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Merck

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:
分子量:
230.02
Beilstein:
3767836
MDL號碼:
分類程式碼代碼:
12352201
PubChem物質ID:
NACRES:
NA.25

生物源

synthetic (inorganic)

品質等級

化驗

≥93% dry basis (enzymatic)

形狀

powder

環保替代產品特色

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

sustainability

Greener Alternative Product

雜質

<14% water (NMR)

顏色

white

溶解度

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

正離子痕跡

Na: 18-22% (dry basis)

環保替代類別

儲存溫度

−20°C

SMILES 字串

[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 密鑰

RGCJWQYUZHTJBE-YBBRRFGFSA-L

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相关类别

應用

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。

其他說明

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。

象形圖

Health hazardExclamation mark

訊號詞

Warning

危險分類

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

標靶器官

Eyes,Central nervous system, Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3


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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
Yinhua Zhang et al.
The Journal of biological chemistry, 279(35), 37185-37190 (2004-07-06)
Phosphoglycerate mutases catalyze the interconversion of 2- and 3-phosphoglycerate in the glycolytic and gluconeogenic pathways. They exist in two unrelated forms that are either cofactor (2,3-diphosphoglycerate)-dependent or cofactor-independent. The two enzymes have no similarity in amino acid sequence, tertiary structure
Maria V Liberti et al.
Cell metabolism, 26(4), 648-659 (2017-09-19)
Targeted cancer therapies that use genetics are successful, but principles for selectively targeting tumor metabolism that is also dependent on the environment remain unknown. We now show that differences in rate-controlling enzymes during the Warburg effect (WE), the most prominent

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