Molecular structure of Lithium β-hydroxypyruvate, CAS Number: 3369-79-7
Lithium β-hydroxypyruvate (CAS 3369-79-7)
Alternate Names:
hydroxypyruvic acid
Application:
Lithium β-hydroxypyruvate is a substrate for transketolase
CAS Number:
3369-79-7
Purity:
>97%
Molecular Weight:
109.99
Molecular Formula:
C3H3LiO4
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
Lithium β-hydroxypyruvate is a substrate for transketolase, and used for the production of optically pure L-2-hydroxy aldehydes.
Lithium β-hydroxypyruvate (CAS 3369-79-7) References
- Enzymatic and mechanistic studies on the formation of N-phenylglycolohydroxamic acid from nitrosobenzene and pyruvate in spinach leaf homogenate. | Tatsunami, R. and Yoshioka, T. 2006. J Agric Food Chem. 54: 590-6. PMID: 16417326
- Purification and characterization of hydroxypyruvate reductase from the facultative methylotroph Methylobacterium extorquens AM1. | Chistoserdova, LV. and Lidstrom, ME. 1991. J Bacteriol. 173: 7228-32. PMID: 1657886
- Purification and characterization of hydroxypyruvate reductase from a serine-producing methylotroph, Hyphomicrobium methylovorum GM2. | Izumi, Y., et al. 1990. Eur J Biochem. 190: 279-84. PMID: 2114287
- Identification of catalytically important amino acid residues for enzymatic reduction of glyoxylate in plants. | Hoover, GJ., et al. 2013. Biochim Biophys Acta. 1834: 2663-71. PMID: 24076009
- An efficient amperometric transketolase assay: towards inhibitor screening. | Touisni, N., et al. 2014. Biosens Bioelectron. 62: 90-6. PMID: 24984289
- Real-time pH monitoring of industrially relevant enzymatic reactions in a microfluidic side-entry reactor (μSER) shows potential for pH control. | Gruber, P., et al. 2017. Biotechnol J. 12: PMID: 28106351
- Enzymatic synthesis of chiral amino-alcohols by coupling transketolase and transaminase-catalyzed reactions in a cascading continuous-flow microreactor system. | Gruber, P., et al. 2018. Biotechnol Bioeng. 115: 586-596. PMID: 28986983
- A catechol oxidase AcPPO from cherimoya (Annona cherimola Mill.) is localized to the Golgi apparatus. | Olmedo, P., et al. 2018. Plant Sci. 266: 46-54. PMID: 29241566
- One-pot, two-step transaminase and transketolase synthesis of l-gluco-heptulose from l-arabinose. | Bawn, M., et al. 2018. Enzyme Microb Technol. 116: 16-22. PMID: 29887012
- Substrate specificity and carbohydrate synthesis using transketolase | Yoshihiro Kobori, David C. Myles, and George M. Whitesides. 1992. J. Org. Chem. 58: 5899-5907.
- Preparation of optically pure L-2-hydroxyaldehydes with yeast transketolase | Franz Effenberger ∗, Volker Null, Thomas Ziegler. 1992. Tetrahedron Letters. 33: 5157-5160.
- Chiral polyol synthesis catalyzed by a thermostable Transketolase immobilized on Layered Double Hydroxides in Ionic liquids | Dr. Ghina Ali, Dr. Thomas Moreau, Prof. Claude Forano, Dr. Christine Mousty, Dr. Vanessa Prevot, Dr. Franck Charmantray, Prof. Laurence Hecquet. 2015. ChemCatChem. 7: 3163-3170.
- Transketolase catalysed upgrading of L-arabinose: the one-step stereoselective synthesis of L-gluco-heptulose | Fabiana Subrizi a, Max Cárdenas-Fernández b, Gary J. Lye b, John M. Ward b, Paul A. Dalby b, Tom D. Sheppard a and Helen C. Hailes *a. 2016. Green chemistry. 18: 3158-3165.
Substrate of:
Transketolase.Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Lithium β-hydroxypyruvate, 1 g | sc-252955 | 1 g | $292.00 |