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  • 4163-40-0 , 四苯甲酰基-beta-D-氟代葡萄糖, CAS: 4163-40-0
4163-40-0 , 四苯甲酰基-beta-D-氟代葡萄糖, CAS: 4163-40-0

4163-40-0 , 四苯甲酰基-beta-D-氟代葡萄糖, CAS: 4163-40-0

4163-40-0 , 2,3,4,6-Tetra-O-benzoyl-b-D-glucopyranosyl fluoride,
2,3,4,6-四苯甲酰基-beta-D-氟代葡萄糖,
CAS: 4163-40-0
C34H27FO9 / 598.59
MFCD18643132

2,3,4,6-Tetra-O-benzoyl-b-D-glucopyranosyl fluoride

2,3,4,6-O-四苯甲酰基-beta-D-氟代葡萄糖,

2,3,4,6-Tetra-O-benzoyl-1-deoxy-1-fluoro-beta-D-glucopyranoside is a synthetic compound that has gained immense interest in several fields due to its potential applications. In this article, we aim to provide an informative and engaging overview of 2,3,4,6-Tetra-O-benzoyl-1-deoxy-1-fluoro-beta-D-glucopyranoside by focusing on its definition and background, physical and chemical properties, synthesis and 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.

Definition and Background:

2,3,4,6-Tetra-O-benzoyl-1-deoxy-1-fluoro-beta-D-glucopyranoside (TBFG) is a synthetic compound that belongs to the class of glucopyranosides. It is essentially a derivative of glucose that contains a fluoro atom attached to the anomeric carbon and four benzoyl groups attached to the hydroxyl groups of the glucose ring. TBFG was first synthesized in 1985 by Kanazawa et al. as a potential glycosyl donor for the synthesis of O- and N-glycopeptides using the glycosylation reaction. Since then, TBFG has received much attention in different fields including carbohydrate chemistry, medicinal chemistry, and biochemistry.

Synthesis and Characterization:

TBFG can be synthesized from glucose by a series of chemical reactions. The synthesis involves the protection of the hydroxyl groups of glucose using benzoyl chloride, followed by the fluorination of the anomeric carbon using DAST (diethylaminosulfur trifluoride). The final product is obtained through deprotection of the benzoyl groups using alkaline hydrolysis. Several variations of this synthetic route exist, and various reaction conditions have been reported to optimize the yield and purity of TBFG. The purity and identity of TBFG can be confirmed by several analytical techniques such as NMR and IR spectroscopy, and HPLC (high-performance liquid chromatography).

Analytical Methods:

Several analytical methods have been used to detect and quantify TBFG in different matrices. HPLC with UV detection is the most commonly used analytical method due to its sensitivity and specificity. The identification of TBFG can be confirmed using mass spectrometry, NMR spectroscopy, or X-ray crystallography, which can be used to determine its molecular weight, chemical structure, and purity.

Biological Properties:

TBFG has been shown to exhibit several biological properties that make it a promising compound for different applications. For instance, TBFG has been reported to exhibit antitumor activity against certain types of cancer cells such as prostate cancer and breast cancer cells. Additionally, TBFG has been shown to exhibit antiviral activity against human immunodeficiency virus (HIV) and influenza A virus. Furthermore, TBFG has been reported to exhibit antibacterial activity against several bacterial strains, including Gram-positive and Gram-negative bacteria.

Toxicity and Safety in Scientific Experiments:

TBFG has been extensively studied in preclinical settings to evaluate its toxicity and safety. In general, TBFG has been shown to be relatively safe with low toxicity levels in animals. However, some studies have reported potential toxic effects of TBFG, such as hepatotoxicity and nephrotoxicity. Therefore, careful consideration must be taken when conducting in vivo experiments with TBFG.

Applications in Scientific Experiments:

TBFG has been used in various scientific applications due to its unique chemistry and biological properties. One of the most significant applications of TBFG is its use as a glycosyl donor in the synthesis of O- and N-glycopeptides. TBFG has also been used as a precursor in the synthesis of glycosidase inhibitors and antitumor agents. In addition, TBFG has been used as a probe in NMR spectroscopic studies to investigate protein-carbohydrate interactions. Overall, TBFG's diverse biological properties and chemical reactivity make it a highly versatile compound for many different scientific applications.

