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  • 54322-38-2 ,4-甲基伞形酮-alpha-L-吡喃岩藻糖苷, CAS:54322-38-2
54322-38-2 ,4-甲基伞形酮-alpha-L-吡喃岩藻糖苷, CAS:54322-38-2

54322-38-2 ,4-甲基伞形酮-alpha-L-吡喃岩藻糖苷, CAS:54322-38-2

54322-38-2,4-甲基伞形酮-alpha-L-吡喃岩藻糖苷,
4-Methylumbelliferyl a-L-fucopyranose,
CAS:54322-38-2
C16H18O7 / 322.31
MFCD00051218

4-Methylumbelliferyl a-L-fucopyranoside

4-甲基伞形酮-alpha-L-吡喃岩藻糖苷

4-Methylumbelliferyl-alpha-L-fucopyranoside is a fluorescent substrate that is commonly used in research to detect the presence of the enzyme alpha-L-fucosidase. Alpha-L-fucosidase is an enzyme that is responsible for the hydrolysis of fucose-containing compounds like glycoproteins and glycolipids. In this paper, we will discuss the definition and background, physical and chemical properties, synthesis, characterization, analytical methods, biological properties, toxicity and safety in scientific experiments, applications in scientific experiments, current state of research, potential implications in various fields of research and industry, limitations, and future directions of 4-Methylumbelliferyl-alpha-L-fucopyranoside.

Definition and Background:

4-Methylumbelliferyl-alpha-L-fucopyranoside is a substrate that is commonly used to detect alpha-L-fucosidase, an enzyme that is responsible for breaking down fucose-containing compounds like glycoproteins and glycolipids. Fucosylation is an important post-translational modification that plays a significant role in various biological processes like cell adhesion, signaling, and embryonic development. Defects in fucosylation have been linked to various diseases like cancer, inflammation, and developmental disorders.

Synthesis and Characterization:

The synthesis of 4-Methylumbelliferyl-alpha-L-fucopyranoside can be carried out through the reaction of 4-methylumbelliferone with alpha-L-fucopyranosyl fluoride in the presence of a Lewis acid catalyst like BF3-etherate. The reaction typically occurs under reflux conditions for several hours, and the product can be purified through column chromatography. The purity of the product can be confirmed through various analytical techniques like thin layer chromatography (TLC), high-performance liquid chromatography (HPLC), and NMR spectroscopy.

Analytical Methods:

4-Methylumbelliferyl-alpha-L-fucopyranoside can be detected using various analytical methods like fluorescence spectroscopy, HPLC, and TLC. Fluorescence spectroscopy is the most commonly used technique as it allows for the sensitive and selective detection of alpha-L-fucosidase activity. Upon hydrolysis by the enzyme, 4-Methylumbelliferyl-alpha-L-fucopyranoside produces a fluorescent compound, which can be detected using a fluorometer.

Biological Properties:

The biological properties of 4-Methylumbelliferyl-alpha-L-fucopyranoside are primarily related to its ability to act as a substrate for alpha-L-fucosidase. Alpha-L-fucosidase is an enzyme that is involved in the hydrolysis of fucose-containing compounds, which play important roles in various biological processes like cell adhesion, signaling, and embryonic development. The expression and activity of alpha-L-fucosidase have been linked to various diseases like cancer and inflammation.

Toxicity and Safety in Scientific Experiments:

4-Methylumbelliferyl-alpha-L-fucopyranoside is considered to be safe for use in scientific experiments. However, caution should be exercised when handling the compound as it may cause skin and eye irritation. It is recommended to wear gloves and safety goggles when handling the compound.

Applications in Scientific Experiments:

4-Methylumbelliferyl-alpha-L-fucopyranoside is commonly used to detect the presence of alpha-L-fucosidase in biological samples. It can be used in various scientific experiments to study the role of fucosylation and alpha-L-fucosidase in biological processes like cell adhesion, signaling, and embryonic development. It is also used in clinical diagnostics to detect the activity of alpha-L-fucosidase in patient samples.

Current State of Research:

Research on 4-Methylumbelliferyl-alpha-L-fucopyranoside has primarily focused on its use as a substrate for alpha-L-fucosidase detection. Recent studies have investigated the use of 4-Methylumbelliferyl-alpha-L-fucopyranoside in the detection of alpha-L-fucosidase activity in cancer cells and the analysis of fucosylation in patient samples.

Potential Implications in Various Fields of Research and Industry:

4-Methylumbelliferyl-alpha-L-fucopyranoside has potential implications in various fields of research and industry. It can be used in clinical diagnostics to detect the activity of alpha-L-fucosidase in patient samples, which can help in the diagnosis and monitoring of diseases like cancer and inflammation. It can also be used in the development of drugs targeting alpha-L-fucosidase activity.

Limitations and Future Directions:

One limitation of 4-Methylumbelliferyl-alpha-L-fucopyranoside is that it is specific to alpha-L-fucosidase detection and does not detect other fucose-containing compounds. Future research could focus on the development of substrates that can detect a broader range of fucose-containing compounds. Other future directions could include the investigation of the role of fucosylation and alpha-L-fucosidase in various disease states and the development of drugs targeting alpha-L-fucosidase activity.

Conclusion:

In conclusion, 4-Methylumbelliferyl-alpha-L-fucopyranoside is a valuable tool for the detection of alpha-L-fucosidase in various scientific experiments and clinical diagnostics. Its physical and chemical properties, synthesis, analytical methods, biological properties, toxicity and safety in scientific experiments, applications, current state of research, potential implications, limitations, and future directions have been discussed in this paper. Further research is necessary to fully understand the role of fucosylation and alpha-L-fucosidase in various biological processes and disease states.

CAS Number54322-38-2
Product Name4-Methylumbelliferyl-alpha-L-fucopyranoside
IUPAC Name4-methyl-7-[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-2-one
Molecular FormulaC16H18O7
Molecular Weight322.31 g/mol
InChIInChI=1S/C16H18O7/c1-7-5-12(17)23-11-6-9(3-4-10(7)11)22-16-15(20)14(19)13(18)8(2)21-16/h3-6,8,13-16,18-20H,1-2H3/t8-,13+,14+,15-,16-/m0/s1
InChI KeyCQKHENXHLAUMBH-CRLRYRHBSA-N
SMILESCC1C(C(C(C(O1)OC2=CC3=C(C=C2)C(=CC(=O)O3)C)O)O)O
Synonyms4-methylumbelliferyl fucoside, MUB-fucoside
Canonical SMILESCC1C(C(C(C(O1)OC2=CC3=C(C=C2)C(=CC(=O)O3)C)O)O)O
Isomeric SMILESC[C@H]1[C@H]([C@H]([C@@H]([C@@H](O1)OC2=CC3=C(C=C2)C(=CC(=O)O3)C)O)O)O
CAS No: 54322-38-2 Synonyms: 4-MU-a-L-Fuc MDL No: MFCD00051218 Chemical Formula: C16H18O7 Molecular Weight: 322.31

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