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  • 74135-10-7 , 蔗糖八硫酸酯钠盐, CAS:74135-10-7
  • 74135-10-7 , 蔗糖八硫酸酯钠盐, CAS:74135-10-7
74135-10-7 , 蔗糖八硫酸酯钠盐, CAS:74135-10-774135-10-7 , 蔗糖八硫酸酯钠盐, CAS:74135-10-7

74135-10-7 , 蔗糖八硫酸酯钠盐, CAS:74135-10-7

74135-10-7 , Sucrose octasulfate sodium salt,
蔗糖八硫酸酯钠盐,
CAS:74135-10-7
C12H14Na8O35S8 / 1158.66
MFCD00933758

蔗糖八硫酸酯钠盐

Sucrose octasulfate sodium salt

This compound is generally known as sucralfates and are medications primarily taken to treat active duodenal ulcers. They are also used for the treatment of gastroesophageal reflux disease (GERD) and stress ulcers.  Sucralfate is a sucrose sulfate-aluminium complex that binds to the ulcer, creating a physical barrier that protects the gastrointestinal tract from stomach acid and prevents the degradation of mucus. It also promotes bicarbonate production and acts like an acid buffer with cytoprotective properties.

Sucrose octasulfate sodium salt is a synthetic compound that has attracted significant attention as naturally occurring sulfated polysaccharides have been found to exhibit various biological activities. It is water-soluble, anionic and is known to be stable at various pHs.

Definition and Background:

Sucrose octasulfate sodium salt is a synthetic compound of sucrose and sulfuric acid, where eight sulfate groups are present on the sugar molecule. The compound has been used in biomedical research to study various biological processes. It is known to show anticoagulant activity and may play a role in inflammation.

Synthesis and Characterization:

Sucrose octasulfate sodium salt is synthesized by reacting sucrose with sulfur trioxide in the presence of a solvent. The synthesized product is then purified by either column chromatography, ion exchange chromatography, or gel filtration. The structure is characterized by NMR, elemental analysis, and other analytical techniques.

Analytical Methods:

Analytical methods such as ion chromatography, thin-layer chromatography, HPLC, and spectrophotometry are used to determine the purity and degree of sulfation of sucrose octasulfate sodium salt. These techniques allow scientists to monitor and control the quality of the product during synthesis and ensure that it is suitable for use in experiments.

Biological Properties:

Sucrose octasulfate sodium salt has been shown to exhibit anticoagulant activity by inhibiting the activity of thrombin and factor Xa. The compound also possesses anti-inflammatory properties by inhibiting the production of pro-inflammatory cytokines. It has also been shown to play crucial roles in cell signaling, platelet aggregation, and angiogenesis.

Toxicity and Safety in Scientific Experiments:

Studies have shown that sucrose octasulfate sodium salt is non-toxic and has low systemic toxicity when administered to animals. However, the compound should always be handled with care as it may irritate the skin and mucous membranes. In experiments, its toxicity should be evaluated by conducting cytotoxicity assays before use.

Applications in Scientific Experiments:

Sucrose octasulfate sodium salt has a wide range of applications in various fields of research, including coagulation, inflammation, cancer, and angiogenesis. The compound is also commonly used in the study of cell signaling and molecular mechanisms of biological processes.

Current State of Research:

Recent studies have shown the potential of sucrose octasulfate sodium salt as a therapeutic agent in the treatment of various diseases such as cancer, thrombosis, and inflammation. Moreover, it has been shown to play a crucial role in wound healing and tissue regeneration.

Potential Implications in Various Fields of Research and Industry:

Sucrose octasulfate sodium salt holds potential in a wide range of fields including biomedical research, drug discovery, and nanotechnology. It is also used in the cosmetic industry as an ingredient in anti-aging creams and lotions.

Limitations:

One limitation of sucrose octasulfate sodium salt is its stability at various temperatures, which can complicate storage and handling. Moreover, despite being a promising therapeutic agent, its clinical applications remain limited due to a lack of conducted clinical trials.

Future Directions:

Future directions include exploring the role of sucrose octasulfate sodium salt in tissue engineering and regenerative medicine. Further studies will be necessary to assess its safety and efficacy as a therapeutic agent in humans. Other promising applications include its use in drug delivery systems and nanomedicine. Finally, it will be essential to continue to explore the potential of this compound in other fields of research, such as cancer immunotherapy and inflammatory diseases.

CAS Number74135-10-7
Product NameSucrose octasulfate sodium salt
IUPAC Nameoctasodium;[(2R,3R,4S,5R,6R)-2-[(2S,3S,4R,5R)-3,4-disulfonatooxy-2,5-bis(sulfonatooxymethyl)oxolan-2-yl]oxy-3,5-disulfonatooxy-6-(sulfonatooxymethyl)oxan-4-yl] sulfate
Molecular FormulaC12H14Na8O35S8
Molecular Weight1158.66 g/mol
InChIInChI=1S/C12H22O35S8.8Na/c13-48(14,15)37-1-4-6(43-51(22,23)24)8(45-53(28,29)30)9(46-54(31,32)33)11(40-4)42-12(3-39-50(19,20)21)10(47-55(34,35)36)7(44-52(25,26)27)5(41-12)2-38-49(16,17)18;;;;;;;;/h4-11H,1-3H2,(H,13,14,15)(H,16,17,18)(H,19,20,21)(H,22,23,24)(H,25,26,27)(H,28,29,30)(H,31,32,33)(H,34,35,36);;;;;;;;/q;8*+1/p-8/t4-,5-,6-,7-,8+,9-,10+,11-,12+;;;;;;;;/m1......../s1
InChI KeyCPRSOZZDECJZKH-QRDGSJRXSA-F
SMILESC(C1C(C(C(C(O1)OC2(C(C(C(O2)COS(=O)(=O)[O-])OS(=O)(=O)[O-])OS(=O)(=O)[O-])COS(=O)(=O)[O-])OS(=O)(=O)[O-])OS(=O)(=O)[O-])OS(=O)(=O)[O-])OS(=O)(=O)[O-].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+]
Synonyms1,3,4,6-Tetra-O-sulfo-β-D-fructofuranosyl α-D-Glucopyranoside 2,3,4,6-Tetrakis(hydrogen sulfate) Sodium Salt; Sodium Sucrose Octasulfate;
Canonical SMILESC(C1C(C(C(C(O1)OC2(C(C(C(O2)COS(=O)(=O)[O-])OS(=O)(=O)[O-])OS(=O)(=O)[O-])COS(=O)(=O)[O-])OS(=O)(=O)[O-])OS(=O)(=O)[O-])OS(=O)(=O)[O-])OS(=O)(=O)[O-].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+]
Isomeric SMILESC([C@@H]1[C@H]([C@@H]([C@H]([C@H](O1)O[C@]2([C@H]([C@@H]([C@H](O2)COS(=O)(=O)[O-])OS(=O)(=O)[O-])OS(=O)(=O)[O-])COS(=O)(=O)[O-])OS(=O)(=O)[O-])OS(=O)(=O)[O-])OS(=O)(=O)[O-])OS(=O)(=O)[O-].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+]


CAS No: 127930-09-0,74135-10-7 Synonyms: 1,3,4,6-Tetra-O-sulfo-b-D-fructofuranosyl-2,3,4,6-tetrakis(hydrogen sulfate)-a-D-glucopyranoside sodium salt MDL No: MFCD00933758 Chemical Formula: C12H14Na8O35S8 Molecular Weight: 1158.66

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