2319882-36-3
2319882-36-3
Chemical Structure
(R)-(-)-Citramalic acid lithium
Synonym(s): (R)-Citramalate lithium; (2R)-Methylmalic acid lithium
- CAS No.: 2319882-36-3
- Formula:C5H7LiO5
- Molecular Weight:154.05
SMILES: O=C(O[Li])C[C@@](C)(O)C(O)=O
Biological Activity: (R)-(-)-Citramalic acid ((R)-Citramalate) lithium, a lithium salt of Citramalic acid, is the R enantiomer of Citramalic acid lithium. (R)-(-)-Citramalic acid lithium is involved in the metabolism of glutamate through the methylaspartate pathway. (R)-(-)-Citramalic acid lithium is promising for research of neurological disorders[1][2][3].
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(R)-(-)-Citramalic acid lithium | (R)-(-)-Citramalic acid ((R)-Citramalate) lithium, a lithium salt of Citramalic acid, is the R enantiomer of Citramalic acid lithium. (R)-(-)-Citramalic acid lithium is involved in the metabolism of glutamate through the methylaspartate pathway. (R)-(-)-Citramalic acid lithium is promising for research of neurological disorders. | |||||||||||||||||||||
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References
- [1]. Whitesell J K, et al. Observations on the reactions of chiral pyruvates. Synthesis of (-)-and (+)-citramalic acid[J]. The Journal of Organic Chemistry, 1989, 54(9): 2258-2260.
- [2]. Howell DM, et al. (R)-citramalate synthase in methanogenic archaea. J Bacteriol. 1999 Jan;181(1):331-3. [Content Brief]
- [3]. Gill M, et al. Pigments of fungi. LIX. Synthesis of (1S, 3S)-and (1R, 3R)-austrocortilutein and (1S, 3S)-austrocortirubin from citramalic acid[J]. Australian Journal of Chemistry, 2000, 53(4): 245-256.
Keywords
