56-88-2
56-88-2
Chemical Structure
L-Cystathionine
- CAS No.: 56-88-2
- Formula:C7H14N2O4S
- Molecular Weight:222.26
IUPAC Name: S-((R)-2-amino-2-carboxyethyl)-L-homocysteine
InChIKey: ILRYLPWNYFXEMH-WHFBIAKZSA-N
SMILES: N[C@@H](CCSC[C@H](N)C(O)=O)C(O)=O
Biological Activity: L-Cystathionine is a nonprotein thioether and is a key amino acid associated with the metabolic state of sulfur-containing amino acids. L-Cystathionine protects against Homocysteine-induced mitochondria-dependent apoptosis of vascular endothelial cells (HUVECs). L-Cystathionine plays an important role in cardiovascular protection[1][2].
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L-Cystathionine | 99.91% | L-Cystathionine is a nonprotein thioether and is a key amino acid associated with the metabolic state of sulfur-containing amino acids. L-Cystathionine protects against Homocysteine-induced mitochondria-dependent apoptosis of vascular endothelial cells (HUVECs). L-Cystathionine plays an important role in cardiovascular protection. | ||||||||||||||||||||
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L-Cystathionine (Standard) | ≥98% | L-Cystathionine is a nonprotein thioether and is a key amino acid associated with the metabolic state of sulfur-containing amino acids. L-Cystathionine protects against Homocysteine-induced mitochondria-dependent apoptosis of vascular endothelial cells (HUVECs). L-Cystathionine plays an important role in cardiovascular protection. | ||||||||||||||||||||
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References
- [1]. Xiuli Wang, et al. L-Cystathionine Protects against Homocysteine-Induced Mitochondria-Dependent Apoptosis of Vascular Endothelial Cells. Oxid Med Cell Longev. 2019 Nov 25;2019:1253289. [Content Brief]
- [2]. Amino Y, et al. Synthesis and evaluation of L-cystathionine as a standard for amino acid analysis. Biosci Biotechnol Biochem. 2017 Jan;81(1):95-101. [Content Brief]
