CAS 38899-05-7
:D-Glucose, 2-deoxy-2-(sulfoamino)-, sodium salt (1:1)
Description:
D-Glucose, 2-deoxy-2-(sulfoamino)-, sodium salt (1:1), with the CAS number 38899-05-7, is a derivative of glucose that features a sulfoamino group at the 2-position of the glucose molecule. This modification imparts unique properties to the compound, including enhanced solubility in aqueous solutions due to the presence of the sodium salt form. The sulfoamino group can also influence the compound's reactivity and biological interactions, potentially affecting its role in biochemical pathways. As a carbohydrate, it retains the basic structural characteristics of glucose, including its six-membered ring structure and the ability to participate in various chemical reactions typical of sugars, such as oxidation and reduction. This compound may be utilized in various applications, including research in biochemistry and pharmacology, particularly in studies related to carbohydrate metabolism and the development of therapeutic agents. Its specific characteristics, such as stability, reactivity, and biological activity, would depend on the conditions under which it is used.
Formula:C6H13NO8S·Na
InChI:InChI=1S/C6H13NO8S.Na/c8-1-3(7-16(13,14)15)5(11)6(12)4(10)2-9;/h1,3-7,9-12H,2H2,(H,13,14,15);/t3-,4+,5+,6+;/m0./s1
InChI key:InChIKey=WIHMWELZJKBECO-BTVCFUMJSA-N
SMILES:[C@H]([C@H]([C@@H]([C@@H](CO)O)O)O)(NS(=O)(=O)O)C=O.[Na]
Synonyms:- 2-Deoxy-2-sulfoamino-<span class="text-smallcaps">D</span>-glucose sodium salt
- <span class="text-smallcaps">D</span>-Glucose, 2-deoxy-2-(sulfoamino)-, monosodium salt
- <span class="text-smallcaps">D</span>-Glucose, 2-deoxy-2-(sulfoamino)-, sodium salt (1:1)
- D-Glucosamine Sulfate 2NaCl
- D-Glucose,2-deoxy-2-(sulfoamino)-, sodium salt (1:1)
- D-glucosamine sulfate sodium
- Glucosamine, N-sulfo-, sodium salt
- Hexose, 2-Deoxy-2-(Sulfoamino)-, Monosodium Salt
- N-Sulfo-Glucosamine Sodium Salt
- 2-Deoxy-2-sulfoamino-D-glucose sodium salt
- D-Glucose, 2-deoxy-2-(sulfoamino)-, monosodium salt
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Found 9 products.
GLUCOSAMINE SULFATE SODIUM CHLORIDE CRS
CAS:<p>GLUCOSAMINE SULFATE SODIUM CHLORIDE CRS</p>Formula:C6H13NNaO8SMolecular weight:282.2241D-Glucose, 2-deoxy-2-(sulfoamino)-, sodium salt (1:1)
CAS:Formula:C6H13NNaO8SPurity:95%Color and Shape:SolidMolecular weight:282.22412-Deoxy-2-sulfoamino-D-glucose sodium
CAS:2-Deoxy-2-sulfoamino-D-glucose sodiumPurity:≥95%Molecular weight:281.22g/molD-Glucosamine 2-sulfate sodium salt
CAS:Formula:C6H12NNaO8SPurity:≥ 95% (anhydrous basis)Color and Shape:White or almost white powderMolecular weight:281.222-Deoxy-2-sulfoamino-D-glucose sodium
CAS:<p>2-Deoxy-2-sulfoamino-D-glucose sodium (GlcN-2S) is possible to effect reaction at arthritis.</p>Formula:C6H12NNaO8SPurity:99.76%Color and Shape:SolidMolecular weight:281.22D-Glucosamine-2-N-sulfate sodium
CAS:<p>D-Glucosamine-2-N-sulfate sodium is a synthetic, high purity carbohydrate with a custom synthesis. It is an oligosaccharide that is also a sugar and a saccharide. The methylation of D-glucosamine 2-N-sulfate sodium can be achieved by glycosylation or click modification. Click modification is the addition of a carbon atom to the molecule through the reaction with an electrophile, such as N-hydroxysuccinimide ester. This modification can be used to introduce fluorine atoms into the molecules, which can improve their solubility and stability. The product has shown anti-inflammatory activities in animal models, which may be due to its ability to inhibit prostaglandin synthesis.</p>Formula:C6H12NNaO8SPurity:Min. 95 Area-%Color and Shape:White Off-White PowderMolecular weight:281.22 g/molSodium ((2R,3R,4S,5R)-3,4,5,6-tetrahydroxy-1-oxohexan-2-yl)sulfamate
CAS:Formula:C6H12NNaO8SPurity:95%;RGMolecular weight:281.21D-Glucosamine-2-N-Sulfate Sodium Salt
CAS:<p>Applications D-Glucosamine-2-N-sulfate sodium salt (cas# 38899-05-7) is a useful research chemical.<br></p>Formula:C6H13NO5·2ClNa·H2O4SColor and Shape:NeatMolecular weight:573.31
