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Key Documents

61786

Sigma-Aldrich

D-甘油酸钠盐 钠盐

≥95.0% (TLC)

同義詞:

(R)-2,3-二羟基丙酸 钠盐, D -甘油酸钠

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About This Item

經驗公式(希爾表示法):
C3H6O4 · xNa+
CAS號碼:
分子量::
106.08 (free acid basis)
分類程式碼代碼:
12352201
NACRES:
NA.25

化驗

≥95.0% (TLC)

形狀

powder or crystals

光學活性

[α]/D 18.5±3.0°, c = 1 in water

顏色

white

InChI

1S/C3H6O4/c4-1-2(5)3(6)7/h2,4-5H,1H2,(H,6,7)/t2-/m1/s1

InChI 密鑰

RBNPOMFGQQGHHO-UWTATZPHSA-N

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其他說明

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儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析證明 (COA)

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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
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
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
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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