6R)-3-acetamido-2,5-dihydroxy-6-(hydroxymethyl)-4-oxanyl]oxy]-1-oxopropyl]amino]-3-methyl-1-oxobutyl]amino]-5-amino-5-oxopentanoic acid CAS:6803-19-6 Purity:0.97 Package:mgs,gs,kgs Remarks:A835983

Company Name:	TargetMol Chemicals Inc.
Tel:	15002134094
Email:	marketing@targetmol.cn
Products Intro:	Product Name:S-(p-Nitrobenzyl)glutathione CAS:6803-19-6 Package:50mg;5mg

S-(P-NITROBENZYL)GLUTATHIONE Basic information

Product Name:	S-(P-NITROBENZYL)GLUTATHIONE
Synonyms:	S-(P-NITROBENZYL)GLUTATHIONE;s-(4-nitrobenzyl)glutathione;(2R)-2-[[(2S)-2-[[2-[[(2S,3R,4R,5S,6R)-3-acetamido-2,5-dihydroxy-6-(hydroxymethyl)-4-oxanyl]oxy]-1-oxopropyl]amino]-3-methyl-1-oxobutyl]amino]-5-amino-5-oxopentanoic acid;Glycine, L-γ-glutamyl-S-[(4-nitrophenyl)methyl]-L-cysteinyl-
CAS:	6803-19-6
MF:	C17H22N4O8S
MW:	442.44
EINECS:
Product Categories:	Glutathione and Derivatives;Dipeptides and Tripeptides;Peptides
Mol File:	6803-19-6.mol

S-(P-NITROBENZYL)GLUTATHIONE Chemical Properties

storage temp.

2-8°C

Safety Information

WGK Germany

MSDS Information

Provider	Language
SigmaAldrich	English

S-(P-NITROBENZYL)GLUTATHIONE Usage And Synthesis

Uses	S-(p-Nitrobenzyl)glutathione is a competitive glutathionase inhibitor. S-(p-Nitrobenzyl)glutathione is converted to the corresponding cysteine derivatives by rat kidney microsomes. S-(p-Nitrobenzyl)glutathione can be used for the research of metabolic breakdown of glutathione by the glutathionase system[1][2].
Definition	ChEBI: A glutathione derivative in which the thiol hydrogen of glutathione is replaced by a 4-nitrobenzyl group.
References	[1] I García-Sáez, et al. Molecular structure at 1.8 A of mouse liver class pi glutathione S-transferase complexed with S-(p-nitrobenzyl)glutathione and other inhibitors. J Mol Biol. 1994 Apr 1;237(3):298-314. DOI:10.1006/jmbi.1994.1232 [2] T Suga, et al. Studies on mercapturic acids. Participation of glutathionase in the conversion of glutathione derivatives to cysteine derivatives. J Biochem. 1966 Aug;60(2):133-9. DOI:10.1093/oxfordjournals.jbchem.a128411

S-(P-NITROBENZYL)GLUTATHIONE Preparation Products And Raw materials

Tag:S-(P-NITROBENZYL)GLUTATHIONE(6803-19-6) Related Product Information

L-Glutathione S-(4-nitrobenzyl)glutathione-iodo-4-azidosalicyclic acid 4-nitrobenzyl mercaptan H-CYS(BZL)-GLY-OH GSSG S-ETHYLGLUTATHIONE S-METHYLGLUTATHIONE H-GAMMA-GLU-GLY-GLY-OH 2-amino-4-(propan-2-ylcarbamoyl)butanoic acid S-(P-NITROBENZYL)GLUTATHIONE

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