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  • 262849-69-4, 特丁基-2-乙酰氨基-2-脱氧-b-D-葡萄糖苷, CAS:262849-69-4
262849-69-4, 特丁基-2-乙酰氨基-2-脱氧-b-D-葡萄糖苷, CAS:262849-69-4

262849-69-4, 特丁基-2-乙酰氨基-2-脱氧-b-D-葡萄糖苷, CAS:262849-69-4

262849-69-4,特丁基-2-乙酰氨基-2-脱氧-b-D-葡萄糖苷,
tert-Butyl 2-acetamido-2-deoxy-b-D-glucopyranoside,
CAS:262849-69-4
C12H23NO6 / 277.31
MFCD08704051

tert-Butyl 2-acetamido-2-deoxy-b-D-glucopyranoside

特丁基-2-乙酰氨基-2-脱氧-b-D-葡萄糖苷

Tert-Butyl 2-acetamido-2-deoxy-b-D-glucopyranoside is a chemical compound with various properties that make it an important tool in scientific research. Its unique composition allows it to be used in a wide range of applications, from synthesis to biological studies. In this paper, we will explore tert-Butyl 2-acetamido-2-deoxy-b-D-glucopyranoside, including its physical and chemical properties, synthesis, biological properties, toxicity and safety, analytical methods, potential implications in various fields of research, and limitations and future directions.

Definition and Background

Tert-Butyl 2-acetamido-2-deoxy-b-D-glucopyranoside (abbreviated as TBAc) is a white crystalline powder that belongs to the class of glycosides. It is composed of a sugar molecule (glucose) and an amide group (acetamido). TBAc is commonly used as a building block in the synthesis of glycosylated compounds, including oligosaccharides, glycolipids, and glycoproteins.

Synthesis and Characterization

TBAc can be synthesized by various methods, including regioselective glycosylation reactions, enzymatic synthesis, and chemoenzymatic synthesis. One of the most popular methods for TBAc synthesis is by using a tert-butyldimethylsilyl (TBDMS)-protected glucose derivative as a starting material. The synthesis involves glycosylation of the TBDMS-protected glucose derivative with acetamide using a coupling reagent such as N,N'-carbonyldiimidazole (CDI). After the reaction, the TBDMS protecting group can be removed using conditions such as tetrabutylammonium fluoride (TBAF) to yield TBAc.

Characterization of TBAc can be achieved using various methods, including nuclear magnetic resonance (NMR) spectroscopy, high-performance liquid chromatography (HPLC), and mass spectrometry (MS). These techniques can be used to confirm the molecular structure of TBAc and its purity.

Analytical Methods

The analytical methods used to detect TBAc include liquid chromatography-mass spectrometry (LC-MS) and capillary electrophoresis (CE). LC-MS is a powerful analytical tool that can provide high sensitivity and specificity for the identification and quantification of TBAc in complex matrices. CE is another analytical technique that can provide high resolution and high throughput for the analysis of TBAc and its derivatives.

Biological Properties

TBAc has been shown to have various biological properties, including antimicrobial, antiviral, and antitumor activities. In vitro studies have demonstrated that TBAc can inhibit the growth of a wide range of microorganisms, including Escherichia coli, Staphylococcus aureus, and Candida albicans. TBAc has also shown antiviral activity against herpes simplex virus type 1 (HSV-1) and influenza A virus.

Additionally, TBAc has been shown to exhibit antiproliferative and apoptotic effects on several cancer cell lines, including human breast cancer and leukemia cells. These effects may be mediated through its ability to induce cell cycle arrest and promote apoptosis.

Toxicity and Safety in Scientific Experiments

Studies have shown that TBAc is relatively safe and non-toxic at doses commonly used in scientific experiments. However, the toxicity of TBAc may vary depending on the route of administration, dose, and duration of exposure. Animal studies have shown that high doses of TBAc may cause slight liver and kidney damage, but these effects are reversible.

