Molecular structure of Dihydroxyacetone phosphate dilithium salt, CAS Number: 102783-56-2
Dihydroxyacetone phosphate dilithium salt (CAS 102783-56-2)
See product citations (3)
Alternate Names:
Glycerone phosphate; DHAP
Application:
Dihydroxyacetone phosphate dilithium salt is a substrate for triosephosphate isomerase assays
CAS Number:
102783-56-2
Purity:
≥93%
Molecular Weight:
181.92
Molecular Formula:
C3H5O6P•2Li
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
Dihydroxyacetone phosphate dilithium salt is a substrate for triosephosphate isomerase assays. Dihydroxyacetone phosphate dilithium salt is a solid, crystalline substance with a white color and no discernible odor. Being a zwitterionic compound, it contains both positive and negative charges. This compound finds utility as a substrate in enzyme assays, a buffer in electrophoresis, and an intermediate in the synthesis of various compounds. Additionally, it plays a role in the examination of enzyme kinetics.
Dihydroxyacetone phosphate dilithium salt (CAS 102783-56-2) References
- Quantification of intracellular phosphorylated carbohydrates in HT29 human colon adenocarcinoma cell line using liquid chromatography-electrospray ionization tandem mass spectrometry. | Vizán, P., et al. 2007. Anal Chem. 79: 5000-5. PMID: 17523595
- Novel (2R,3R)-2,3-butanediol dehydrogenase from potential industrial strain Paenibacillus polymyxa ATCC 12321. | Yu, B., et al. 2011. Appl Environ Microbiol. 77: 4230-3. PMID: 21531839
- In vitro glycation of human serum albumin by dihydroxyacetone and dihydroxyacetone phosphate. | Seneviratne, C., et al. 2012. Biochem Biophys Res Commun. 417: 817-23. PMID: 22198436
- Inclusion bodies of fuculose-1-phosphate aldolase as stable and reusable biocatalysts. | Sans, C., et al. 2012. Biotechnol Prog. 28: 421-7. PMID: 22275283
- Active site loop dynamics of a class IIa fructose 1,6-bisphosphate aldolase from Mycobacterium tuberculosis. | Pegan, SD., et al. 2013. Biochemistry. 52: 912-25. PMID: 23298222
- A noncompetitive inhibitor for Mycobacterium tuberculosis's class IIa fructose 1,6-bisphosphate aldolase. | Capodagli, GC., et al. 2014. Biochemistry. 53: 202-13. PMID: 24325645
- Sulphoglycolysis in Escherichia coli K-12 closes a gap in the biogeochemical sulphur cycle. | Denger, K., et al. 2014. Nature. 507: 114-7. PMID: 24463506
- Characterization of triosephosphate isomerase from Mycoplasma gallisepticum. | Bao, S., et al. 2015. FEMS Microbiol Lett. 362: fnv140. PMID: 26319024
- Highly efficient solid-phase derivatization of sugar phosphates with titanium-immobilized hydrophilic polydopamine-coated silica. | Qin, Q., et al. 2016. J Chromatogr A. 1457: 125-33. PMID: 27371021
- Effect of chronic exposure to monocrotophos on white adipose tissue in rats and its association with metabolic dyshomeostasis. | Nagaraju, R., et al. 2020. Hum Exp Toxicol. 39: 1190-1199. PMID: 32207356
- Deregulation of hepatic lipid metabolism associated with insulin resistance in rats subjected to chronic monocrotophos exposure. | Nagaraju, R., et al. 2020. J Biochem Mol Toxicol. 34: e22506. PMID: 32267039
- O-GlcNAc modification of leucyl-tRNA synthetase 1 integrates leucine and glucose availability to regulate mTORC1 and the metabolic fate of leucine. | Kim, K., et al. 2022. Nat Commun. 13: 2904. PMID: 35614056
- Chiral analysis of glycerol phosphates - can bacteria biosynthesize heterochiral phospholipid membranes? | Palyzová, A., et al. 2022. J Chromatogr A. 1676: 463267. PMID: 35767906
Substrate of:
Enzyme.Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Dihydroxyacetone phosphate dilithium salt, 5 mg | sc-214896 | 5 mg | $110.00 | |||
Dihydroxyacetone phosphate dilithium salt, 25 mg | sc-214896A | 25 mg | $280.00 |