L-Glycerinaldehyd-3-phosphat -Lösung

Name: <SC>L</SC>-Glycerinaldehyd-3-phosphat -Lösung
Brand: SIGMA

≥95% (TLC), 8-12 mg/mL in H₂O (qNMR)

Synonym(e):

(2S)-2-Hydroxy-3-phosphonooxypropanal, L-GAP

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Über diesen Artikel

Empirische Formel (Hill-System):

C₃H₇O₆P

CAS-Nummer:

20283-52-7

Molekulargewicht:

170.06

NACRES:

NA.25

PubChem Substance ID:

329761564

UNSPSC Code:

12352201

MDL number:

MFCD28016587

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Produktname

L-Glycerinaldehyd-3-phosphat -Lösung, ≥95% (TLC), 8-12 mg/mL in H₂O (qNMR)

InChI

1S/C3H7O6P/c4-1-3(5)2-9-10(6,7)8/h1,3,5H,2H2,(H2,6,7,8)/t3-/m1/s1

SMILES string

[H]C([C@@H](O)COP(O)(O)=O)=O

InChI key

LXJXRIRHZLFYRP-GSVOUGTGSA-N

assay

≥95% (TLC)

form

liquid

concentration

8-12 mg/mL in H₂O (qNMR)

impurities

≤0.5 mg/mL D-glyceraldehyde-3-phosphate (enzymatic)

storage temp.

−20°C

Quality Level

100

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Dieser Artikel	39705	G5251	SML2709
Sigma-Aldrich 69312 L-Glycerinaldehyd-3-phosphat -Lösung	Sigma-Aldrich 39705 D-Glyceraldehyd-3-phosphat -Lösung	Sigma-Aldrich G5251 DL-Glyceraldehyd-3-phosphat -Lösung	Sigma-Aldrich SML2709 Sphingosine 1-phosphate ready made solution
assay ≥95% (TLC)	assay ≥97.0% (TLC)	assay -	assay ≥95% (TLC)
Quality Level 100	Quality Level 100	Quality Level 200	Quality Level 100
form liquid	form solution	form liquid	form liquid
storage temp. −20°C	storage temp. −20°C	storage temp. −20°C	storage temp. −20°C
impurities ≤0.5 mg/mL D-glyceraldehyde-3-phosphate (enzymatic)	impurities -	impurities -	impurities -
concentration 8-12 mg/mL in H₂O (qNMR)	concentration 8-13 mg/mL in H₂O	concentration 45-55 mg/mL in H₂O	concentration -

Biochem/physiol Actions

L-Glyceraldehyde 3-phosphate is a potent non-competitive inhibitor of NADP-dependent non-phosphorylating D-glyceraldehyde-3-phosphate dehydrogenase[1] and a substrate for L-Glyceraldehyde 3-phosphate reductase.

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.

Lagerklasse

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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The uncatalyzed rates of enolization of dihydroxyacetone phoshate and of glyceraldehyde 3-phosphate in neutral aqueous solution. The quantitative assessment of the effectiveness of an enzyme catalyst.

A Hall et al.

Biochemistry, 14(19), 4348-4353 (1975-09-23)

By a combination of methods involving enzyme-catalyzed reactions and classical iodination techniques it has been possible to obtain all the relevant rate constants for the uncatalyzed interconversion of dihydroxyacetone phosphate and D-glyceraldehyde 3-phosphate via their common enediol intermediate. These rate

L-Glyceraldehude 3-phosphate, a bactericidal agent.

C T Tang et al.

Antimicrobial agents and chemotherapy, 11(1), 147-153 (1977-01-01)

At a concentration of 2.5 mM, dl-glyceraldehyde 3-phosphate has a bactericidal effect upon Escherichia coli. The glycerol 3-phosphate transport system is required for the entry of the biologically active l-enantiomer. l-Glyceraldehyde must be phosphorylated by the cell to exert its

Purification and properties of NADP-dependent non-phosphorylating glyceraldehyde-3-phosphate dehydrogenase from the green alga Chlamydomonas reinhardtii.

Iglesias, A.A., et al.

Biochimica et Biophysica Acta, 925, 1-10 (1987)

L-glyceraldehyde 3-phosphate reductase from Escherichia coli is a heme binding protein.

Kevin K Desai et al.

Bioorganic chemistry, 38(1), 37-41 (2009-12-18)

Recently, we reported that YghZ from Escherichia coli functions as an efficient L-glyceraldehyde 3-phosphate reductase (Gpr). Here we show that Gpr co-purifies with a b-type heme cofactor. Gpr associates with heme in a 1:1 stoichiometry to form a complex that

Reaction of triosephosphate isomerase with L-glyceraldehyde 3-phosphate and triose 1,2-enediol 3-phosphate.

J P Richard

Biochemistry, 24(4), 949-953 (1985-02-12)

Triosephosphate isomerase catalyzes the isomerization and/or racemization reactions of L-glyceraldehyde 3-phosphate (LGAP), the enantiomer of the physiological substrate. The reaction is inhibited by the active site directed reagent glycidol phosphate. The amount of protonation product formation catalyzed by a fixed

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L-Glycerinaldehyd-3-phosphat -Lösung