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39705

Sigma-Aldrich

D-Glyceraldehyde 3-phosphate solution

8-13 mg/mL in H2O

Synonym(s):

(2R)-2-Hydroxy-3-phosphonooxypropanal, D-GAP, Triose phosphate

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About This Item

Empirical Formula (Hill Notation):
C3H7O6P
CAS Number:
591-57-1
Molecular Weight:
170.06
Beilstein:
1725007
MDL number:
MFCD23703755
UNSPSC Code:
12352201
PubChem Substance ID:
329755894
NACRES:
NA.25

Assay

≥97.0% (TLC)

Quality Level

100

form

solution

concentration

8-13 mg/mL in H2O

color

colorless

storage temp.

−20°C

SMILES string

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

InChI

1S/C3H7O6P/c4-1-3(5)2-9-10(6,7)8/h1,3,5H,2H2,(H2,6,7,8)/t3-/m0/s1

InChI key

LXJXRIRHZLFYRP-VKHMYHEASA-N

Application


  • Enzymatic Assay Development with d-Glyceraldehyde 3-Phosphate: Demonstrated as a crucial reagent in enzymatic assays involving glycolysis pathways, specifically in the assessment of glyceraldehyde 3-phosphate dehydrogenase activities, which play a vital role in understanding cellular energy production and metabolic disorders (Li et al., 2022).

Biochem/physiol Actions

An important substance implicated in energy metabolism. It is a key node point linking other metabolic processes or pathways. Triosephosphate metabolism can be associated with many metabolic pathways, including glycolysis, pentose phosphate pathway, gluconeogenesis and lipid metabolism, and can also be involved in maintaining hemostasis. The metabolic abnormality of triosephosphate may be tied to many pathophysiological processes, such as triosephosphate isomerase deficiency, hyperglycemia and diabetic nephropathy; review and papers cited therein.

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.

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

39705-1ML:
39705-BULK:
39705-VAR:
39705-5ML:

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Certificates of Analysis (COA)

Lot/Batch Number
BCCK0151
BCCG3064
BCCB6517
BCBW5537
BCBR1821V

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Raul Mendez et al.
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Life (Basel, Switzerland), 10(3) (2020-03-19)
The halotolerant cyanobacterium, Halothece sp. PCC 7418, possesses two classes of fructose-1,6-bisphosphate aldolase (FBA): H2846 and H2847. Though class I (CI)-FBA H2846 is thought to be associated with salt tolerance, the regulatory mechanisms, molecular characteristics, and expression profiles between H2846
Ruilian Yao et al.
Microbial cell factories, 10, 67-67 (2011-08-13)
Most bacteria can use various compounds as carbon sources. These carbon sources can be either co-metabolized or sequentially metabolized, where the latter phenomenon typically occurs as catabolite repression. From the practical application point of view of utilizing lignocellulose for the
Amparo C Villablanca et al.
SpringerPlus, 2(1), 214-214 (2013-06-07)
Vascular endothelium expresses both the estrogen receptors (ERs) α and β, and ERα mediates development of early atherosclerosis in male mice. This process is thought to be testosterone-dependent. We hypothesized that male murine aortic endothelium produces robust levels of estradiol
Rebeca Arroyo Hornero et al.
Communications biology, 3(1), 375-375 (2020-07-16)
Regulatory T cells (Tregs) are critical mediators of immune homeostasis. The co-stimulatory molecule CD27 is a marker of highly suppressive Tregs, although the role of the CD27-CD70 receptor-ligand interaction in Tregs is not clear. Here we show that after prolonged
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