61786
D-甘油酸钠盐 钠盐
≥95.0% (TLC)
别名:
(R)-2,3-二羟基丙酸 钠盐, D -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
产品名称
D-甘油酸钠盐 钠盐, ≥95.0% (TLC)
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-/m1/s1
InChI key
RBNPOMFGQQGHHO-UWTATZPHSA-N
assay
≥95.0% (TLC)
form
powder or crystals
optical activity
[α]/D 18.5±3.0°, c = 1 in water
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
Theresa Kouril et al.
The FEBS journal, 280(4), 1126-1138 (2013-01-03)
Sulfolobus solfataricus P2 is a thermoacidophilic archaeon that metabolizes glucose and galactose via an unusual branched Entner-Doudoroff (ED) pathway, which is characterized by a non-phosphorylative (np) and a semi-phosphorylative (sp) branch. However, so far the physiological significance of the two
J D Goldberg et al.
Journal of molecular biology, 236(4), 1123-1140 (1994-03-04)
D-Glycerate dehydrogenase (GDH) catalyzes the NADH-linked reduction of hydroxypyruvate to D-glycerate. GDH is a member of a family of NAD-dependent dehydrogenases that is characterized by a specificity for the D-isomer of the hydroxyacid substrate. The crystal structure of the apoenzyme
S K Wadman et al.
Clinica chimica acta; international journal of clinical chemistry, 71(3), 477-484 (1976-09-20)
A patient is described with glyceric acidemia and glyceric aciduria. The main clinical problems in infancy were severe metabolic acidosis and failure to thrive. The patient needs permanent treatment with bicarbonate. Hyperglycinemia, as described in the first case discovered elsewhere
E Van Schaftingen
FEBS letters, 243(2), 127-131 (1989-01-30)
D-Glycerate kinase was measured in human livers thanks to a new, sensitive radiochemical assay. The enzyme was extremely unstable in extracts prepared in water, but was partly stabilized in a homogenization mixture containing inorganic phosphate, D-glycerate and EGTA. When extracted
Jörn Oliver Sass et al.
Human mutation, 31(12), 1280-1285 (2010-10-16)
D-glyceric aciduria is a rare inborn error of serine and fructose metabolism that was first described in 1974. Most affected individuals have presented with neurological symptoms. The molecular basis of D-glyceric aciduria is largely unknown; possible causes that have been
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