| Identification | More | [Name]
N-Sulfo-glucosamine sodium salt | [CAS]
38899-05-7 | [Synonyms]
2-DEOXY-2-SULFAMINO-D-GLUCOPYRANOSE SODIUM SALT
2-Deoxy-2-(sulfoamino)-D-glucose monosodium salt
2-deoxy-2-sulfoamino-d-glucose sodium salt
D-GLUCOSAMINE-2-N-SULFATE, SODIUM SALT
D-GLUCOSAMINE-2-N-SULPHATE (NA)
D-GLUCOSAMINE 2-SULFATE SODIUM
D-GLUCOSAMINE 2-SULFATE SODIUM SALT
D-GLUCOSAMINE SULFATE SODIUM SALT
GLCN-2S, NA
GLUCOSAMINE SULFATE (SODIUM)
N-Sulfo-glucosamine sodium salt
D-Glucose, 2-deoxy-2-(sulfoamino)-, monosodium salt
2-deoxy-2-sulfamino-d-glucopyranose
D-Glucosamine-2-N-sulphatesodiumsalt
D-Dlucosamine sodium sulfate
D-Glucosamine Sulphate·2NaCl
Glucosamine Sulfate (D-Glucosamine Sulfate Disodium Chloride)
SODIUMSALT(6CI)
D-GLUCOSAMINE SULFATE SODIUM CHLORIDE
2-Deoxy-2-sulfamino-D-glucopyranose, GlcN-2S | [EINECS(EC#)]
609-596-2 | [Molecular Formula]
C6H12NNaO8S | [MDL Number]
MFCD00057972 | [Molecular Weight]
281.22 | [MOL File]
38899-05-7.mol |
| Hazard Information | Back Directory | [Description]
N-Sulfo-glucosamine sodium salt 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 it 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. | [Chemical Properties]
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