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72764

Sigma-Aldrich

2-Phosphoglycolic acid lithium salt

≥95.0% (HPLC)

Sinónimos:

2-(Phosphonooxy)acetic acid lithium salt, Glycolic acid phosphate lithium salt, Lithium phosphoglycolate

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About This Item

Fórmula empírica (notación de Hill):
C2H5O6P · xLi+
Número de CAS:
13147-57-4
Peso molecular:
156.03 (free acid basis)
Beilstein/REAXYS Number:
1773480
UNSPSC Code:
12352204
NACRES:
NA.32

assay

≥95.0% (HPLC)

form

powder or crystals

storage temp.

−20°C

InChI

1S/C2H5O6P/c3-2(4)1-8-9(5,6)7/h1H2,(H,3,4)(H2,5,6,7)

InChI key

ASCFNMCAHFUBCO-UHFFFAOYSA-N

Biochem/physiol Actions

Manifold links of photo-respiration to central metabolism, 2-phospho-glycolate content of tissues.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Hermann Bauwe et al.
Current opinion in plant biology, 15(3), 269-275 (2012-01-31)
Photorespiration is a Janus-headed metabolic process: it makes oxygenic photosynthesis possible by scavenging its major toxic by-product, 2-phosphoglycolate, but also leads to high losses of freshly assimilated CO(2) from most land plants. Photorespiration has been often classified as a wasteful
John Knight et al.
Analytical biochemistry, 421(1), 121-124 (2011-11-19)
Glycolate and 2-phosphoglycolate (PG) are 2-carbon monocarboxylic acids with ill-defined metabolic roles. Their concentrations have not yet been described in tissues apart from body fluids and erythrocytes. We describe the use of ion chromatography coupled with mass spectrometry (IC-MS) to
Iris N Serratos et al.
Journal of molecular biology, 405(1), 158-172 (2010-10-26)
Electrostatic interactions have a central role in some biological processes, such as recognition of charged ligands by proteins. We characterized the binding energetics of yeast triosephosphate isomerase (TIM) with phosphorylated inhibitors 2-phosphoglycollate (2PG) and phosphoglycolohydroxamate (PGH). We determined the thermodynamic

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