C7505

L-Cystathionine

≥98% (TLC), suitable for UHPLC

• Synonyme(s) : (R)-S-(2-Amino-2-carboxyethyl)-L-homocysteine
• Formule empirique (notation de Hill) : C₇H₁₄N₂O₄S
• Numéro CAS: 56-88-2
• Poids moléculaire : 222.26
• Beilstein: 2505200
• Numéro CE : 200-295-8
• Numéro MDL: MFCD00036685
• Code UNSPSC : 12352209
• ID de substance PubChem : 24892965
• Nomenclature NACRES : NA.26

Propriétés

• Nom du produit: L-Cystathionine, ≥98% (TLC)
• Essai: ≥98% (TLC)
• Forme: powder
• Technique(s): UHPLC: suitable
• Couleur: white
• Pf: >300 °C
• Température de stockage: −20°C
• Chaîne SMILES: N[C@@H](CCSC[C@H](N)C(O)=O)C(O)=O
• InChI: 1S/C7H14N2O4S/c8-4(6(10)11)1-2-14-3-5(9)7(12)13/h4-5H,1-3,8-9H2,(H,10,11)(H,12,13)/t4-,5-/m0/s1
• Clé InChI: ILRYLPWNYFXEMH-WHFBIAKZSA-N

Description

Application

L-Cystathionine has been used in ultra-performance liquid chromatography for the validation of cystathionine and the correlation of its abundance with vertebrate metamorphosis. It has also been used as an inhibitor of sinusoidal GSH (glutathione) carrier to signify that thiol redox state imbalance is associated with the modulation of autophagy in carcinoma cells.[1]

Actions biochimiques/physiologiques

L-Cystathionine is an intermediate in the biosynthesis of L-cysteine and methionine.[2][3] It is used as a substrate to differentiate and analyze cystathionine γ-lyase(s).[4] L-Cystathionine is an important non-protein amino acid and is associated with metabolic disorders.[5] In recent studies, L-cystathionine is believed to be the precursor of cyclic imino acid cyclothionine. Cystathioninuria is characterized with imino acid cyclothionine excretion in the urine.[3]

Informations sur la sécurité

• Code de la classe de stockage: 11 - Combustible Solids
• Classe de danger pour l'eau (WGK): WGK 3
• Point d'éclair (°F): Not applicable
• Point d'éclair (°C): Not applicable
• Équipement de protection individuelle: Eyeshields, Gloves, type N95 (US)