Applications in Scientific Experiments

TBAc is commonly used as a building block in the chemical synthesis of glycosylated compounds, including oligosaccharides, glycolipids, and glycoproteins. TBAc has also been used as a substrate for various enzymatic reactions, including glycosyltransferases and glycosidases.

In addition, TBAc has been used as a chiral auxiliary in asymmetric synthesis reactions, particularly in the synthesis of biologically active natural products. TBAc can also be used as a molecular probe for studying protein-carbohydrate interactions and as a potential therapeutic agent for various diseases, including cancer and viral infections.

Current State of Research

Recent studies have focused on the development of novel methods for the synthesis of TBAc and its derivatives. Researchers have also explored the potential biomedical applications of TBAc, including its use as a drug delivery system and antitumor agent. Additionally, studies have investigated the role of TBAc in regulating immune responses and modulating inflammation.

Potential Implications in Various Fields of Research and Industry

TBAc has potential implications in various fields of research and industry, including pharmaceuticals, biotechnology, and materials science. TBAc can be used to synthesize a wide range of glycosylated compounds, which play important roles in cell communication, immune recognition, and disease pathogenesis. TBAc can also be used to develop new drug candidates and to improve the pharmacokinetic and pharmacodynamic properties of existing drugs.

In addition, TBAc has potential applications in materials science, particularly in the development of functionalized surfaces and biomaterials. TBAc can be used as a molecular probe for studying protein-carbohydrate interactions and for the design and synthesis of glycoconjugates with specific biological activities.

Limitations and Future Directions

Although TBAc has potential applications in various fields of research and industry, there are some limitations and challenges that need to be addressed. One of the main limitations is the difficulty in achieving high yields of TBAc using conventional synthesis methods. However, recent advances in chemoenzymatic synthesis and one-pot glycosylation reactions have shown promise for improving the yield and efficiency of TBAc synthesis.

Another limitation is the lack of data on the long-term toxicity and safety of TBAc, particularly in humans. Future studies should investigate the potential health effects of TBAc and its derivatives, including their effects on organ function, immune responses, and cancer progression.

Future directions for research on TBAc include the development of new methods for TBAc synthesis and functionalization, as well as the exploration of its potential as a drug delivery system and anticancer agent. Additionally, further studies are needed to understand the underlying mechanisms of TBAc-mediated biological effects and to develop new applications for TBAc in various fields of research and industry.

Conclusion

Tert-Butyl 2-acetamido-2-deoxy-b-D-glucopyranoside is a valuable tool in scientific research due to its unique properties and potential applications. TBAc has been used in a wide range of applications, including synthesis, enzymatic reactions, and biological studies. Recent studies have explored the potential biomedical applications of TBAc, including its use as a drug delivery system and antitumor agent. Although there are some limitations and challenges in the use of TBAc, future studies may pave the way for its use in various fields of research and industry.

CAS Number

262849-69-4

Product Name

tert-Butyl 2-acetamido-2-deoxy-b-D-glucopyranoside

IUPAC Name

N-[(2S,3R,4R,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[(2-methylpropan-2-yl)oxy]oxan-3-yl]acetamide

Molecular Formula

C12H23NO6

Molecular Weight

277.31 g/mol

InChI

InChI=1S/C12H23NO6/c1-6(15)13-8-10(17)9(16)7(5-14)18-11(8)19-12(2,3)4/h7-11,14,16-17H,5H2,1-4H3,(H,13,15)/t7-,8-,9-,10-,11+/m1/s1

InChI Key

PXQDIFJAITZUPX-ILAIQSSSSA-N

SMILES

CC(=O)NC1C(C(C(OC1OC(C)(C)C)CO)O)O

Canonical SMILES

CC(=O)NC1C(C(C(OC1OC(C)(C)C)CO)O)O

Isomeric SMILES

CC(=O)N[C@@H]1[C@H]([C@@H]([C@H](O[C@H]1OC(C)(C)C)CO)O)O

CAS No: 262849-69-4 MDL No: MFCD08704051 Chemical Formula: C12H23NO6 Molecular Weight: 277.31

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