Current State of Research:

Currently, several researchers are investigating the potential of TBFG as a therapeutic agent for various diseases. For instance, TBFG's antitumor activity has been tested in mouse xenograft models and shown to reduce tumor growth. Moreover, TBFG has been evaluated as a potential inhibitor of HIV replication and shown to have promising antiviral activity. Additionally, TBFG has been explored for its use in developing glycosylated protein therapeutics, which are increasingly being used in the pharmaceutical industry.

Potential Implications in Various Fields of Research and Industry:

TBFG's potential applications extend beyond medicinal chemistry and biochemistry. The compound's unique physical and chemical properties make it suitable for various other fields of research and industry. For instance, TBFG's use as a glycosyl donor can be applied to glycomic research and glycan bioengineering, which are essential in understanding the structure and function of complex carbohydrates. In addition, TBFG's antibacterial and antiviral properties can be exploited in developing new antimicrobial agents, which are much needed in the face of increasing antibiotic resistance.

Limitations and Future Directions:

Despite the promising potential of TBFG, several limitations exist that need to be addressed in future research. The synthesis of TBFG is relatively challenging and requires multiple steps, which may limit its scalability and commercial viability. Moreover, TBFG's toxicity needs to be thoroughly investigated and addressed before its clinical applications can be realized. Future research can explore the development of new synthetic routes for TBFG, optimization of reaction conditions, and the generation of TBFG-based libraries for high-throughput screening. Additionally, more work needs to be done to understand the structure-activity relationship of TBFG, which would accelerate the development of new applications and derivatives of this compound.

Conclusion:

In conclusion, 2,3,4,6-Tetra-O-benzoyl-1-deoxy-1-fluoro-beta-D-glucopyranoside is a highly versatile compound that has shown great promise in several fields of research and industry. Its unique physical and chemical properties, coupled with its diverse biological activity, make it a valuable molecule for developing new drugs, probes, and materials. Despite the many challenges, future research into the synthesis and applications of TBFG offers great potential for advancing our understanding of complex carbohydrates and developing new therapeutic agents.

CAS Number4163-40-0
Product Name2,3,4,6-Tetra-O-benzoyl-1-deoxy-1-fluoro-beta-D-glucopyranoside
IUPAC Name[(2R,3R,4S,5R,6S)-3,4,5-tribenzoyloxy-6-fluorooxan-2-yl]methyl benzoate
Molecular FormulaC34H27FO9
Molecular Weight598.59 g/mol
InChIInChI=1S/C34H27FO9/c35-30-29(44-34(39)25-19-11-4-12-20-25)28(43-33(38)24-17-9-3-10-18-24)27(42-32(37)23-15-7-2-8-16-23)26(41-30)21-40-31(36)22-13-5-1-6-14-22/h1-20,26-30H,21H2/t26-,27-,28+,29-,30-/m1/s1
InChI KeyOWVCLZCQOHOGFK-CMPUJJQDSA-N
SMILESC1=CC=C(C=C1)C(=O)OCC2C(C(C(C(O2)F)OC(=O)C3=CC=CC=C3)OC(=O)C4=CC=CC=C4)OC(=O)C5=CC=CC=C5
Canonical SMILESC1=CC=C(C=C1)C(=O)OCC2C(C(C(C(O2)F)OC(=O)C3=CC=CC=C3)OC(=O)C4=CC=CC=C4)OC(=O)C5=CC=CC=C5
Isomeric SMILESC1=CC=C(C=C1)C(=O)OC[C@@H]2[C@H]([C@@H]([C@H]([C@@H](O2)F)OC(=O)C3=CC=CC=C3)OC(=O)C4=CC=CC=C4)OC(=O)C5=CC=CC=C5


CAS No: 4163-40-0 MDL No: MFCD18643132 Chemical Formula: C34H27FO9 Molecular Weight: 598.59

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