PHR1359

L-Glutathion réduit

Pharmaceutical Secondary Standard; Certified Reference Material

• Synonyme(s) : γ-L-Glutamyl-L-cystéinyl-glycine, GSH
• Formule linéaire : H₂NCH(CO₂H)CH₂CH₂CONHCH(CH₂SH)CONHCH₂CO₂H
• Numéro CAS: 70-18-8
• Poids moléculaire : 307.32
• Numéro Beilstein : 1729812
• Numéro CE : 200-725-4
• Numéro MDL: MFCD00065939
• Code UNSPSC : 41116107
• ID de substance PubChem : 329823339
• Nomenclature NACRES : NA.24

Propriétés

• Qualité: certified reference material; pharmaceutical secondary standard
• Niveau de qualité: 300
• Agence: traceable to Ph. Eur. Y0000517; traceable to USP 1294820
• Famille d'API: glutathione
• CofA (certificat d'analyse): current certificate can be downloaded
• Technique(s): HPLC: suitable; gas chromatography (GC): suitable
• Pf: 192-195 °C (dec.) (lit.)
• Application(s): pharmaceutical (small molecule)
• Format: neat
• Température de stockage: 2-30°C
• Chaîne SMILES: N[C@@H](CCC(=O)N[C@@H](CS)C(=O)NCC(O)=O)C(O)=O
• InChI: 1S/C10H17N3O6S/c11-5(10(18)19)1-2-7(14)13-6(4-20)9(17)12-3-8(15)16/h5-6,20H,1-4,11H2,(H,12,17)(H,13,14)(H,15,16)(H,18,19)/t5-,6-/m0/s1
• Clé InChI: RWSXRVCMGQZWBV-WDSKDSINSA-N

Description

Amino Acid Sequence

γ-Glu-Cys-Gly

Description générale

Glutathione (GSH) is the most important nonprotein thiol widely distributed in animal tissues, plants, and microorganisms. GSH is also a key determinant of redox signaling and protection against oxidative stress.
Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.

Application

These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements.

Peut être utilisé à 5-10 mM pour éluer la glutathion S-transférase (GST) à partir d′agarose-glutathion.

Actions biochimiques/physiologiques

Il s′agit d′un antioxydant endogène qui joue un rôle essentiel dans la réduction des espèces réactives de l′oxygène formées au cours du métabolisme cellulaire et de l′activation métabolique respiratoire. La glutathion S-transférase catalyse la formation de thioéthers de glutathion avec les xénobiotiques, les leucotriènes et d′autres molécules portant un centre électrophile. Le glutathion forme également des ponts disulfure avec les résidus cystéine des protéines. Via ces mécanismes, il peut avoir l′effet paradoxal de réduire l′efficacité des agents anticancéreux.

Remarque sur l'analyse

These secondary standards offer multi-traceability to the USP, EP (PhEur) and BP primary standards, where they are available.

Autres remarques

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Note de bas de page

To see an example of a Certificate of Analysis for this material enter LRAA7940 in the slot below. This is an example certificate only and may not be the lot that you receive.

Produits recommandés

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Informations sur la sécurité

• Code de la classe de stockage: 11 - Combustible Solids
• Classe de danger pour l'eau (WGK): WGK 2
• Point d'éclair (°F): Not applicable
• Point d'éclair (°C): Not applicable