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Merck
CN

51269

Sigma-Aldrich

二羟丙酮磷酸盐 半镁盐 水合物

≥95% (TLC)

别名:

1,3-二羟基-2-丙酮1-磷酸酯 半镁盐, 1-羟基-3-(膦酰氧基)-2-丙酮 半镁盐, DHAP 镁

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关于此项目

经验公式(希尔记法):
C3H5Mg0.5O6P · xH2O
化学文摘社编号:
分子量:
180.19 (anhydrous basis)
MDL编号:
UNSPSC代码:
12352107
PubChem化学物质编号:
NACRES:
NA.25
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质量水平

方案

≥95% (TLC)

储存温度

−20°C

SMILES字符串

O.OCC(=O)COP(O)(=O)O[Mg]OP(O)(=O)OCC(=O)CO

InChI

1S/2C3H7O6P.Mg.H2O/c2*4-1-3(5)2-9-10(6,7)8;;/h2*4H,1-2H2,(H2,6,7,8);;1H2/q;;+2;/p-2

InChI key

XIBMKSGIYJARCI-UHFFFAOYSA-L

相关类别

应用

磷酸二羟乙基镁镁盐水合物(DHAP Mg)是DHAP的镁盐。DHAP可作为表征果糖二磷酸醛缩酶和磷酸丙糖替代酶等酶的底物。

生化/生理作用

磷酸二羟丙酮(DHAP)是一种参与到多种通路中的代谢中间体,包括糖酵解、糖异生、甘油代谢、磷脂酸合成、脂肪代谢和卡尔文循环。

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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An efficient gram scale synthesis of 3-fluoro-1-hydroxyacetone phosphate (FHAP) has been developed. As a close analog to dihydroxyacetone phosphate, FHAP was used as a novel donor substrate for rabbit muscle aldolase catalyzed reactions. The different binding affinities of the gem-diol
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The FEBS journal, 279(23), 4410-4420 (2012-10-18)
Coherent glycolytic oscillations in Saccharomyces cerevisiae are a multicellular property induced by addition of glucose to a starved cell population of sufficient density. However, initiation of oscillations requires an additional perturbation, usually addition of cyanide. The fate of cyanide during
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Gold nanoparticles (AuNPs) are attractive materials for the immobilization of enzymes due to several advantages such as high enzyme loading, absence of internal diffusion limitations, and Brownian motion in solution, compared to the conventional immobilization onto porous macroscopic supports. The
Matthias Bujara et al.
Nature chemical biology, 7(5), 271-277 (2011-03-23)
Recruiting complex metabolic reaction networks for chemical synthesis has attracted considerable attention but frequently requires optimization of network composition and dynamics to reach sufficient productivity. As a design framework to predict optimal levels for all enzymes in the network is
Alice Chan et al.
Angewandte Chemie (International ed. in English), 51(31), 7711-7714 (2012-06-21)
Stop for NadA! A [4Fe-4S] enzyme, NadA, catalyzes the formation of quinolinic acid in de novo nicotinamide adenine dinucleotide (NAD) biosynthesis. A structural analogue of an intermediate, 4,5-dithiohydroxyphthalic acid (DTHPA), has an in vivo NAD biosynthesis inhibiting activity in E. coli. The

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