84635-54-1 , Methyl 2,3,4-tri-O-acetyl-b-L-thiofucopyranoside,
甲基-2,3,4-O-三乙酰基-b-L-硫代岩藻糖苷,
CAS:84635-54-1
C13H20O7S / 320.36
MFCD00080803
甲基-2,3,4-O-三乙酰基-b-L-硫代岩藻糖苷,
Methyl 2,3,4-tri-O-acetyl-b-L-thiofucopyranoside is a ferrite that is important for the growth of cells. It can be used as a growth factor to promote the growth of cells. Covid®-19 pandemic A/Aureus strain is resistant to this drug and it has been shown to inhibit cellular transformation in human epidermal cells. The drug also reduces the size and number of cancerous lesions in mice by inhibiting tumor angiogenesis. Methyl 2,3,4-tri-O-acetyl-b-L-thiofucopyranoside can cause an overload of Ca2+ ions in the cell, which may lead to apoptosis or necrosis.
Methyl TF is a fucose-containing disaccharide that has been widely used in the synthesis of oligosaccharides and glycoconjugates. It is an important building block for the construction of complex carbohydrates and has become a valuable synthetic tool in the study of carbohydrates.
Synthesis and Characterization:
Methyl TF can be synthesized by reacting 2,3,4-tri-O-acetyl-1-thio-L-fucopyranose with methyl iodide in the presence of a base. The compound can be characterized by various analytical techniques such as NMR spectroscopy, mass spectrometry, and X-ray crystallography.
Analytical Methods:
NMR spectroscopy is the most commonly used analytical technique for the characterization of Methyl TF. The technique provides detailed structural information of the compound, including its configuration and conformation. Other analytical techniques such as mass spectrometry and X-ray crystallography can also be used for the analysis of Methyl TF.
Biological Properties:
Methyl TF has been shown to exhibit biological activity, especially in the field of immunology. It has been found to modulate the immune response by enhancing the production of cytokines and stimulating the activation of T cells.
Toxicity and Safety in Scientific Experiments:
There is limited information available on the toxicity and safety of Methyl TF in scientific experiments. However, the compound should be handled with care as it may cause skin and eye irritation upon contact.
Applications in Scientific Experiments:
Methyl TF has found widespread application in the synthesis of oligosaccharides and glycoconjugates. It has been used in the synthesis of various complex carbohydrates, including the synthesis of the bacterial cell wall polysaccharide, alginate. Methyl TF has also been used in the development of carbohydrate-based vaccines.
Current State of Research:
Research on Methyl TF is ongoing, with a focus on the synthesis of complex carbohydrates and the development of glycoconjugate vaccines. There is a growing interest in the use of Methyl TF in the treatment of cancer and autoimmune diseases.
Potential Implications in Various Fields of Research and Industry:
Methyl TF has potential implications in various fields of research and industry, including immunology, drug discovery, and carbohydrate-based vaccine development. The compound could also find applications in the development of diagnostics for various diseases.
Limitations and Future Directions:
One limitation of Methyl TF is its limited solubility in water, which may hinder its application in certain scientific experiments. Future directions for research on Methyl TF include the exploration of its potential as a therapeutic agent for the treatment of cancer and autoimmune diseases. Other future directions include the development of new synthetic methods for the synthesis of complex carbohydrates and the development of glycoconjugate vaccines.
Conclusion:
Methyl TF is an important chemical compound in the study of carbohydrates, with potential implications in various fields of research and industry. The compound exhibits biological activity and has found widespread application in the synthesis of complex carbohydrates and the development of glycoconjugate vaccines. Future research on Methyl TF could lead to the development of new therapeutic agents for the treatment of cancer and autoimmune diseases.
CAS Number | 84635-54-1 |
Product Name | Methyl 2,3,4-Tri-O-acetyl-1-thio-beta-L-fucopyranoside |
IUPAC Name | [(2S,3R,4R,5S,6R)-4,5-diacetyloxy-2-methyl-6-methylsulfanyloxan-3-yl] acetate |
Molecular Formula | C13H20O7S |
Molecular Weight | 320.36 g/mol |
InChI | InChI=1S/C13H20O7S/c1-6-10(18-7(2)14)11(19-8(3)15)12(20-9(4)16)13(17-6)21-5/h6,10-13H,1-5H3/t6-,10+,11+,12-,13+/m0/s1 |
InChI Key | JOLBZRHXWOHZNS-MCNNAKBESA-N |
SMILES | CC1C(C(C(C(O1)SC)OC(=O)C)OC(=O)C)OC(=O)C |
Canonical SMILES | CC1C(C(C(C(O1)SC)OC(=O)C)OC(=O)C)OC(=O)C |
Isomeric SMILES | C[C@H]1[C@H]([C@H]([C@@H]([C@H](O1)SC)OC(=O)C)OC(=O)C)OC(=O)C |
CAS No: 84635-54-1 MDL No: MFCD00080803 Chemical Formula: C13H20O7S Molecular Weight: 320.36 |
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