D-Glyceraldehyde 3-phosphate
Based on 1 publication(s) in Google Scholar
D-Glyceraldehyde 3-phosphate (Triose phosphate) is a key intermediate in glycolysis and gluconeogenesis, as well as a carbohydrate product of the Calvin cycle. D-Glyceraldehyde 3-phosphate participates in the biosynthesis of tryptophan and thiamine. D-Glyceraldehyde 3-phosphate is released as an aldehyde under the action of aldolase or triosephosphate isomerase. D-Glyceraldehyde 3-phosphate forms adducts with thiols.
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- Purity: 99.84%
- CAS No.: 591-57-1
- Formula: C3H7O6P
- Molecular Weight:170.06
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Storage:
Solution, -20°C, 2 years
Publications Citing Use of MedChemExpress (MCE) D-Glyceraldehyde 3-phosphate
MoreAll Endogenous Metabolite Isoforms
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Biological Activity
Description
IC50 & Target
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Human Endogenous Metabolite |
In Vitro
D-Glyceraldehyde 3-phosphate serves as the direct substrate of the oxidative phosphorylation reaction catalyzed by GAPDH, which converts it into 1,3-bisphosphoglycerate. The binding and catalytic processes are mediated by the conserved active site region of GAPDH[1].
D-Glyceraldehyde 3-phosphate is mainly allocated to starch and sucrose synthesis in plants, with a small fraction shunted to secondary metabolic pathways, and its allocation to starch is strongly affected by photoperiod[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
In Vivo
D-Glyceraldehyde 3-phosphate utilization limitation is a dominant constraint on barley photosynthesis at 10°C, with exogenous phosphate feeding significantly restoring CO2 assimilation rates[2].
D-Glyceraldehyde 3-phosphate utilization for starch and sucrose synthesis in Arabidopsis shows strong photoperiod dependence, with significantly higher carbon partitioning to starch under short photoperiods[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 591-57-1
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Appearance Liquid
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Molecular Weight 170.06
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Formula C3H7O6P
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Color Colorless to light yellow
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SMILES
O=C[C@H](O)COP(O)(O)=O
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Synonyms
Triose phosphate
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Structure Classification
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Initial Source
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Solution, -20°C, 2 years
Publications (1)
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Journal Impact Factor
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Most Recent
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bioRxiv
Discovery of metabolites produced by reactions between central carbon metabolites and cysteine that mark inflammatory macrophages. [Abstract]2026 Mar 20:2026.03.18.712640. PMID: 41889857
Purity & Documentation
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Data Sheet (300 KB)
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SDS (393 KB)
- English - EN (393 KB)
- Français - FR (393 KB)
- Deutsch - DE (393 KB)
- Norwegian - NO (393 KB)
- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Korean - KR (393 KB)
- Portuguese - PT (393 KB)
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Handling Instructions (2659 KB)
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Keywords
- D-Glyceraldehyde 3-phosphate
- 591-57-1
- Triose
- Fructose-1,6-bisphosphate aldolase
- Endogenous Metabolite
- fructose catabolism
- glyceraldehyde-3-phosphate dehydrogenase
- Phaseolus vulgaris
- pentose phosphate pathway
- Calvin-Benson cycle intermediate
- glycolytic intermediate
- 1,3-bisphosphoglycerate
- C3 plants
- gluconeogenesis
- glycerol metabolism
- Inhibitor
- inhibitor
- inhibit