G0903

γ-Glu-Cys

≥80% (HPLC), suitable for ligand binding assays

• Sinónimos: γ-L-Glutamyl-L-cysteine, des-Gly-glutathione reduced form
• Fórmula empírica (notación de Hill): C₈H₁₄N₂O₅S
• Número CAS: 636-58-8
• Peso molecular: 250.27
• UNSPSC Code: 12352209
• PubChem Substance ID: 24895030
• NACRES: NA.26
• MDL number: MFCD00237863

Propiedades

• Nombre del producto: γ-Glu-Cys, ≥80% (HPLC)
• Quality Segment: 200
• assay: ≥80% (HPLC)
• form: powder
• composition: Peptide content, ≥60% elemental analysis
• technique(s): ligand binding assay: suitable
• color: white to off-white
• storage temp.: −20°C
• SMILES string: N[C@@H](CCC(=O)N[C@@H](CS)C(O)=O)C(O)=O
• InChI: 1S/C8H14N2O5S/c9-4(7(12)13)1-2-6(11)10-5(3-16)8(14)15/h4-5,16H,1-3,9H2,(H,10,11)(H,12,13)(H,14,15)/t4-,5-/m0/s1
• InChI key: RITKHVBHSGLULN-WHFBIAKZSA-N

Descripción

Application

γ-Glu-Cys is used to study the active sites and kinetics of glutathione synthetase(s). It has also been used for the extraction and quantification of low molecular weight thiols from Arabidopsis tissues.

Biochem/physiol Actions

γ-L-Glutamyl-L-cysteine (γ-Glu-Cys) is a substrate used for the biosynthesis of L-glutathione by glutathione synthetase(s). γ-Glu-Cys is generated by the cleavage of the Cys-Gly peptide bond of glutathione. It is also essential for the formation of phytochelatins, which are cysteine-rich thiol-reactive peptides.

Physical form

Lyophilized from 0.1% TFA.

Información de seguridad

• pictograms: GHS07
• signalword: Warning
• hcodes: H315,H319,H335
• pcodes: P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338
• Hazard Classifications: Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
• target_organs: Respiratory system
• Clase de almacenamiento: 11 - Combustible Solids
• wgk: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: dust mask type N95 (US), Eyeshields, Gloves