C7505

L-Cystathionine

≥98% (TLC), suitable for UHPLC

• Sinónimos: (R)-S-(2-Amino-2-carboxyethyl)-L-homocysteine
• Fórmula empírica (notación de Hill): C₇H₁₄N₂O₄S
• Número de CAS: 56-88-2
• Peso molecular: 222.26
• Beilstein: 2505200
• Número CE: 200-295-8
• Número MDL: MFCD00036685
• Código UNSPSC: 12352209
• ID de la sustancia en PubChem: 24892965
• NACRES: NA.26

Propiedades

• Nombre del producto: L-Cystathionine, ≥98% (TLC)
• Nivel de calidad: 200
• Ensayo: ≥98% (TLC)
• Formulario: powder
• técnicas: UHPLC: suitable
• color: white
• mp: >300 °C
• temp. de almacenamiento: −20°C
• cadena 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
• Clave InChI: ILRYLPWNYFXEMH-WHFBIAKZSA-N

Descripción

Aplicación

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]

Acciones bioquímicas o fisiológicas

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]

Información de seguridad

• Código de clase de almacenamiento: 11 - Combustible Solids
• Clase de riesgo para el agua (WGK): WGK 3
• Punto de inflamabilidad (°F): Not applicable
• Punto de inflamabilidad (°C): Not applicable
• Equipo de protección personal: Eyeshields, Gloves, type N95 (US)