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D7137

Dihydroxyacetonphosphat Dilithiumsalz

≥93% dry basis (enzymatic)

Synonym(e):

1,3-Dihydroxy-2-propanon-1-phosphat Dilithiumsalz, 1-Hydroxy-3-(phosphonooxy)-2-propanon Dilithiumsalz, DHAP

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Über diesen Artikel

Empirische Formel (Hill-System):
C3H5Li2O6P
CAS-Nummer:
102783-56-2
Molekulargewicht:
181.92
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
24894082
MDL number:
MFCD00077731
Beilstein/REAXYS Number:
1708891

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InChI

1S/C3H7O6P.2Li/c4-1-3(5)2-9-10(6,7)8;;/h4H,1-2H2,(H2,6,7,8);;/q;2*+1/p-2

SMILES string

[Li+].[Li+].OCC(=O)COP([O-])([O-])=O

InChI key

QWIKESRFRWLYIA-UHFFFAOYSA-L

biological source

bovine (casein)

assay

≥93% dry basis (enzymatic)

form

powder

impurities

~0.2 mol % D-glyceraldehyde 3-phosphate

color

white

solubility

soluble 50mg plus 1ml of H2O, clear, colorless to faintly yellow

anion traces

phosphate (PO43-): ~5 mol %

cation traces

Li: 5.5-8.0% (dry basis)

storage temp.

−20°C

Quality Level

200

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Dieser Artikel
3744251269P7002
Dihydroxyacetone phosphate dilithium salt ≥93% dry basis (enzymatic)

Sigma-Aldrich

D7137

Dihydroxyacetone phosphate dilithium salt

Dihydroxyacetone phosphate lithium salt ≥95.0% (TLC)

Sigma-Aldrich

37442

Dihydroxyacetone phosphate lithium salt

Dihydroxyacetone phosphate hemimagnesium salt hydrate ≥95% (TLC)

Sigma-Aldrich

51269

Dihydroxyacetone phosphate hemimagnesium salt hydrate

Phospho(enol)pyruvic acid trisodium salt hydrate ≥97% (enzymatic)

Sigma-Aldrich

P7002

Phospho(enol)pyruvic acid trisodium salt hydrate

assay

≥93% dry basis (enzymatic)

assay

≥95.0% (TLC)

assay

≥95% (TLC)

assay

≥97% (enzymatic)

biological source

bovine (casein)

biological source

-

biological source

-

biological source

-

solubility

soluble 50mg plus 1ml of H2O, clear, colorless to faintly yellow

solubility

-

solubility

-

solubility

water: 100 mg/mL, clear to slightly hazy, colorless to very faintly yellow

Quality Level

200

Quality Level

100

Quality Level

100

Quality Level

200

form

powder

form

powder

form

-

form

powder

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

Application

Dihydroxyacetone phosphate (DHAP) is used in fructose metabolism, triose and glycation research. It is used in studies involving the metabolism of three-carbon sugar pools and their roles in physiological and physical processes.[1] DHAP may be used as a substrate to help identify, differentiate and characterize fructose-bisphosphate aldolase(s) (ALDOA) and triosephosphate isomerase(s).[2] DHAP may be used to study cellular glycation stress.[3]

Biochem/physiol Actions

A metabolic intermediate involved in many pathways, including glycolysis and the Calvin cycle.
Dihydroxyacetone phosphate (DHAP) is a metabolic intermediate involved in many pathways, including glycolysis, gluconeogenesis, glycerol metabolism, phosphatidic acid synthesis, fat metabolism, and the Calvin cycle.

Preparation Note

Enzymatically prepared.

Other Notes

To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Disclaimer

Unlike the dimethyl ketal, does not require hydrolysis prior to use as a substrate.

Lagerklasse

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
0000443468
0000443466
0000443466
0000443468
0000439147

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Saheem Ahmad et al.
PloS one, 8(9), e72128-e72128 (2013-09-12)
Non-enzymatic glycation is the addition of free carbonyl group of reducing sugar to the free amino groups of proteins, resulting in the formation of a Schiff base and an Amadori product. Dihydroxyacetone (DHA) is one of the carbonyl species which
Chiara Fania et al.
PloS one, 12(6), e0179280-e0179280 (2017-06-20)
In the diagnosis of Alzheimer's disease (AD) total tau (T-tau), tau phosphorylated at threonine 181 (P-tau181), and the 42 amino acid isoform of alpha β-amyloid (Aβ) are well established surrogate CSF markers. However, there is a constant need for new
Daisuke Takagi et al.
Plant & cell physiology, 55(2), 333-340 (2014-01-11)
Sugar-derived reactive carbonyls (RCs), including methylglyoxal (MG), are aggressive by-products of oxidative stress known to impair the functions of multiple proteins. These advanced glycation end-products accumulate in patients with diabetes mellitus and cause major complications, including arteriosclerosis and cardiac insufficiency.
Sebastien Elis et al.
Journal of ovarian research, 10(1), 74-74 (2017-11-11)
Supplementation of bovine oocyte-cumulus complexes during in vitro maturation (IVM) with 1 μM of docosahexaenoic acid (DHA), C22:6 n-3 polyunsaturated fatty acid, was reported to improve in vitro embryo development. The objective of this paper was to decipher the mechanisms of
Pol Arranz-Gibert et al.
Scientific reports, 8(1), 6446-6446 (2018-04-25)
Peptides are experiencing a new era in medical research, finding applications ranging from therapeutics to vaccines. In spite of the promising properties of peptide pharmaceuticals, their development continues to be hindered by three weaknesses intrinsic to their structure, namely protease
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