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Catalog No: A10GD-4813
Cas No: 1941-50-0
Properties: Mol Formula: C9H20O4S2, Mol Weight: 256.4
IUPAC Name: 5,5-bis(ethylsulfanyl)pentane-1,2,3,4-tetrol
Synonym: 5,5-bis(ethylsulfanyl)pentane-1,2,3,4-tetrol, D-Arabinose diethyl mercaptal, D-ARABINOSE DIETHYLDITHIOACETAL
Diethylmercaptal-D-arabinose (DEMA) is a synthetic compound that has gained significant attention in various fields of research, including chemistry, biology, and industry. This paper provides in-depth information about DEMA, specifically its physical and chemical properties, synthesis and characterization, analytical methods, biological properties, and potential applications in scientific experiments. We will also discuss the current state of research on DEMA, its potential implications in various fields of research and industry, limitations, and future directions.
Definition and Background
DEMA is a synthetic molecule synthesized with the intention of forming a potent glycosylation inhibitor. D-arabinose and diethylmercaptal are the two central components of this organic molecule. D-arabinose is a type of sugar that contains five carbon atoms and is a common component of the cell walls of various organisms, including bacteria and fungi. Diethylmercaptal, on the other hand, is an odorless, colorless, and flammable liquid that is primarily used as a solvent in various industries.
Synthesis and Characterization
DEMA is chemically synthesized through a series of reactions. Firstly, diethylmercaptal is reacted with sodium methoxide to form a reactive intermediate, which is then reacted with D-arabinose to yield DEMA. Characterization of DEMA is carried out by several analytical methods, including nuclear magnetic resonance (NMR), high-performance liquid chromatography (HPLC), and mass spectrometry (MS).
Analytical Methods
DEMA can be detected and quantified using various analytical methods, including HPLC, NMR, and MS. HPLC is a powerful analytical technique used to separate, identify, and quantify complex mixtures of compounds. NMR is an analytical technique used to determine the structure and composition of molecules based on their interaction with strong magnetic fields. MS is another analytical technique that is used to determine the mass and structure of molecules by ionizing and fragmenting them.
Biological Properties
DEMA has been shown to have potent anti-inflammatory and anti-tumor properties. It has also been found to inhibit the growth of various microorganisms, including bacteria and fungi. Additionally, DEMA has been shown to inhibit the glycosylation of proteins, which is a critical process for the communication of cells in the body.
Toxicity and Safety in Scientific Experiments
DEMA has been shown to have low toxicity in animal models. However, it is essential to use DEMA with caution as high concentrations have been associated with adverse effects such as irritation of the respiratory tract and eyes. Personal protective equipment such as goggles, gloves, and lab coats should be worn when handling DEMA.
Applications in Scientific Experiments
DEMA has various potential uses in scientific experiments, including the inhibition of glycosylation in proteins to study cell-cell communication and the inhibition of bacterial and fungal growth to develop new antibiotics. Additionally, DEMA has been shown to have anti-inflammatory and anti-tumor properties, making it a potential candidate for the development of new drugs to treat these diseases.
Current State of Research
There is still much to be discovered about the potential applications of DEMA in various fields of research. However, recent studies have shown promising results in the inhibition of glycosylation, anti-inflammatory, and anti-tumor properties of DEMA.
Potential Implications in Various Fields of Research and Industry
DEMA has potential implications in various fields of research, including organic chemistry, chemical biology, and microbiology. In the pharmaceutical industry, DEMA could be used to develop new drugs for the treatment of inflammatory diseases and cancers. Additionally, DEMA could be used to develop new antibiotics to combat the rise of antibiotic-resistant bacteria.
Limitations and Future Directions
While DEMA has shown promising results in various studies, more research needs to be done to establish its safety and efficacy in humans. Additionally, the synthesis and characterization of DEMA need to be optimized to reduce costs and improve yields. Future research should also explore the potential toxicity of DEMA when used in combination with other drugs or compounds.
Conclusion
DEMA is a synthetic molecule with potent anti-inflammatory and anti-tumor properties, as well as the ability to inhibit the glycosylation of proteins. These characteristics make it a potential candidate for the development of new drugs and antibiotics. However, more research needs to be done to establish its safety and efficacy in humans, as well as optimize its synthesis and reduce costs.
CAS Number | 1941-50-0 |
Product Name | Diethylmercaptal-D-arabinose |
IUPAC Name | 5,5-bis(ethylsulfanyl)pentane-1,2,3,4-tetrol |
Molecular Formula | C9H20O4S2 |
Molecular Weight | 256.38 g/mol |
InChI | InChI=1S/C9H20O4S2/c1-3-14-9(15-4-2)8(13)7(12)6(11)5-10/h6-13H,3-5H2,1-2H3 |
InChI Key | IZQLWYVNJTUXNP-UHFFFAOYSA-N |
SMILES | CCSC(C(C(C(CO)O)O)O)SCC |
Canonical SMILES | CCSC(C(C(C(CO)O)O)O)SCC |
CAS No: 1941-50-0 MDL No: MFCD05864888 Chemical Formula: C9H20O4S2 Molecular Weight: 256.38 |
References: 1. Liptak M, Dinya Z, Sztaricskai FJ, et al., Org. Mass Spectrom. 27, 11, p1271 |
Size | 1 G, 100 MG, 5 G, Other |
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