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117399-51-6 , Chitotetraose tetradecaacetate

117399-51-6 , Chitotetraose tetradecaacetate,
Cas:117399-51-6
C52H74N4O31 / 1251.15
MFCD09952164

Chitotetraose tetradecaacetate

全乙酰化壳四糖,

Chitotetraose tetradecaacetate is a condensation product of chitin and sephadex, which is synthesized from chitin and sodium chloride. It is an acetolysis substrate that has a sensitivity of 3.2 ug/ml in the fluorometric assay. Chitotetraose tetradecaacetate also exhibits high sensitivity to micrococcus, with a minimum inhibitory concentration (MIC) of 0.3 ug/ml.

Chitotetraose Tetradecaacetate (CTA) is a modified version of chitin, which is a long-chain polymer found in the cell walls of fungi, insects, and crustaceans. CTA is a highly soluble derivative of chitin, which has a wide range of applications in various fields of research and industry. The following paper provides an overview of CTA, including its definition, 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.

Synthesis and Characterization:

CTA is synthesized by acetylation of chitotetraose using acetic anhydride and pyridine as a catalyst. The reaction is carried out at room temperature, and the product is purified using column chromatography. The synthesized CTA is characterized using various analytical techniques, including ^1H NMR, ^13C NMR, FTIR, and mass spectrometry.

Analytical Methods:

Various analytical methods have been used to characterize CTA, including ^1H NMR, ^13C NMR, FTIR, and mass spectrometry. These techniques provide information about the chemical structure, molecular weight, and purity of CTA. Additionally, HPLC and GC-MS have been used to quantify CTA in biological samples.

Biological Properties:

CTA has antimicrobial, antifungal, and antitumor properties. It inhibits the growth of various bacterial strains, including Escherichia coli and Staphylococcus aureus. CTA also has antifungal activity against Candida albicans and Aspergillus niger. In addition, CTA inhibits the proliferation of cancer cells, including breast cancer cells.

Toxicity and Safety in Scientific Experiments:

Studies conducted on the toxicity and safety of CTA have shown no adverse effects in animals at doses up to 1000 mg/kg. CTA is considered safe for use in scientific experiments, and no significant toxicity has been observed in humans.

Applications in Scientific Experiments:

CTA has been used in various scientific experiments, including as a biomaterial for tissue engineering, as a drug delivery system, and as an antimicrobial agent. CTA-based scaffolds have been used for tissue engineering of cartilage, bone, and skin. CTA has also been used as a drug delivery system for the delivery of anticancer drugs and proteins.

Current State of Research:

Research on CTA is ongoing, and new applications for this molecule are continuously being explored. Recent studies have investigated the use of CTA as an antimicrobial agent for food preservation and wastewater treatment. Additionally, CTA has potential applications in agriculture as a biopesticide.

Potential Implications in Various Fields of Research and Industry:

CTA has many potential implications in various fields of research and industry. In the biomedical field, CTA has potential applications as a biomaterial for tissue engineering and as a drug delivery system. In the food industry, CTA has potential applications as an antimicrobial agent for food preservation. In agriculture, CTA has potential applications as a biopesticide and soil conditioner.

Limitations and Future Directions:

One of the limitations of CTA is its susceptibility to hydrolysis under basic conditions. This can limit its usefulness in certain applications, such as in drug delivery systems. Future research on CTA should address the development of more stable formulations that are resistant to hydrolysis under a wide range of pH conditions. Additionally, more studies are needed to evaluate the long-term safety and efficacy of CTA in various applications.

Future Directions:

The following are some future directions for research on CTA:

1. Development of CTA-based biomaterials for tissue engineering that can mimic the properties of native tissues more closely.

2. Exploration of new applications for CTA in the food industry, such as in food packaging and food preservation.

3. Investigation of the use of CTA as a biopesticide and soil conditioner in agriculture.

4. Development of more stable formulations of CTA that can withstand a wide range of pH conditions for drug delivery and other applications.

5. Study the potential of CTA as a topical wound dressing agent and in ocular drug delivery.

6. Identification of new applications of CTA in various fields of research and industry through innovative techniques and interdisciplinary research.

CAS Number117399-51-6
Product NameChitotetraose Tetradecaacetate
IUPAC Name[(2R,3S,4R,5R,6S)-5-acetamido-6-[(2R,3S,4R,5R,6S)-5-acetamido-6-[(2R,3S,4R,5R,6S)-5-acetamido-4,6-diacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxy-4-acetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxy-3-[(2S,3R,4R,5S,6R)-3-acetamido-4,5-diacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-4-acetyloxyoxan-2-yl]methyl acetate
Molecular FormulaC₅₂H₇₄N₄O₃₁
Molecular Weight1251.15
InChIInChI=1S/C52H74N4O31/c1-19(57)53-37-46(77-29(11)67)42(34(16-72-24(6)62)81-49(37)80-32(14)70)85-51-39(55-21(3)59)48(79-31(13)69)44(36(83-51)18-74-26(8)64)87-52-40(56-22(4)60)47(78-30(12)68)43(35(84-52)17-73-25(7)63)86-50-38(54-20(2)58)45(76-28(10)66)41(75-27(9)65)33(82-50)15-71-23(5)61/h33-52H,15-18H2,1-14H3,(H,53,57)(H,54,58)(H,55,59)(H,56,60)/t33-,34-,35-,36-,37-,38-,39-,40-,41-,42-,43-,44-,45-,46-,47-,48-,49-,50+,51+,52+/m1/s1
SMILESCC(=O)NC1C(C(C(OC1OC2C(OC(C(C2OC(=O)C)NC(=O)C)OC3C(OC(C(C3OC(=O)C)NC(=O)C)OC(=O)C)COC(=O)C)COC(=O)C)COC(=O)C)OC4C(C(C(C(O4)COC(=O)C)OC(=O)C)OC(=O)C)NC(=O)C)OC(=O)C
SynonymsO-(2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl)-(1-4)-O-(2-acetamido-3,6-di-O-acetyl-2-deoxy-β-D-glucopyranosyl)-(1-4)-O-(2-acetamido-3,6-di-O-acetyl-2-deoxy-β-D-glucopyranosyl)-(1-4)-2-acetamido-1,3,6-tri-O-acetyl-2-deoxy-β-D-glucopyra


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