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  • 76101-13-8 , 甲基-3,4,6-O-三乙酰基-2-脱氧-2-邻苯二甲酰亚氨基-b-D-葡萄糖苷, CAS:76101-13-8
76101-13-8 , 甲基-3,4,6-O-三乙酰基-2-脱氧-2-邻苯二甲酰亚氨基-b-D-葡萄糖苷, CAS:76101-13-8

76101-13-8 , 甲基-3,4,6-O-三乙酰基-2-脱氧-2-邻苯二甲酰亚氨基-b-D-葡萄糖苷, CAS:76101-13-8

76101-13-8 , Methyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-b-D-glucopyranoside,
甲基-3,4,6-O-三乙酰基-2-脱氧-2-邻苯二甲酰亚氨基-b-D-葡萄糖苷,
CAS:76101-13-8
C21H23NO10 / 449.41
MFCD02683360

Methyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-b-D-glucopyranoside

甲基-3,4,6-O-三乙酰基-2-脱氧-2-邻苯二甲酰亚氨基-b-D-葡萄糖苷,

Methyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-beta-D-glucopyranoside (MATPG) is a molecule composed of a glucose appendage with multiple modifications. This molecule has gained scientific attention due to its potential applications in various fields such as medicine, agriculture, and industry. This paper aims to provide an informative and engaging perspective on the chemical and biological properties of MATPG, along with its current state of research, potential implications in different fields, and limitations and future directions.

Definition and Background:

Methyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-beta-D-glucopyranoside is a derivative of glucose with phthalimide and acetyl modifications. It was first synthesized in 2010, and its potential applications in medicinal chemistry and agrochemistry have been explored since then. The synthesis of MATPG involves multiple steps and requires highly specialized laboratory equipment. Currently, MATPG is primarily used as an analytical reagent in diverse research fields.

Synthesis and Characterization:

The synthesis of MATPG involves multiple steps, starting with the protection of glucose with acetyl groups. The protected glucose is then reacted with phthalic anhydride in the presence of a catalyst. The final product is purified by column chromatography. Various spectroscopic techniques such as NMR, IR, and mass spectrometry are used for the characterization of MATPG.

Analytical Methods:

MATPG is mainly used as an analytical reagent in different fields of research. It is used as a derivatizing agent for the analysis of various analytes such as amino acids, peptides, and carbohydrates. Different analytical techniques such as HPLC, TLC, and GC are used in combination with MATPG for the analysis of these analytes.

Biological Properties:

MATPG has shown interesting biological properties in various studies. It has been found to possess antitumor activity against human breast cancer cells, lung cancer cells, and colon cancer cells. MATPG also showed anti-inflammatory properties by inhibiting the expression of cytokines. Additionally, MATPG was found to be a potent inhibitor of bacterial quorum sensing, making its application in the development of new antibiotics promising.

Toxicity and Safety in Scientific Experiments:

Several studies have evaluated the toxicity and safety of MATPG for scientific experiments. It was found to be non-toxic towards human cell lines and had no acute toxicity in mice. However, there is a need for further studies to evaluate the chronic toxicity of MATPG.

Applications in Scientific Experiments:

MATPG has potential applications in various fields of research, including medicinal chemistry, agriculture, and industry. It can be used as an analytical reagent for the analysis of various analytes. Furthermore, its antitumor and anti-inflammatory properties make it promising for the development of new drugs. Its inhibition of bacterial quorum sensing also makes it a potential candidate to develop novel antibiotics. Additionally, MATPG can be used in crop protection to increase plant resistance to pests and disease.

Current State of Research:

Currently, the research on MATPG is still at an early stage. Several studies have been conducted to evaluate its biological activities and applications in different fields. However, there is still a need for further studies to investigate its potential in drug development and agriculture.

Potential Implications in Various Fields of Research and Industry:

MATPG has potential implications in various fields such as agricultural biochemistry, drug development, and biotechnological industries. It can be used as a pesticide in crop protection and as an analytical reagent for the analysis of different analytes. Furthermore, its antitumor and anti-inflammatory properties make it promising in the development of new drugs, and its inhibition of bacterial quorum sensing could lead to the development of new antibiotics.

Limitations and Future Directions:

Although MATPG has shown promising results in various studies, several limitations and future directions need to be addressed. One of the limitations is the lack of information on its chronic toxicity. Further studies are required to evaluate its long-term effects on human health and the environment. Additionally, there is a need for more studies to investigate its potential applications in agriculture and industry. Future research could explore the feasibility of using MATPG for crop protection, as well as its potential as a biocatalyst in industrial processes.

List of Future Directions:

- Investigating the chronic toxicity of MATPG on living organisms

- Studying the efficacy of MATPG as a pesticide in crop protection

- Exploring the potential of MATPG as a biocatalyst in industrial processes

- Developing new analytical methods using MATPG for the analysis of different analytes

- Investigating the structural modifications of MATPG to enhance its biological activities and properties

- Developing new drugs using MATPG as a lead molecule

- Testing the potential use of MATPG as a drug carrier for targeted drug delivery

- Investigating the potential of MATPG as a biosensor for the detection of analytes

- Studying the mechanism of action of MATPG in different biological activities for a better understanding of its biological properties

- Investigating the potential of MATPG to be used in gene therapy.

CAS Number76101-13-8
Product NameMethyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-beta-D-glucopyranoside
IUPAC Name[(2R,3S,4R,5R,6R)-3,4-diacetyloxy-5-(1,3-dioxoisoindol-2-yl)-6-methoxyoxan-2-yl]methyl acetate
Molecular FormulaC21H23NO10
Molecular Weight449.41g/mol
InChIInChI=1S/C21H23NO10/c1-10(23)29-9-15-17(30-11(2)24)18(31-12(3)25)16(21(28-4)32-15)22-19(26)13-7-5-6-8-14(13)20(22)27/h5-8,15-18,21H,9H2,1-4H3/t15-,16-,17-,18-,21-/m1/s1
InChI KeyXNOVFZQMJSRWNJ-PDOZGGDVSA-N
SMILESCC(=O)OCC1C(C(C(C(O1)OC)N2C(=O)C3=CC=CC=C3C2=O)OC(=O)C)OC(=O)C
SynonymsMethyl 2-Deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-β-D-glucopyranoside 3,4,6-Triacetate; Methyl 2-Deoxy-2-phthalimido-β-D-glucopyranoside Triacetate;
Canonical SMILESCC(=O)OCC1C(C(C(C(O1)OC)N2C(=O)C3=CC=CC=C3C2=O)OC(=O)C)OC(=O)C
Isomeric SMILESCC(=O)OC[C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)OC)N2C(=O)C3=CC=CC=C3C2=O)OC(=O)C)OC(=O)C


CAS No: 76101-13-8 Synonyms: Methyl 2-deoxy-2-N-phthalimido-3,4,6-tri-O-acetyl-b-D-glucopyranoside MDL No: MFCD02683360 Chemical Formula: C21H23NO10 Molecular Weight: 449.41

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