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  • 66456-69-7 , GM4-Ganglioside
66456-69-7 , GM4-Ganglioside

66456-69-7 , GM4-Ganglioside

66456-69-7 , GM4-Ganglioside
Cas:66456-69-7
MFCD00673749

GM4-Ganglioside

GM4-Ganglioside is one of the important glycosphingolipids found in the nervous system of mammals. It is a sialylated glycosphingolipid, and it plays an important role in cell signaling. GM4-Ganglioside has been extensively studied for its potential applicability in various clinical and research fields. In this paper, we will explore the definition and background of GM4-Ganglioside, its 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, and limitations and future directions.

Definition and Background

GM4-Ganglioside is a sialylated glycosphingolipid and belongs to the ganglioside class of glycosphingolipids. Gangliosides are glycosphingolipids that contain sialic acid residues, and they are primarily located on the outer surface of the plasma membranes in neural tissues, where they play a vital role in cell-cell interactions and cell signaling.

Physical and Chemical Properties

GM4-Ganglioside is a glycosphingolipid with a complex molecular structure, consisting of a ceramide backbone that is linked to a carbohydrate moiety composed of a series of sugars and sialic acid residues. The structural composition of GM4-Ganglioside determines its physicochemical properties, including its solubility, stability, and reactivity.

Synthesis and Characterization

GM4-Ganglioside can be synthesized by chemical or enzymatic methods. The chemical synthesis of GM4-Ganglioside involves the stepwise construction of the ceramide backbone, followed by the addition of the sugar and sialic acid residues. The enzymatic synthesis of GM4-Ganglioside involves the use of specific glycosyltransferases and sialyltransferases to transfer the corresponding sugar and sialic acid residues to the ceramide backbone.

Analytical Methods

Several analytical methods have been developed for the detection and quantification of GM4-Ganglioside, including high-performance liquid chromatography (HPLC), mass spectrometry (MS), nuclear magnetic resonance (NMR), and enzyme-linked immunosorbent assay (ELISA).

Biological Properties

GM4-Ganglioside has been reported to play a crucial role in various biological processes, including cell differentiation, cell proliferation, apoptosis, and neuronal development. GM4-Ganglioside has also been implicated in several pathological conditions, including neurodegeneration and cancer.

Toxicity and Safety in Scientific Experiments

The toxicity and safety of GM4-Ganglioside in scientific experiments depend on the concentration and exposure time. GM4-Ganglioside has been reported to be cytotoxic to certain cell lines at high concentrations. However, several in vivo and in vitro studies have shown that GM4-Ganglioside is safe for therapeutic use at lower concentrations.

Applications in Scientific Experiments

GM4-Ganglioside has been extensively studied for its potential applications in various areas of research and industry, including neuroscience, oncology, and nanotechnology. GM4-Ganglioside has been reported to have neuroprotective, antitumor, immunomodulatory, and antimicrobial properties.

Current State of Research

The current state of research on GM4-Ganglioside is focused on elucidating its molecular mechanisms of action, identifying its therapeutic potential for various clinical conditions, and developing novel methods for its synthesis and characterization.

Potential Implications in Various Fields of Research and Industry

GM4-Ganglioside has potential implications in various fields of research and industry, including neuroscience, oncology, and nanotechnology. In neuroscience, GM4-Ganglioside may have therapeutic potential for neurodegenerative diseases, such as Alzheimer's and Parkinson's diseases. In oncology, GM4-Ganglioside may have potential as a target for cancer immunotherapy. In nanotechnology, GM4-Ganglioside may have potential for the development of drug delivery systems.

Limitations and Future Directions

Despite the promising therapeutic potential of GM4-Ganglioside, several limitations and future directions need to be considered. One limitation is the poor bioavailability and pharmacokinetic properties of GM4-Ganglioside, which may limit its therapeutic efficacy. Another limitation is the potential toxicity and adverse effects of GM4-Ganglioside, which need to be further evaluated. Future directions include developing novel methods for the synthesis and characterization of GM4-Ganglioside, investigating its molecular mechanisms of action, and exploring its therapeutic potential for various clinical conditions.

Future directions:

1. Developing new synthetic strategies to enhance the yield and purity of GM4-Ganglioside.

2. Investigating the molecular mechanisms underlying the neuroprotective effects of GM4-Ganglioside.

3. Developing new drug delivery systems based on GM4-Ganglioside for improved bioavailability and targeted delivery.

4. Exploring the potential of GM4-Ganglioside as a therapeutic target for autoimmunity.

5. Evaluating the role of GM4-Ganglioside in modulating the immune response to infections.

6. Investigating the potential use of GM4-Ganglioside as a biomarker for neurodegenerative diseases.

7. Exploring the role of GM4-Ganglioside in neuronal plasticity and learning and memory.

8. Developing new analytical methods for the detection and quantification of GM4-Ganglioside.

9. Investigating the potential of GM4-Ganglioside as a therapeutic target for cancer immunotherapy.

10. Exploring the use of GM4-Ganglioside in the development of novel biomaterials for tissue engineering.

CAS Number66456-69-7
Product NameGM4-Ganglioside
IUPAC NameN-[2-[(2R,3R,4S,5S,6R)-4-[(2R,4S,5R,6R)-5-acetamido-4-hydroxy-6-[(1S,2R)-1,2,3-trihydroxypropyl]oxan-2-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]octadecanamide
Molecular FormulaC36H68N2O13
Molecular Weight736.941
InChIInChI=1S/C36H68N2O13/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-28(44)37-19-20-48-36-33(47)35(32(46)27(23-40)49-36)51-29-21-25(42)30(38-24(2)41)34(50-29)31(45)26(43)22-39/h25-27,29-36,39-40,42-43,45-47H,3-23H2,1-2H3,(H,37,44)(H,38,41)/t25-,26+,27+,29+,30+,31-,32-,33+,34+,35-,36+/m0/s1
InChI KeyHHWCOPBSANJMBY-IBIJVICQSA-N
SMILESCCCCCCCCCCCCCCCCCC(=O)NCCOC1C(C(C(C(O1)CO)O)OC2CC(C(C(O2)C(C(CO)O)O)NC(=O)C)O)O
SynonymsGM4


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