Date published: 2026-6-6

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D-Lyxosylamine (CAS 39840-37-4)

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CAS Number:
39840-37-4
Molecular Weight:
149.15
Molecular Formula:
C5H11NO4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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D-Lyxosylamine, a derivative of D-lyxose, has garnered attention in scientific research due to its potential applications in carbohydrate chemistry and glycobiology. Its mechanism of action primarily revolves around its role as a precursor for synthesizing structurally diverse carbohydrate derivatives. Chemists utilize D-lyxosylamine as a building block in the synthesis of glycosides, glycoconjugates, and glycomimetics. Through various chemical transformations, such as glycosylation reactions and derivatization strategies, D-lyxosylamine enables the creation of novel carbohydrate-based compounds with tailored structures and functionalities. Moreover, researchers explore its use in studying carbohydrate-mediated biological processes, including glycan-protein interactions, cell surface recognition, and carbohydrate metabolism. By incorporating D-lyxosylamine into synthetic pathways, scientists aim to explain the roles of specific carbohydrates in biological systems and develop new tools for probing glycobiological phenomena. Furthermore, D-lyxosylamine serves as a valuable tool for probing enzyme mechanisms and inhibitor design in glycoscience research. Overall, D-Lyxosylamine plays a crucial role in advancing our understanding of carbohydrates′ functions and their applications in diverse fields, ranging from chemical biology to biomaterials science.


D-Lyxosylamine (CAS 39840-37-4) References

  1. In the search for new anticancer drugs. XXIII: Exploration of a predictive design for anticancer drugs of carbohydrates containing N-nitrosochloroethylamino, N-nitrosomethyl, and N-nitrosoaminoxyl components.  |  Sosnovsky, G. and Rao, NU. 1991. J Pharm Sci. 80: 693-9. PMID: 1658297
  2. Composition of Herba Pogostemonis water extract and protection of infected mice against Salmonella Typhimurium-induced liver damage and mortality by stimulation of innate immune cells.  |  Kim, SP., et al. 2012. J Agric Food Chem. 60: 12122-30. PMID: 23186318
  3. Enzyme immunoassay for macrolide antibiotics: characterization of an antibody to 23-amino-O-mycaminosyltylonolide.  |  Yao, RC. and Mahoney, DF. 1989. Appl Environ Microbiol. 55: 1507-11. PMID: 2764563
  4. Untargeted Metabolomics Insights into Newborns with Congenital Zika Infection.  |  Nunes, EDC., et al. 2021. Pathogens. 10: PMID: 33924291
  5. Spatioregional assessment of the gut microbiota in experimental necrotizing pancreatitis.  |  van den Berg, FF., et al. 2021. BJS Open. 5: PMID: 34518874
  6. Carbohydrate-binding specificities and physico-chemical properties of lectins in various tissue of phlebotominae sandflies.  |  Palánová, L. and Volf, P. 1997. Folia Parasitol (Praha). 44: 71-6. PMID: 9188176
  7. Second-order nonlinear optical properties of saccharide materials[C]  |  Bourhill G, Mansour K, Perry K J,. 1993,. Organic and Biological Optoelectronics. SPIE,. 1853: 110-125.
  8. Chemical properties investigation of commercial cigarettes by a "pseudo" targeted method using GC‐MS‐selected ions monitoring[J].  |  Li Y, Pang T, Li Y. 2013,. Journal of separation science,. 36(9-10): 1545-1552.
  9. Metabolomic basis of laboratory evolution of butanol tolerance in photosynthetic Synechocystis sp. PCC 6803[J].  |  Wang Y, Shi M, Niu X,. 2014. Microbial Cell Factories,. 13: 1-12.
  10. Assessment of shade-unshade condition and subsequently pesticide treatment on first flush tea leaf metabolites through GC/MS based metabolomics approach[J].  |  Ray S, Chatterjee J, Ghosh A. 2021. Cogent Food & Agriculture,. 7(1): 1930424.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

D-Lyxosylamine, 5 g

sc-221497
5 g
$380.00