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Oxidized glutathione

Oxidized glutathione structure

Oxidized glutathione 

structure
  • CAS No:

    27025-41-8

  • Formula:

    C20H32N6O12S2

  • Chemical Name:

    Oxidized glutathione

  • Synonyms:

    Glycine,L-γ-glutamyl-L-cysteinyl-,bimol. (2→2′)-disulfide;Glutamine,N,N′-[dithiobis[1-[(carboxymethyl)carbamoyl]ethylene]]di-,L-;Glutamine,N,N′-[dithiobis[1-[(carboxymethyl)carbamoyl]ethylene]]di-;Glutathione-SSG;GSSG;Oxidized glutathione;Glutathione,disulfide;Glutathione,oxidized;Glutathione-S-S-glutathione;Oxidized L-glutathione;Glutathione disulphide;Sleep-promoting factor B;Oxiglutatione;Selenoglutathione;121-24-4;10421-65-5;87140-29-2;97908-42-4;371915-35-4;475558-84-0;1254121-37-3;1260488-58-1;2394733-76-5

  • Categories:

    Cosmetic Ingredient  >  Skin Conditioning

Description

Glutathione oxidized is produced by the oxidation of glutathione which is a major intracellular antioxidant and detoxifying agent.


Solid


Glutathione disulfide is an organic disulfide and a glutathione derivative. It has a role as an Escherichia coli metabolite and a mouse metabolite. It is a conjugate acid of a glutathione disulfide(2-).|A GLUTATHIONE dimer formed by a disulfide bond between the cysteine sulfhydryl side chains during the course of being oxidized.|Oxiglutatione is the oxidized disulfide form of glutathione (GSH) with potential protective activity. Glutathione disulfide (GSSG) is reduced by glutathione reductase to GSH. GSSG and GSH together play important roles in numerous redox reactions, such as those involved in the detoxification of harmful substances and free radicals, and in reactions preventing oxidative damage in erythrocytes. Upon ocular administration in irrigation solution, glutathione disulfide may exert a beneficial effect on the intracellular redox state of glutathione, thereby protecting the integrity and barrier function of the corneal endothelial cells.

Oxidized glutathione Basic Attributes

612.63

612.151978

248-170-7

ULW86O013H

DTXSID5048972

C62624

29309090

Characteristics

368

-9.1

Solid

1.7±0.1 g/cm3

170-172 °C

1196.5°C at 760 mmHg

544.3±37.1 °C

1.677

soluble

2-8ºC

0mmHg at 25°C

224.7 Ų [M+H]+ [CCS Type: DT, Method: single field calibrated with Agilent tune mix (Agilent)]|227 Ų [M+H]+ [CCS Type: TW, Method: calibrated with polyalanine]

Safety Information

NONH for all modes of transport

2

R36/37/38

S26-S36-S24/25

MC0556500

Xi: Irritant;

Stable. Incompatible with strong oxidizing agents.

P264, P280, P302+P352, P305+P351+P338, P321, P332+P313, P337+P313, P362

H315

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 8 companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

Disulfide, Glutathione

Oxidized glutathione Use and Manufacturing

Uses

L(-)-Glutathione is a biomarker for fatty liver disease. S,S'-Ethylenebis(glutathione) is a haloethane-glutathione conjugate formed via GSH transferases. S,S'-Ethylenebis(glutathione) formation is used to study the polymorphism in glutathione conjugation ac tivity of human erythrocytes towards ethylene dibromide.

Human Drugs -> FDA Approved Drug Products with Therapeutic Equivalence Evaluations (Orange Book) -> Active Ingredients

Computed Properties

Molecular Weight:612.6
XLogP3:-9.1
Hydrogen Bond Donor Count:10
Hydrogen Bond Acceptor Count:16
Rotatable Bond Count:21
Exact Mass:612.15196282
Monoisotopic Mass:612.15196282
Topological Polar Surface Area:368
Heavy Atom Count:40
Complexity:879
Defined Atom Stereocenter Count:4
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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