51738
L-甘油酸 钠盐
≥95.0% (TLC)
别名:
(S)-2,3-二羟基丙酸 钠盐, L-甘油酸钠
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关于此项目
经验公式（希尔记法）:
C3H6O4 · xNa+
化学文摘社编号:
分子量:
106.08 (free acid basis)
MDL number:
UNSPSC Code:
12352201
NACRES:
NA.25
SMILES string
O[C@@H](CO)C(=O)O
InChI
1S/C3H6O4/c4-1-2(5)3(6)7/h2,4-5H,1H2,(H,6,7)/t2-/m0/s1
InChI key
RBNPOMFGQQGHHO-REOHCLBHSA-N
assay
≥95.0% (TLC)
form
powder or crystals
optical activity
[α]/D -18.5±3.0°, c = 1 in H2O
color
white
Quality Level
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存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Pierre Cochat et al.
Pediatric nephrology (Berlin, Germany), 25(3), 415-424 (2009-01-22)
Nephrolithiasis associated with inborn metabolic diseases is a very rare condition with some common characteristics: early onset of symptoms, family history, associated tubular impairment, bilateral, multiple and recurrent stones, and association with nephrocalcinosis. The prognosis of such diseases may lead
Eduardo Salido et al.
Biochimica et biophysica acta, 1822(9), 1453-1464 (2012-03-27)
Glyoxylate detoxification is an important function of human peroxisomes. Glyoxylate is a highly reactive molecule, generated in the intermediary metabolism of glycine, hydroxyproline and glycolate mainly. Glyoxylate accumulation in the cytosol is readily transformed by lactate dehydrogenase into oxalate, a
C J Danpure et al.
Journal of inherited metabolic disease, 12(4), 403-414 (1989-01-01)
This paper concerns an enzymological investigation into a putative feline analogue of the human autosomal recessive disease primary hyperoxaluria type 2. The hepatic activities of D-glycerate dehydrogenase, using both D-glycerate and hydroxypyruvate as substrates, and glyoxylate reductase, which are the
Identification and location of L-glycerate, an unusual acyl substituent in gellan gum.
Kuo, M.S. and Mort, A.J.
Carbohydrate Research, 156, 173-187 (1986)
Mohamed S Rashed et al.
Biomedical chromatography : BMC, 16(3), 191-198 (2002-03-29)
Glyceric acid is a highly polar chiral carboxylic acid that is usually not detected during routine organic acid analysis. Increased excretion is observed in two phenotypically distinct and rare inherited metabolic diseases, D-glyceric aciduria, and L-glyceric aciduria (also known as
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