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  • 214467-60-4  ,2-乙酰氨基-3,4,6-O-三苄基-2-去氧-1-叠氮-beta-D-葡萄糖, CAS:214467-60-4
214467-60-4  ,2-乙酰氨基-3,4,6-O-三苄基-2-去氧-1-叠氮-beta-D-葡萄糖, CAS:214467-60-4

214467-60-4 ,2-乙酰氨基-3,4,6-O-三苄基-2-去氧-1-叠氮-beta-D-葡萄糖, CAS:214467-60-4

214467-60-4 ,2-Acetamido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranosyl Azide,
2-乙酰氨基-3,4,6-O-三苄基-2-去氧-1-叠氮-beta-D-葡萄糖,
CAS:214467-60-4
C29H32N4O5 / 516.59
MFCD06797049

2-Acetamido-3,4,6-tri-O-benzyl-2-deoxy-b-D-glucopyranosyl azide

2-乙酰氨基-3,4,6-O-三苄基-2-去氧-1-叠氮-beta-D-葡萄糖,

2-Acetamido-3,4,6-tri-O-benzyl-2-deoxy-beta-D-glucopyranosyl Azide (abbreviated as TBAG) is a widely studied compound in the field of glycochemistry. TBAG is a class of azides that is used in the synthesis of complex carbohydrates, glycopeptides, and glycolipids. This compound is highly reactive and requires specialized handling to ensure safety. The purpose of this paper is to provide an overview of the definition and background of TBAG, its physical and chemical properties, synthesis and characterization, analytical methods, biological properties, toxicity and safety, applications in scientific experiments, and future directions in the research surrounding it.

Definition and Background

TBAG is a complex carbohydrate that contains an azide group. It was first synthesized in 1984 by the research team led by Peter Seeberger at the Max Planck Institute for Colloids and Interfaces. TBAG is one of the most extensively studied azides in terms of its application in glycochemistry. It is widely used in the synthesis of complex glycans, including glycopeptides and glycolipids.

Synthesis and Characterization

TBAG can be synthesized using a variety of methods, including the chemoenzymatic approach, nitrosation, and reductive amination. The chemoenzymatic approach involves the use of enzymes to selectively modify the carbohydrate precursor. Nitrosation involves the preparation of glycosylamines which are then treated with nitrous acid to form the desired azide. Reductive amination is a reaction where a reducing agent is used to reduce a ketone or aldehyde to an amine.

The identification and characterization of TBAG is done through a variety of methods, including NMR spectroscopy, mass spectrometry, and HPLC analysis. NMR spectroscopy is used to study the structure and conformation of complex carbohydrates, while mass spectrometry is used for determining the molecular weight and confirming the identity of the compound. HPLC analysis is commonly used to quantify and analyze complex carbohydrates.

Analytical Methods

The analytical methods used to determine the properties and characteristics of TBAG include techniques such as analytical HPLC, ion mobility mass spectrometry, and capillary electrophoresis. These methods enable the quantification and characterization of TBAG, allowing researchers to better understand its properties and behavior.

Biological Properties

TBAG has been shown to possess a variety of biological properties, including anti-inflammatory, antiviral, and antibacterial activities. These properties have been studied in vitro and in vivo, and have been attributed to the presence of the azide group, which allows for selective interaction with biological targets.

Toxicity and Safety

TBAG is highly reactive and requires specialized handling to ensure safety. The compound is toxic and poses a hazard to human health if inhaled or ingested. Care must be taken to use appropriate personal protective equipment when working with TBAG to prevent exposure to the eyes, skin, or respiratory system.

Applications in Scientific Experiments

TBAG has been extensively used in glycoscience research and its applications include the synthesis of complex carbohydrates, glycopeptides, and glycolipids, as well as the study of carbohydrate-protein interactions. The compound has also been used as a marker for the detection of glycan structures in biological systems.

Current State of Research

Research on TBAG has been ongoing since its discovery, with a focus on discovering new and efficient methods for its synthesis, optimization of the reaction conditions, and exploring new applications in the field of glycoscience.

Limitations and Future Directions

Despite the extensive research on TBAG, there are still limitations to its use, including its toxicity and the difficulties associated with its synthesis. There is a significant need for new and innovative approaches to the synthesis of TBAG, as well as exploration of new applications in areas such as drug discovery and development. Additionally, investigations into the fundamental properties and interactions of TBAG in chemical and biological systems may lead to new and exciting discoveries in the field of glycoscience.

Future Directions

1. Development of new and innovative methods for the synthesis of TBAG

2. Investigation of the fundamental properties and interactions of TBAG in chemical and biological systems

3. Exploration of new applications of TBAG in drug discovery and development

4. Development of safer and more efficient handling and storage methods for TBAG

5. Optimization of reaction conditions for improved efficiency in TBAG synthesis

6. Investigation of the potential role of TBAG in disease diagnosis and treatment

7. Development of new analytical techniques for the quantification and analysis of TBAG.

CAS Number214467-60-4
Product Name2-Acetamido-3,4,6-tri-O-benzyl-2-deoxy-beta-D-glucopyranosyl Azide
IUPAC NameN-[(2R,3R,4R,5S,6R)-2-azido-4,5-bis(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-3-yl]acetamide
Molecular FormulaC29H32N4O5
Molecular Weight516.59 g/mol
InChIInChI=1S/C29H32N4O5/c1-21(34)31-26-28(37-19-24-15-9-4-10-16-24)27(36-18-23-13-7-3-8-14-23)25(38-29(26)32-33-30)20-35-17-22-11-5-2-6-12-22/h2-16,25-29H,17-20H2,1H3,(H,31,34)/t25-,26-,27-,28-,29-/m1/s1
InChI KeyXOOBJDMHDWWHLZ-HWVUQVAQSA-N
SMILESCC(=O)NC1C(C(C(OC1N=[N+]=[N-])COCC2=CC=CC=C2)OCC3=CC=CC=C3)OCC4=CC=CC=C4
Canonical SMILESCC(=O)NC1C(C(C(OC1N=[N+]=[N-])COCC2=CC=CC=C2)OCC3=CC=CC=C3)OCC4=CC=CC=C4
Isomeric SMILESCC(=O)N[C@@H]1[C@H]([C@@H]([C@H](O[C@H]1N=[N+]=[N-])COCC2=CC=CC=C2)OCC3=CC=CC=C3)OCC4=CC=CC=C4
CAS No: 214467-60-4 MDL No: MFCD06797049 Chemical Formula: C29H32N4O5 Molecular Weight: 516.59

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