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P8877

Sigma-Aldrich

D-(−)-3-磷酸甘油酸 二钠盐

greener alternative

≥93% dry basis (enzymatic), powder

别名:

(−)-二钠-D-3-磷酸甘油酸, D-甘油三磷酸盐 二钠盐

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About This Item

经验公式（希尔记法）:
C3H5Na2O7P
CAS号:
80731-10-8
分子量:
230.02
Beilstein:
3767836
MDL编号:
MFCD00069569
UNSPSC代码:
12352201
PubChem化学物质编号:
24898988
NACRES:
NA.25

生物来源

synthetic (inorganic)

质量水平

200

方案

≥93% dry basis (enzymatic)

表单

powder

环保替代产品特性

Atom Economy
Design for Energy Efficiency
Use of Renewable Feedstocks
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

杂质

<14% water (NMR)

颜色

white

溶解性

H2O: 50 mg/mL, clear, colorless to faintly yellow

痕量阳离子

Na: 18-22% (dry basis)

环保替代产品分类

Re-engineered,

储存温度

−20°C

SMILES字符串

[Na+].[Na+].O[C@H](COP(O)([O-])=O)C([O-])=O

InChI

1S/C3H7O7P.2Na/c4-2(3(5)6)1-10-11(7,8)9;;/h2,4H,1H2,(H,5,6)(H2,7,8,9);;/q;2*+1/p-2/t2-;;/m1../s1

InChI key

RGCJWQYUZHTJBE-YBBRRFGFSA-L

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相关类别

应用

在研究中D-（-）-3-磷酸甘油酸二钠盐已用于评估水溶液中甘油酸的磷酸化。 在研究中，它还被用于表征谷胱甘肽和NAD依赖的与糖酵解相关的砷酸盐还原。

生化/生理作用

3-磷酸甘油酸是糖酵解中的中间体。它也是丝氨酸形成的前体。

其他说明

为了全面了解我们针对客户研究提供的各种单糖产品，建议您访问我们的碳水化合物分类页面。

象形图

Health hazardExclamation mark
GHS08,GHS07

警示用语：

Warning

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 2 - STOT SE 3

靶器官

Eyes,Central nervous system, Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
0000399555
0000369134
0000356750
0000355373
0000324300

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Balázs Németi et al.
Toxicological sciences : an official journal of the Society of Toxicology, 85(2), 847-858 (2005-03-25)
Reduction of arsenate (AsV) to the more toxic arsenite (AsIII) is of high toxicological importance, yet in vivo relevant enzymes involved have not been identified. Purine nucleoside phosphorylase (PNP) is an efficient AsV reductase in vitro, but its role in
V Kolb et al.
Origins of life and evolution of the biosphere : the journal of the International Society for the Study of the Origin of Life, 26(1), 7-13 (1996-02-01)
The phosphorylation of glyceric acid is an interesting prebiotic reaction because it converts a simple, potentially prebiotic organic molecule into phosphate derivatives that are central to carbohydrate metabolism. We find that 0.05 M glyceric acid in the presence of 0.5
Jeremy M Foster et al.
PloS one, 5(10), e13576-e13576 (2010-12-29)
The glycolytic phosphoglycerate mutases exist as non-homologous isofunctional enzymes (NISE) having independent evolutionary origins and no similarity in primary sequence, 3D structure, or catalytic mechanism. Cofactor-dependent PGM (dPGM) requires 2,3-bisphosphoglycerate for activity; cofactor-independent PGM (iPGM) does not. The PGM profile
Jeremy M Foster et al.
Parasitology research, 104(5), 1047-1052 (2008-12-02)
Phosphoglycerate mutases (PGM) interconvert 2- and 3-phosphoglycerate in the glycolytic and gluconeogenic pathways. A putative cofactor-independent phosphoglycerate mutase gene (iPGM) was identified in the genome sequence of the Wolbachia endosymbiont from the filarial nematode, Brugia malayi (wBm). Since iPGM has
Junji Okuda et al.
PloS one, 8(8), e72173-e72173 (2013-08-21)
Heart failure is associated with changes in cardiac energy metabolism. Glucose metabolism in particular is thought to be important in the pathogenesis of heart failure. We examined the effects of persistent overexpression of phosphoglycerate mutase 2 (Pgam2), a glycolytic enzyme
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