72764
2-Phosphoglycolic acid lithium salt
≥95.0% (HPLC)
Synonym(s):
2-(Phosphonooxy)acetic acid lithium salt, Glycolic acid phosphate lithium salt, Lithium phosphoglycolate
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About This Item
Empirical Formula (Hill Notation):
C2H5O6P · xLi+
CAS Number:
Molecular Weight:
156.03 (free acid basis)
Beilstein:
1773480
UNSPSC Code:
12352204
NACRES:
NA.32
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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 Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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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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