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Merck
CN

39584

3-Sulfopyruvic acid lithium salt hydrate

≥97.0% (TLC)

Synonym(s):

2-Oxo-3-sulfopropanoic acid lithium salt hydrate, Lithium 3-sulfopyruvate hydrate

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About This Item

Empirical Formula (Hill Notation):
C3H4O6S
Molecular Weight:
168.13
NACRES:
NA.24
PubChem Substance ID:
UNSPSC Code:
41116107
MDL number:
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InChI key

BUTHMSUEBYPMKJ-UHFFFAOYSA-N

SMILES string

O=C(C(O)=O)CS(=O)(O)=O

InChI

1S/C3H4O6S/c4-2(3(5)6)1-10(7,8)9/h1H2,(H,5,6)(H,7,8,9)

grade

analytical standard

assay

≥97.0% (TLC)

impurities

≤15% water

format

neat

storage temp.

2-8°C

Quality Level

Biochem/physiol Actions

3-Sulfopyruvic acid is the product of the transamination of cysteinesulfonate in a reaction catalyzed by aspartate amino- transferase. 3-Sulfopyruvic acid is stable and is reduced by malate dehydrogenase to beta-sulfolactate, which is excreted in the urine. Cysteinesulfonate, 3-sulfo- pyruvic acid, and beta-sulfolactate are reversibly interconverted in vivo.

Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Israel, M.
Cancer Therapy, 10, 1-1 (2014)
Mammalian sulfur amino acid metabolism: an overview.
O W Griffith
Methods in enzymology, 143, 366-376 (1987-01-01)
C L Weinstein et al.
The Journal of biological chemistry, 263(8), 3735-3743 (1988-03-15)
L-Cysteinesulfonate (L-cysteate) is present in plasma, urine, and tissues in concentrations comparable to that of L-cysteinesulfinate, the primary oxidative metabolite of L-cysteine. Although cysteinesulfonate is known to be decarboxylated to taurine by cysteinesulfinate decarboxylase, the occurrence and importance of other
Three rare diseases in one Sib pair: RAI1, PCK1, GRIN2B mutations associated with Smith-Magenis Syndrome, cytosolic PEPCK deficiency and NMDA receptor glutamate insensitivity.
Adams DR, Yuan H, Holyoak T, et al.
Molecular Genetics and Metabolism, 113(3), 161-170 (2014)
Molecular properties of dihydropyridine-sensitive calcium channels in skeletal muscle.
W A Catterall et al.
The Journal of biological chemistry, 263(8), 3535-3538 (1988-03-15)

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