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  • 19600-01-2 , GM2-Ganglioside , Monosialoganglioside GM2
19600-01-2 , GM2-Ganglioside , Monosialoganglioside GM2

19600-01-2 , GM2-Ganglioside , Monosialoganglioside GM2

19600-01-2 , GM2-Ganglioside ,
Monosialoganglioside GM2;
b-GalNAc-(1→4)-[a-Neu5Ac-(2→3)]-b-Gal(1→4)-b-Glc-(1→1')-Cer
Cas:19600-01-2
C67H121N3O26 / 1384.68

GM2-Ganglioside , Monosialoganglioside GM2; 

b-GalNAc-(1→4)-[a-Neu5Ac-(2→3)]-b-Gal(1→4)-b-Glc-(1→1')-Cer

Gangliosides are sialic acid-containing glycosphingolipids that are abundantly found in the nervous system and other organs. They play a crucial role in several cellular processes, including cell growth, differentiation, signaling, and adhesion. Ganglioside GM2 is a member of the ganglioside family, which contains a sialic acid residue linked to a lactosylceramide backbone. In this paper, we will provide a comprehensive review of Ganglioside GM2 Sodium Salt, including its definition, physical and chemical properties, synthesis, analytical methods, biological properties, toxicity, safety, applications, current state of research, potential implications, limitations, and future directions.

Definition and Background:

Ganglioside GM2 Sodium Salt is a synthetic form of ganglioside GM2 that is obtained by chemical modification of natural gangliosides. It has a similar structure to natural gangliosides and exhibits similar biological properties. It has been extensively studied for its potential use in several fields, including neuroscience, immunology, and cancer research.

Synthesis and Characterization:

Ganglioside GM2 Sodium Salt is synthesized by chemical modification of natural gangliosides, such as bovine brain gangliosides. The most common method of synthesis involves chemical acetylation of natural gangliosides, followed by deacetylation and subsequent saponification. The resulting product is then purified by various chromatographic techniques, such as silica gel chromatography, ion exchange chromatography, or gel filtration chromatography.

Analytical Methods:

Several analytical methods have been used to identify and characterize Ganglioside GM2 Sodium Salt, including mass spectrometry, nuclear magnetic resonance spectroscopy, and high-performance thin-layer chromatography. These techniques help to confirm the purity and identity of the compound.

Biological Properties:

Ganglioside GM2 Sodium Salt has several biological properties that make it an attractive target for research. It has been shown to play a critical role in cell adhesion, migration, and signaling. It also has potential applications in neuroscience, cancer research, and immunology.

Toxicity and Safety in Scientific Experiments:

Ganglioside GM2 Sodium Salt has been extensively studied for its safety in scientific experiments. It has been shown to have low toxicity and high tolerability in animals and humans. However, it is important to note that the toxicity and safety of this compound may vary depending on the dosage and administration route.

Applications in Scientific Experiments:

Ganglioside GM2 Sodium Salt has several potential applications in scientific experiments, including neuroregeneration, cancer therapy, and immunotherapy. It has been shown to promote the survival and growth of neurons in vitro and in vivo. It also has potential as a therapeutic agent for certain types of cancer and as an adjuvant for immunotherapy.

Current State of Research:

The current state of research on Ganglioside GM2 Sodium Salt is promising. Several studies have demonstrated its potential applications in neuroscience, cancer research, and immunology. However, further research is needed to fully understand its biological mechanisms and potential therapeutic applications.

Potential Implications in Various Fields of Research and Industry:

The potential implications of Ganglioside GM2 Sodium Salt in various fields of research and industry are vast. It has potential applications in neuroscience, cancer research, and immunology. It could be used as a therapeutic agent for certain types of cancer and as an adjuvant for immunotherapy. In addition, it could be used to promote neuroregeneration and as a treatment for neurodegenerative diseases.

Limitations and Future Directions:

Despite the promising potential of Ganglioside GM2 Sodium Salt, there are several limitations that must be addressed in future research. These include the need for further studies to determine the optimal dosage, administration route, and treatment duration. There is also a need for further research to fully understand its biological mechanisms of action and potential adverse effects. Future research should focus on addressing these limitations and exploring new avenues for research.

Future Directions:

There are several possible future directions for research on Ganglioside GM2 Sodium Salt. These include:

1. Development of new synthesis methods to improve purity and yield

2. Investigation of its potential applications in the treatment of neurodegenerative diseases, such as Alzheimer's and Parkinson's disease

3. Examination of its potential as a therapeutic agent for infectious diseases and autoimmune disorders

4. Study of its role in the regulation of the immune system and its potential as an immunomodulatory agent

5. Investigation of its potential applications in tissue engineering and regenerative medicine.

Conclusion:

In conclusion, Ganglioside GM2 Sodium Salt is a promising compound with several potential applications in various fields of research and industry. It has been extensively studied for its biological properties, toxicity, and safety in scientific experiments. However, further research is needed to fully understand its mechanisms of action and potential therapeutic applications. The limitations and future directions discussed in this paper provide valuable insights into the potential of Ganglioside GM2 Sodium Salt as a therapeutic agent and highlight the need for additional research in this area.

CAS Number19600-01-2
Product NameGANGLIOSIDE GM2 SODIUM SALT
IUPAC Name(2R,4R,5S,6S)-5-acetamido-2-[[(2R,3S,4S,5R,6S)-5-[(2R,3S,4S,5S,6S)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(E,2R,3S)-3-hydroxy-2-(octadecanoylamino)octadec-4-enoxy]oxan-3-yl]oxy-3-hydroxy-6-(hydroxymethyl)oxan-4-yl]oxymethyl]-4-hydroxy-6-[(1S,2S)-1,2,3-trihydroxypropyl]oxane-2-carboxylic acid
Molecular FormulaC68H123N3O26
Molecular Weight1398.727
InChIInChI=1S/C68H123N3O26/c1-5-7-9-11-13-15-17-19-20-22-24-26-28-30-32-34-51(81)71-44(45(78)33-31-29-27-25-23-21-18-16-14-12-10-8-6-2)40-90-65-58(86)57(85)60(49(38-74)93-65)95-66-59(87)63(61(50(39-75)94-66)96-64-53(70-43(4)77)56(84)55(83)48(37-73)92-64)91-41-68(67(88)89)35-46(79)52(69-42(3)76)62(97-68)54(82)47(80)36-72/h31,33,44-50,52-66,72-75,78-80,82-87H,5-30,32,34-41H2,1-4H3,(H,69,76)(H,70,77)(H,71,81)(H,88,89)/b33-31+/t44-,45+,46-,47+,48+,49+,50+,52+,53+,54+,55-,56+,57+,58+,59+,60+,61-,62+,63+,64-,65-,66-,68-/m1/s1
InChI KeyUSMMPBVNWHAJBE-YMEOXFOQSA-N
SMILESCCCCCCCCCCCCCCCCCC(=O)NC(COC1C(C(C(C(O1)CO)OC2C(C(C(C(O2)CO)OC3C(C(C(C(O3)CO)O)O)NC(=O)C)OCC4(CC(C(C(O4)C(C(CO)O)O)NC(=O)C)O)C(=O)O)O)O)O)C(C=CCCCCCCCCCCCCC)O


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